Carrel name: keyword-pbs-cord Creating study carrel named keyword-pbs-cord Initializing database file: cache/cord-002013-rb9xdzro.json key: cord-002013-rb9xdzro authors: Zheng, Xuexing; Wong, Gary; Zhao, Yongkun; Wang, Hualei; He, Shihua; Bi, Yuhai; Chen, Weijin; Jin, Hongli; Gai, Weiwei; Chu, Di; Cao, Zengguo; Wang, Chong; Fan, Quanshui; Chi, Hang; Gao, Yuwei; Wang, Tiecheng; Feng, Na; Yan, Feihu; Huang, Geng; Zheng, Ying; Li, Nan; Li, Yuetao; Qian, Jun; Zou, Yong; Kobinger, Gary; Gao, George Fu; Qiu, Xiangguo; Yang, Songtao; Xia, Xianzhu title: Treatment with hyperimmune equine immunoglobulin or immunoglobulin fragments completely protects rodents from Ebola virus infection date: 2016-04-12 journal: Sci Rep DOI: 10.1038/srep24179 sha: doc_id: 2013 cord_uid: rb9xdzro file: cache/cord-003915-kje8lvgl.json key: cord-003915-kje8lvgl authors: Pigeyre, Laetitia; Schatz, Malvina; Ravallec, Marc; Gasmi, Leila; Nègre, Nicolas; Clouet, Cécile; Seveno, Martial; El Koulali, Khadija; Decourcelle, Mathilde; Guerardel, Yann; Cot, Didier; Dupressoir, Thierry; Gosselin-Grenet, Anne-Sophie; Ogliastro, Mylène title: Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda date: 2019-09-17 journal: Viruses DOI: 10.3390/v11090870 sha: doc_id: 3915 cord_uid: kje8lvgl file: cache/cord-001732-4eyn7pjq.json key: cord-001732-4eyn7pjq authors: Riede, O; Seifert, K; Oswald, D; Endmann, A; Hock, C; Winkler, A; Salguero, F J; Schroff, M; Croft, S L; Juhls, C title: Preclinical safety and tolerability of a repeatedly administered human leishmaniasis DNA vaccine date: 2015-04-30 journal: Gene Ther DOI: 10.1038/gt.2015.35 sha: doc_id: 1732 cord_uid: 4eyn7pjq file: cache/cord-001017-4qfhltg4.json key: cord-001017-4qfhltg4 authors: Chatterjee, Dhriti; Biswas, Kaushiki; Nag, Soma; Ramachandra, S. G.; Das Sarma, Jayasri title: Microglia Play a Major Role in Direct Viral-Induced Demyelination date: 2013-06-20 journal: Clin Dev Immunol DOI: 10.1155/2013/510396 sha: doc_id: 1017 cord_uid: 4qfhltg4 file: cache/cord-011106-h20vbmbo.json key: cord-011106-h20vbmbo authors: Takeda, Yohei; Okuyama, Yuko; Nakano, Hiroto; Yaoita, Yasunori; Machida, Koich; Ogawa, Haruko; Imai, Kunitoshi title: Antiviral Activities of Hibiscus sabdariffa L. Tea Extract Against Human Influenza A Virus Rely Largely on Acidic pH but Partially on a Low-pH-Independent Mechanism date: 2019-10-16 journal: Food Environ Virol DOI: 10.1007/s12560-019-09408-x sha: doc_id: 11106 cord_uid: h20vbmbo file: cache/cord-013526-6fip93l2.json key: cord-013526-6fip93l2 authors: Labadie, Thomas; Roy, Polly title: A non-enveloped arbovirus released in lysosome-derived extracellular vesicles induces super-infection exclusion date: 2020-10-19 journal: PLoS Pathog DOI: 10.1371/journal.ppat.1009015 sha: doc_id: 13526 cord_uid: 6fip93l2 file: cache/cord-009800-tajkpgkj.json key: cord-009800-tajkpgkj authors: Orellana, Mhica V.; Perry, Mary Jane title: An immunoprobe to measure Rubisco concentrations and maximal photosynthetic rates of individual phytoplankton cells date: 2003-12-22 journal: Limnol Oceanogr DOI: 10.4319/lo.1992.37.3.0478 sha: doc_id: 9800 cord_uid: tajkpgkj file: cache/cord-001065-j4hvyyoi.json key: cord-001065-j4hvyyoi authors: Boncristiani, Humberto F.; Evans, Jay D.; Chen, Yanping; Pettis, Jeff; Murphy, Charles; Lopez, Dawn L.; Simone-Finstrom, Michael; Strand, Micheline; Tarpy, David R.; Rueppell, Olav title: In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) date: 2013-09-05 journal: PLoS One DOI: 10.1371/journal.pone.0073429 sha: doc_id: 1065 cord_uid: j4hvyyoi file: cache/cord-267736-rya9w6sh.json key: cord-267736-rya9w6sh authors: Kang, Xiaoping; Li, Yuchang; Fan, Li; Lin, Fang; Wei, Jingjing; Zhu, Xiaolei; Hu, Yi; Li, Jing; Chang, Guohui; Zhu, Qingyu; Liu, Hong; Yang, Yinhui title: Development of an ELISA-array for simultaneous detection of five encephalitis viruses date: 2012-02-27 journal: Virol J DOI: 10.1186/1743-422x-9-56 sha: doc_id: 267736 cord_uid: rya9w6sh file: cache/cord-000354-05lnj3w0.json key: cord-000354-05lnj3w0 authors: de Vries, Erik; Tscherne, Donna M.; Wienholts, Marleen J.; Cobos-Jiménez, Viviana; Scholte, Florine; García-Sastre, Adolfo; Rottier, Peter J. M.; de Haan, Cornelis A. M. title: Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway date: 2011-03-31 journal: PLoS Pathog DOI: 10.1371/journal.ppat.1001329 sha: doc_id: 354 cord_uid: 05lnj3w0 file: cache/cord-013265-qrfi6e5c.json key: cord-013265-qrfi6e5c authors: Isono, Toshihito; Domon, Hisanori; Nagai, Kosuke; Maekawa, Tomoki; Tamura, Hikaru; Hiyoshi, Takumi; Yanagihara, Katsunori; Kunitomo, Eiji; Takenaka, Shoji; Noiri, Yuichiro; Terao, Yutaka title: Treatment of severe pneumonia by hinokitiol in a murine antimicrobial-resistant pneumococcal pneumonia model date: 2020-10-15 journal: PLoS One DOI: 10.1371/journal.pone.0240329 sha: doc_id: 13265 cord_uid: qrfi6e5c file: cache/cord-002583-cgcf7mgj.json key: cord-002583-cgcf7mgj authors: Zhuo, Xun-hui; Sun, Hong-chao; Huang, Bin; Yu, Hai-jie; Shan, Ying; Du, Ai-fang title: Evaluation of potential anti-toxoplasmosis efficiency of combined traditional herbs in a mouse model date: 2017-06-01 journal: Journal of Zhejiang University-SCIENCE B DOI: 10.1631/jzus.b1600316 sha: doc_id: 2583 cord_uid: cgcf7mgj file: cache/cord-275635-d50bxe7c.json key: cord-275635-d50bxe7c authors: Yuan, Xiaomin; Lin, Huixing; Fan, Hongjie title: Efficacy and immunogenicity of recombinant swinepox virus expressing the A epitope of the TGEV S protein date: 2015-07-31 journal: Vaccine DOI: 10.1016/j.vaccine.2015.06.057 sha: doc_id: 275635 cord_uid: d50bxe7c file: cache/cord-026866-0hlre9i6.json key: cord-026866-0hlre9i6 authors: Perruzza, Lisa; Jaconi, Stefano; Lombardo, Gloria; Pinna, Debora; Strati, Francesco; Morone, Diego; Seehusen, Frauke; Hu, Yue; Bajoria, Sakshi; Xiong, Jian; Kumru, Ozan Selahattin; Joshi, Sangeeta Bagai; Volkin, David Bernard; Piantanida, Renato; Benigni, Fabio; Grassi, Fabio; Corti, Davide; Pizzuto, Matteo Samuele title: Prophylactic Activity of Orally Administered FliD-Reactive Monoclonal SIgA Against Campylobacter Infection date: 2020-06-09 journal: Front Immunol DOI: 10.3389/fimmu.2020.01011 sha: doc_id: 26866 cord_uid: 0hlre9i6 file: cache/cord-259094-5qzbctan.json key: cord-259094-5qzbctan authors: Xu, Mei Ling; Kim, Hyoung Jin; Chang, Don Yong; Kim, Hong-Jin title: The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection date: 2013-04-26 journal: J Microbiol DOI: 10.1007/s12275-013-2683-y sha: doc_id: 259094 cord_uid: 5qzbctan file: cache/cord-259364-8zoav7b0.json key: cord-259364-8zoav7b0 authors: Xiao, Yire; Hu, Qingqing; Jiao, Luoying; Cui, Xiping; Wu, Panpan; He, Pan; Xia, Nana; Lv, Rui; Liang, Yuxin; Zhao, Suqing title: Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis date: 2019-09-09 journal: Microb Pathog DOI: 10.1016/j.micpath.2019.103741 sha: doc_id: 259364 cord_uid: 8zoav7b0 file: cache/cord-264267-weat0qs6.json key: cord-264267-weat0qs6 authors: Kleine-Weber, Hannah; Schroeder, Simon; Krüger, Nadine; Prokscha, Alexander; Naim, Hassan Y.; Müller, Marcel A.; Drosten, Christian; Pöhlmann, Stefan; Hoffmann, Markus title: Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus date: 2020-01-21 journal: Emerg Microbes Infect DOI: 10.1080/22221751.2020.1713705 sha: doc_id: 264267 cord_uid: weat0qs6 file: cache/cord-295416-y3lvcjqd.json key: cord-295416-y3lvcjqd authors: Eichinger, Katherine M.; Kosanovich, Jessica L.; Gidwani, Sonal V.; Zomback, Aaron; Lipp, Madeline A.; Perkins, Timothy N.; Oury, Tim D.; Petrovsky, Nikolai; Marshall, Christopher P.; Yondola, Mark A.; Empey, Kerry M. title: Prefusion RSV F Immunization Elicits Th2-Mediated Lung Pathology in Mice When Formulated With a Th2 (but Not a Th1/Th2-Balanced) Adjuvant Despite Complete Viral Protection date: 2020-07-29 journal: Front Immunol DOI: 10.3389/fimmu.2020.01673 sha: doc_id: 295416 cord_uid: y3lvcjqd file: cache/cord-338108-3rn6fwx3.json key: cord-338108-3rn6fwx3 authors: Jin, Yi; Zhang, Yuewei; Wan, Chunyan; Wang, Hongjun; Hou, Lingyu; Chang, Jianyu; Fan, Kai; Xie, Xiangming title: Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection date: 2013-09-18 journal: Evid Based Complement Alternat Med DOI: 10.1155/2013/194976 sha: doc_id: 338108 cord_uid: 3rn6fwx3 file: cache/cord-274396-l611eisi.json key: cord-274396-l611eisi authors: Park, Su-Jin; Yu, Kwang-Min; Kim, Young-Il; Kim, Se-Mi; Kim, Eun-Ha; Kim, Seong-Gyu; Kim, Eun Ji; Casel, Mark Anthony B.; Rollon, Rare; Jang, Seung-Gyu; Lee, Min-Hyeok; Chang, Jae-Hyung; Song, Min-Suk; Jeong, Hye Won; Choi, Younho; Chen, Weiqiang; Shin, Woo-Jin; Jung, Jae U.; Choi, Young Ki title: Antiviral Efficacies of FDA-Approved Drugs against SARS-CoV-2 Infection in Ferrets date: 2020-05-22 journal: mBio DOI: 10.1128/mbio.01114-20 sha: doc_id: 274396 cord_uid: l611eisi file: cache/cord-308461-4lhh3du0.json key: cord-308461-4lhh3du0 authors: Ueki, Hiroshi; Wang, I-Hsuan; Zhao, Dongming; Gunzer, Matthias; Kawaoka, Yoshihiro title: Multicolor two-photon imaging of in vivo cellular pathophysiology upon influenza virus infection using the two-photon IMPRESS date: 2020-01-29 journal: Nat Protoc DOI: 10.1038/s41596-019-0275-y sha: doc_id: 308461 cord_uid: 4lhh3du0 file: cache/cord-335310-61wibso4.json key: cord-335310-61wibso4 authors: Chen, Hui-Wen; Huang, Chen-Yu; Lin, Shu-Yi; Fang, Zih-Syun; Hsu, Chen-Hsuan; Lin, Jung-Chen; Chen, Yuan-I; Yao, Bing-Yu; Hu, Che-Ming J. title: Synthetic virus-like particles prepared via protein corona formation enable effective vaccination in an avian model of coronavirus infection date: 2016-08-15 journal: Biomaterials DOI: 10.1016/j.biomaterials.2016.08.018 sha: doc_id: 335310 cord_uid: 61wibso4 file: cache/cord-309742-fd1qmr87.json key: cord-309742-fd1qmr87 authors: Slepushkin, Vladimir A.; Staber, Patrick D.; Wang, Guoshun; McCray, Paul B.; Davidson, Beverly L. title: Infection of Human Airway Epithelia with H1N1, H2N2, and H3N2 Influenza A Virus Strains date: 2016-12-14 journal: Mol Ther DOI: 10.1006/mthe.2001.0277 sha: doc_id: 309742 cord_uid: fd1qmr87 file: cache/cord-303381-xvzhb7ix.json key: cord-303381-xvzhb7ix authors: TSURUTA, Yuya; SHIBUTANI, Shusaku T.; WATANABE, Rie; IWATA, Hiroyuki title: The requirement of environmental acidification for Ibaraki virus infection to host cells date: 2015-08-28 journal: J Vet Med Sci DOI: 10.1292/jvms.15-0222 sha: doc_id: 303381 cord_uid: xvzhb7ix file: cache/cord-278802-bverdk5w.json key: cord-278802-bverdk5w authors: Zhou, Yefei; Zhou, Meixian; Zhang, Dunlin; Zhang, Honglin; Zhang, Liyang title: Immune response of AA broilers to IBV H120 vaccine and sodium new houttuyfonate date: 2010-12-31 journal: Research in Veterinary Science DOI: 10.1016/j.rvsc.2010.04.010 sha: doc_id: 278802 cord_uid: bverdk5w file: cache/cord-276732-u2d1z4ip.json key: cord-276732-u2d1z4ip authors: Mauri, Tommaso; Zambelli, Vanessa; Cappuzzello, Claudia; Bellani, Giacomo; Dander, Erica; Sironi, Marina; Castiglioni, Vittoria; Doni, Andrea; Mantovani, Alberto; Biondi, Andrea; Garlanda, Cecilia; D’amico, Giovanna; Pesenti, Antonio title: Intraperitoneal adoptive transfer of mesenchymal stem cells enhances recovery from acid aspiration acute lung injury in mice date: 2017-03-06 journal: Intensive Care Med Exp DOI: 10.1186/s40635-017-0126-5 sha: doc_id: 276732 cord_uid: u2d1z4ip file: cache/cord-260834-v254de8k.json key: cord-260834-v254de8k authors: Lim, Chia Chiu; Woo, Patrick C. Y.; Lim, Theam Soon title: Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies date: 2019-04-15 journal: Sci Rep DOI: 10.1038/s41598-019-42628-6 sha: doc_id: 260834 cord_uid: v254de8k file: cache/cord-277054-eq4obbte.json key: cord-277054-eq4obbte authors: Kaur, Manpreet; Rai, Anant; Bhatnagar, Rakesh title: Rabies DNA vaccine: No impact of MHC Class I and Class II targeting sequences on immune response and protection against lethal challenge date: 2009-03-26 journal: Vaccine DOI: 10.1016/j.vaccine.2009.01.128 sha: doc_id: 277054 cord_uid: eq4obbte file: cache/cord-273035-sewfb3q8.json key: cord-273035-sewfb3q8 authors: Kang, Xixiong; Xu, Yang; Wu, Xiaoyi; Liang, Yong; Wang, Chen; Guo, Junhua; Wang, Yajie; Chen, Maohua; Wu, Da; Wang, Youchun; Bi, Shengli; Qiu, Yan; Lu, Peng; Cheng, Jing; Xiao, Bai; Hu, Liangping; Gao, Xing; Liu, Jingzhong; Wang, Yiping; Song, Yingzhao; Zhang, Liqun; Suo, Fengshuang; Chen, Tongyan; Huang, Zeyu; Zhao, Yunzhuan; Lu, Hong; Pan, Chunqin; Tang, Hong title: Proteomic Fingerprints for Potential Application to Early Diagnosis of Severe Acute Respiratory Syndrome date: 2005-01-01 journal: Clin Chem DOI: 10.1373/clinchem.2004.032458 sha: doc_id: 273035 cord_uid: sewfb3q8 file: cache/cord-351498-bmq6zcb0.json key: cord-351498-bmq6zcb0 authors: Martínez-Sernández, Victoria; Perteguer, María J.; Hernández-González, Ana; Mezo, Mercedes; González-Warleta, Marta; Orbegozo-Medina, Ricardo A.; Romarís, Fernanda; Paniagua, Esperanza; Gárate, Teresa; Ubeira, Florencio M. title: Comparison of recombinant cathepsins L1, L2, and L5 as ELISA targets for serodiagnosis of bovine and ovine fascioliasis date: 2018-03-21 journal: Parasitol Res DOI: 10.1007/s00436-018-5809-7 sha: doc_id: 351498 cord_uid: bmq6zcb0 file: cache/cord-265740-wjdeps3h.json key: cord-265740-wjdeps3h authors: Radbel, Jared; Jagpal, Sugeet; Roy, Jason; Brooks, Andrew; Tischfield, Jay; Sheldon, Michael; Bixby, Christian; Witt, Dana; Gennaro, Maria Laura; Horton, Daniel B.; Barrett, Emily S.; Carson, Jeffrey L.; Panettieri, Reynold A.; Blaser, Martin J. title: Detection of SARS-CoV-2 is comparable in clinical samples preserved in saline or viral transport media date: 2020-05-13 journal: J Mol Diagn DOI: 10.1016/j.jmoldx.2020.04.209 sha: doc_id: 265740 cord_uid: wjdeps3h file: cache/cord-275779-ocbygkyb.json key: cord-275779-ocbygkyb authors: Ye, Zi-Wei; Yuan, Shuofeng; Poon, Kwok-Man; Wen, Lei; Yang, Dong; Sun, Zehua; Li, Cun; Hu, Meng; Shuai, Huiping; Zhou, Jie; Zhang, Mei-Yun; Zheng, Bo-Jian; Chu, Hin; Yuen, Kwok-Yung title: Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice date: 2017-03-21 journal: Front Immunol DOI: 10.3389/fimmu.2017.00317 sha: doc_id: 275779 cord_uid: ocbygkyb file: cache/cord-305648-majanu8l.json key: cord-305648-majanu8l authors: Schountz, Tony; Calisher, Charles H.; Richens, Tiffany R.; Rich, Audrey A.; Doty, Jeffrey B.; Hughes, Mark T.; Beaty, Barry J. title: Rapid Field Immunoassay for Detecting Antibody to Sin Nombre Virus in Deer Mice date: 2007-10-17 journal: Emerg Infect Dis DOI: 10.3201/eid1310.070383 sha: doc_id: 305648 cord_uid: majanu8l file: cache/cord-292862-ezrkg0dc.json key: cord-292862-ezrkg0dc authors: Myerson, Jacob W.; Patel, Priyal N.; Habibi, Nahal; Walsh, Landis R.; Lee, Yi-Wei; Luther, David C.; Ferguson, Laura T.; Zaleski, Michael H.; Zamora, Marco E.; Marcos-Contreras, Oscar A.; Glassman, Patrick M.; Johnston, Ian; Hood, Elizabeth D.; Shuvaeva, Tea; Gregory, Jason V.; Kiseleva, Raisa Y.; Nong, Jia; Rubey, Kathryn M.; Greineder, Colin F.; Mitragotri, Samir; Worthen, George S.; Rotello, Vincent M.; Lahann, Joerg; Muzykantov, Vladimir R.; Brenner, Jacob S. title: Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment date: 2020-04-18 journal: bioRxiv DOI: 10.1101/2020.04.15.037564 sha: doc_id: 292862 cord_uid: ezrkg0dc file: cache/cord-347661-q9lgliph.json key: cord-347661-q9lgliph authors: Zevenhoven-Dobbe, Jessika C.; Wassenaar, Alfred L. M.; van der Meer, Yvonne; Snijder, Eric J. title: Production of Monospecific Rabbit Antisera Recognizing Nidovirus Proteins date: 2007-11-28 journal: SARS- and Other Coronaviruses DOI: 10.1007/978-1-59745-181-9_16 sha: doc_id: 347661 cord_uid: q9lgliph file: cache/cord-339694-sp212tai.json key: cord-339694-sp212tai authors: Jiang, Xinpeng; Hou, Xingyu; Tang, Lijie; Jiang, Yanping; Ma, Guangpeng; Li, Yijing title: A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection date: 2016-03-28 journal: Appl Microbiol Biotechnol DOI: 10.1007/s00253-016-7424-9 sha: doc_id: 339694 cord_uid: sp212tai file: cache/cord-332221-6ea6gz9s.json key: cord-332221-6ea6gz9s authors: Li, Guiping; Zhou, Lijuan; Zhang, Can; Shi, Yun; Dong, Derong; Bai, Miao; Wang, Rong; Zhang, Chuanfu title: Insulin-Like Growth Factor 1 Regulates Acute Inflammatory Lung Injury Mediated by Influenza Virus Infection date: 2019-11-26 journal: Front Microbiol DOI: 10.3389/fmicb.2019.02541 sha: doc_id: 332221 cord_uid: 6ea6gz9s file: cache/cord-334165-7gfk554m.json key: cord-334165-7gfk554m authors: Stadlbauer, Daniel; Amanat, Fatima; Chromikova, Veronika; Jiang, Kaijun; Strohmeier, Shirin; Arunkumar, Guha Asthagiri; Tan, Jessica; Bhavsar, Disha; Capuano, Christina; Kirkpatrick, Ericka; Meade, Philip; Brito, Ruhi Nichalle; Teo, Catherine; McMahon, Meagan; Simon, Viviana; Krammer, Florian title: SARS‐CoV‐2 Seroconversion in Humans: A Detailed Protocol for a Serological Assay, Antigen Production, and Test Setup date: 2020-04-17 journal: Curr Protoc Microbiol DOI: 10.1002/cpmc.100 sha: doc_id: 334165 cord_uid: 7gfk554m file: cache/cord-340125-il35gs97.json key: cord-340125-il35gs97 authors: Jayapal, Manikandan; Tay, Hwee Kee; Reghunathan, Renji; Zhi, Liang; Chow, Kah Kiong; Rauff, Mary; Melendez, Alirio J title: Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses date: 2006-08-16 journal: BMC Genomics DOI: 10.1186/1471-2164-7-210 sha: doc_id: 340125 cord_uid: il35gs97 file: cache/cord-298224-flyx85lr.json key: cord-298224-flyx85lr authors: Hibbitts, Alan J.; Ramsey, Joanne M.; Barlow, James; MacLoughlin, Ronan; Cryan, Sally-Ann title: In Vitro and In Vivo Assessment of PEGylated PEI for Anti-IL-8/CxCL-1 siRNA Delivery to the Lungs date: 2020-06-27 journal: Nanomaterials (Basel) DOI: 10.3390/nano10071248 sha: doc_id: 298224 cord_uid: flyx85lr file: cache/cord-327568-5vo4nmei.json key: cord-327568-5vo4nmei authors: Tosini, Fabio; Ludovisi, Alessandra; Tonanzi, Daniele; Amati, Marco; Cherchi, Simona; Pozio, Edoardo; Gómez-Morales, Maria Angeles title: Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection date: 2019-05-15 journal: Parasit Vectors DOI: 10.1186/s13071-019-3486-8 sha: doc_id: 327568 cord_uid: 5vo4nmei file: cache/cord-295033-5fd9bu60.json key: cord-295033-5fd9bu60 authors: Parma, Y.R.; Chacana, P.A.; Rogé, A.; Kahl, A.; Cangelosi, A.; Geoghegan, P.; Lucchesi, P.M.A.; Fernández-Miyakawa, M.E. title: Antibodies anti-Shiga toxin 2 B subunit from chicken egg yolk: Isolation, purification and neutralization efficacy date: 2011-09-15 journal: Toxicon DOI: 10.1016/j.toxicon.2011.07.009 sha: doc_id: 295033 cord_uid: 5fd9bu60 file: cache/cord-356207-tpn5cg4n.json key: cord-356207-tpn5cg4n authors: Beniac, Daniel R; Andonov, Anton; Grudeski, Elsie; Booth, Tim F title: Architecture of the SARS coronavirus prefusion spike date: 2006-07-16 journal: Nat Struct Mol Biol DOI: 10.1038/nsmb1123 sha: doc_id: 356207 cord_uid: tpn5cg4n file: cache/cord-343409-oao75pzy.json key: cord-343409-oao75pzy authors: Hayward, Joshua A; Tachedjian, Mary; Cui, Jie; Field, Hume; Holmes, Edward C; Wang, Lin-Fa; Tachedjian, Gilda title: Identification of diverse full-length endogenous betaretroviruses in megabats and microbats date: 2013-03-27 journal: Retrovirology DOI: 10.1186/1742-4690-10-35 sha: doc_id: 343409 cord_uid: oao75pzy file: cache/cord-333639-usgpe1cz.json key: cord-333639-usgpe1cz authors: Zuwala, Kaja; Riber, Camilla F.; Løvschall, Kaja Borup; Andersen, Anna H.F.; Sørensen, Lise; Gajda, Paulina; Tolstrup, Martin; Zelikin, Alexander N. title: Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects date: 2018-04-10 journal: J Control Release DOI: 10.1016/j.jconrel.2018.02.012 sha: doc_id: 333639 cord_uid: usgpe1cz file: cache/cord-335121-ro3x3qa3.json key: cord-335121-ro3x3qa3 authors: Ingram, George A.; Al-Yaman, Fadwa title: A comparative assessment of four serological methods used in the detection and measurement of anti-parasite antibodies in the serum of the amphibian, bufo viridis date: 1988-04-30 journal: International Journal for Parasitology DOI: 10.1016/0020-7519(88)90147-6 sha: doc_id: 335121 cord_uid: ro3x3qa3 file: cache/cord-335591-r0x8yaqj.json key: cord-335591-r0x8yaqj authors: Ohnishi, Kazuo title: Establishment and Characterization of Monoclonal Antibodies Against SARS Coronavirus date: 2007-11-28 journal: SARS- and Other Coronaviruses DOI: 10.1007/978-1-59745-181-9_15 sha: doc_id: 335591 cord_uid: r0x8yaqj Reading metadata file and updating bibliogrpahics === updating bibliographic database Building study carrel named keyword-pbs-cord === file2bib.sh === id: cord-305648-majanu8l author: Schountz, Tony title: Rapid Field Immunoassay for Detecting Antibody to Sin Nombre Virus in Deer Mice date: 2007-10-17 pages: extension: .txt txt: ./txt/cord-305648-majanu8l.txt cache: ./cache/cord-305648-majanu8l.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-305648-majanu8l.txt' === file2bib.sh === id: cord-259094-5qzbctan author: Xu, Mei Ling title: The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection date: 2013-04-26 pages: extension: .txt txt: ./txt/cord-259094-5qzbctan.txt cache: ./cache/cord-259094-5qzbctan.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-259094-5qzbctan.txt' === file2bib.sh === id: cord-356207-tpn5cg4n author: Beniac, Daniel R title: Architecture of the SARS coronavirus prefusion spike date: 2006-07-16 pages: extension: .txt txt: ./txt/cord-356207-tpn5cg4n.txt cache: ./cache/cord-356207-tpn5cg4n.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 2 resourceName b'cord-356207-tpn5cg4n.txt' === file2bib.sh === id: cord-303381-xvzhb7ix author: TSURUTA, Yuya title: The requirement of environmental acidification for Ibaraki virus infection to host cells date: 2015-08-28 pages: extension: .txt txt: ./txt/cord-303381-xvzhb7ix.txt cache: ./cache/cord-303381-xvzhb7ix.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-303381-xvzhb7ix.txt' === file2bib.sh === id: cord-265740-wjdeps3h author: Radbel, Jared title: Detection of SARS-CoV-2 is comparable in clinical samples preserved in saline or viral transport media date: 2020-05-13 pages: extension: .txt txt: ./txt/cord-265740-wjdeps3h.txt cache: ./cache/cord-265740-wjdeps3h.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-265740-wjdeps3h.txt' === file2bib.sh === id: cord-267736-rya9w6sh author: Kang, Xiaoping title: Development of an ELISA-array for simultaneous detection of five encephalitis viruses date: 2012-02-27 pages: extension: .txt txt: ./txt/cord-267736-rya9w6sh.txt cache: ./cache/cord-267736-rya9w6sh.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 2 resourceName b'cord-267736-rya9w6sh.txt' === file2bib.sh === id: cord-335121-ro3x3qa3 author: Ingram, George A. title: A comparative assessment of four serological methods used in the detection and measurement of anti-parasite antibodies in the serum of the amphibian, bufo viridis date: 1988-04-30 pages: extension: .txt txt: ./txt/cord-335121-ro3x3qa3.txt cache: ./cache/cord-335121-ro3x3qa3.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-335121-ro3x3qa3.txt' === file2bib.sh === id: cord-002583-cgcf7mgj author: Zhuo, Xun-hui title: Evaluation of potential anti-toxoplasmosis efficiency of combined traditional herbs in a mouse model date: 2017-06-01 pages: extension: .txt txt: ./txt/cord-002583-cgcf7mgj.txt cache: ./cache/cord-002583-cgcf7mgj.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-002583-cgcf7mgj.txt' === file2bib.sh === id: cord-335591-r0x8yaqj author: Ohnishi, Kazuo title: Establishment and Characterization of Monoclonal Antibodies Against SARS Coronavirus date: 2007-11-28 pages: extension: .txt txt: ./txt/cord-335591-r0x8yaqj.txt cache: ./cache/cord-335591-r0x8yaqj.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-335591-r0x8yaqj.txt' === file2bib.sh === id: cord-009800-tajkpgkj author: Orellana, Mhica V. title: An immunoprobe to measure Rubisco concentrations and maximal photosynthetic rates of individual phytoplankton cells date: 2003-12-22 pages: extension: .txt txt: ./txt/cord-009800-tajkpgkj.txt cache: ./cache/cord-009800-tajkpgkj.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 2 resourceName b'cord-009800-tajkpgkj.txt' === file2bib.sh === id: cord-275635-d50bxe7c author: Yuan, Xiaomin title: Efficacy and immunogenicity of recombinant swinepox virus expressing the A epitope of the TGEV S protein date: 2015-07-31 pages: extension: .txt txt: ./txt/cord-275635-d50bxe7c.txt cache: ./cache/cord-275635-d50bxe7c.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-275635-d50bxe7c.txt' === file2bib.sh === id: cord-338108-3rn6fwx3 author: Jin, Yi title: Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection date: 2013-09-18 pages: extension: .txt txt: ./txt/cord-338108-3rn6fwx3.txt cache: ./cache/cord-338108-3rn6fwx3.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-338108-3rn6fwx3.txt' === file2bib.sh === id: cord-013265-qrfi6e5c author: Isono, Toshihito title: Treatment of severe pneumonia by hinokitiol in a murine antimicrobial-resistant pneumococcal pneumonia model date: 2020-10-15 pages: extension: .txt txt: ./txt/cord-013265-qrfi6e5c.txt cache: ./cache/cord-013265-qrfi6e5c.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-013265-qrfi6e5c.txt' === file2bib.sh === id: cord-335310-61wibso4 author: Chen, Hui-Wen title: Synthetic virus-like particles prepared via protein corona formation enable effective vaccination in an avian model of coronavirus infection date: 2016-08-15 pages: extension: .txt txt: ./txt/cord-335310-61wibso4.txt cache: ./cache/cord-335310-61wibso4.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-335310-61wibso4.txt' === file2bib.sh === id: cord-278802-bverdk5w author: Zhou, Yefei title: Immune response of AA broilers to IBV H120 vaccine and sodium new houttuyfonate date: 2010-12-31 pages: extension: .txt txt: ./txt/cord-278802-bverdk5w.txt cache: ./cache/cord-278802-bverdk5w.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-278802-bverdk5w.txt' === file2bib.sh === id: cord-274396-l611eisi author: Park, Su-Jin title: Antiviral Efficacies of FDA-Approved Drugs against SARS-CoV-2 Infection in Ferrets date: 2020-05-22 pages: extension: .txt txt: ./txt/cord-274396-l611eisi.txt cache: ./cache/cord-274396-l611eisi.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-274396-l611eisi.txt' === file2bib.sh === id: cord-259364-8zoav7b0 author: Xiao, Yire title: Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis date: 2019-09-09 pages: extension: .txt txt: ./txt/cord-259364-8zoav7b0.txt cache: ./cache/cord-259364-8zoav7b0.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-259364-8zoav7b0.txt' === file2bib.sh === id: cord-273035-sewfb3q8 author: Kang, Xixiong title: Proteomic Fingerprints for Potential Application to Early Diagnosis of Severe Acute Respiratory Syndrome date: 2005-01-01 pages: extension: .txt txt: ./txt/cord-273035-sewfb3q8.txt cache: ./cache/cord-273035-sewfb3q8.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-273035-sewfb3q8.txt' === file2bib.sh === id: cord-275779-ocbygkyb author: Ye, Zi-Wei title: Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice date: 2017-03-21 pages: extension: .txt txt: ./txt/cord-275779-ocbygkyb.txt cache: ./cache/cord-275779-ocbygkyb.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-275779-ocbygkyb.txt' === file2bib.sh === id: cord-002013-rb9xdzro author: Zheng, Xuexing title: Treatment with hyperimmune equine immunoglobulin or immunoglobulin fragments completely protects rodents from Ebola virus infection date: 2016-04-12 pages: extension: .txt txt: ./txt/cord-002013-rb9xdzro.txt cache: ./cache/cord-002013-rb9xdzro.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-002013-rb9xdzro.txt' === file2bib.sh === id: cord-276732-u2d1z4ip author: Mauri, Tommaso title: Intraperitoneal adoptive transfer of mesenchymal stem cells enhances recovery from acid aspiration acute lung injury in mice date: 2017-03-06 pages: extension: .txt txt: ./txt/cord-276732-u2d1z4ip.txt cache: ./cache/cord-276732-u2d1z4ip.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-276732-u2d1z4ip.txt' === file2bib.sh === id: cord-011106-h20vbmbo author: Takeda, Yohei title: Antiviral Activities of Hibiscus sabdariffa L. Tea Extract Against Human Influenza A Virus Rely Largely on Acidic pH but Partially on a Low-pH-Independent Mechanism date: 2019-10-16 pages: extension: .txt txt: ./txt/cord-011106-h20vbmbo.txt cache: ./cache/cord-011106-h20vbmbo.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-011106-h20vbmbo.txt' === file2bib.sh === id: cord-334165-7gfk554m author: Stadlbauer, Daniel title: SARS‐CoV‐2 Seroconversion in Humans: A Detailed Protocol for a Serological Assay, Antigen Production, and Test Setup date: 2020-04-17 pages: extension: .txt txt: ./txt/cord-334165-7gfk554m.txt cache: ./cache/cord-334165-7gfk554m.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-334165-7gfk554m.txt' === file2bib.sh === id: cord-001065-j4hvyyoi author: Boncristiani, Humberto F. title: In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) date: 2013-09-05 pages: extension: .txt txt: ./txt/cord-001065-j4hvyyoi.txt cache: ./cache/cord-001065-j4hvyyoi.txt Content-Encoding ISO-8859-1 Content-Type text/plain; charset=ISO-8859-1 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-001065-j4hvyyoi.txt' === file2bib.sh === id: cord-001732-4eyn7pjq author: Riede, O title: Preclinical safety and tolerability of a repeatedly administered human leishmaniasis DNA vaccine date: 2015-04-30 pages: extension: .txt txt: ./txt/cord-001732-4eyn7pjq.txt cache: ./cache/cord-001732-4eyn7pjq.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-001732-4eyn7pjq.txt' === file2bib.sh === id: cord-339694-sp212tai author: Jiang, Xinpeng title: A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection date: 2016-03-28 pages: extension: .txt txt: ./txt/cord-339694-sp212tai.txt cache: ./cache/cord-339694-sp212tai.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-339694-sp212tai.txt' === file2bib.sh === id: cord-295033-5fd9bu60 author: Parma, Y.R. title: Antibodies anti-Shiga toxin 2 B subunit from chicken egg yolk: Isolation, purification and neutralization efficacy date: 2011-09-15 pages: extension: .txt txt: ./txt/cord-295033-5fd9bu60.txt cache: ./cache/cord-295033-5fd9bu60.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-295033-5fd9bu60.txt' === file2bib.sh === id: cord-309742-fd1qmr87 author: Slepushkin, Vladimir A. title: Infection of Human Airway Epithelia with H1N1, H2N2, and H3N2 Influenza A Virus Strains date: 2016-12-14 pages: extension: .txt txt: ./txt/cord-309742-fd1qmr87.txt cache: ./cache/cord-309742-fd1qmr87.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-309742-fd1qmr87.txt' === file2bib.sh === id: cord-001017-4qfhltg4 author: Chatterjee, Dhriti title: Microglia Play a Major Role in Direct Viral-Induced Demyelination date: 2013-06-20 pages: extension: .txt txt: ./txt/cord-001017-4qfhltg4.txt cache: ./cache/cord-001017-4qfhltg4.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 2 resourceName b'cord-001017-4qfhltg4.txt' === file2bib.sh === id: cord-264267-weat0qs6 author: Kleine-Weber, Hannah title: Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus date: 2020-01-21 pages: extension: .txt txt: ./txt/cord-264267-weat0qs6.txt cache: ./cache/cord-264267-weat0qs6.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-264267-weat0qs6.txt' === file2bib.sh === id: cord-013526-6fip93l2 author: Labadie, Thomas title: A non-enveloped arbovirus released in lysosome-derived extracellular vesicles induces super-infection exclusion date: 2020-10-19 pages: extension: .txt txt: ./txt/cord-013526-6fip93l2.txt cache: ./cache/cord-013526-6fip93l2.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-013526-6fip93l2.txt' === file2bib.sh === id: cord-332221-6ea6gz9s author: Li, Guiping title: Insulin-Like Growth Factor 1 Regulates Acute Inflammatory Lung Injury Mediated by Influenza Virus Infection date: 2019-11-26 pages: extension: .txt txt: ./txt/cord-332221-6ea6gz9s.txt cache: ./cache/cord-332221-6ea6gz9s.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 2 resourceName b'cord-332221-6ea6gz9s.txt' === file2bib.sh === id: cord-277054-eq4obbte author: Kaur, Manpreet title: Rabies DNA vaccine: No impact of MHC Class I and Class II targeting sequences on immune response and protection against lethal challenge date: 2009-03-26 pages: extension: .txt txt: ./txt/cord-277054-eq4obbte.txt cache: ./cache/cord-277054-eq4obbte.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-277054-eq4obbte.txt' === file2bib.sh === id: cord-347661-q9lgliph author: Zevenhoven-Dobbe, Jessika C. title: Production of Monospecific Rabbit Antisera Recognizing Nidovirus Proteins date: 2007-11-28 pages: extension: .txt txt: ./txt/cord-347661-q9lgliph.txt cache: ./cache/cord-347661-q9lgliph.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-347661-q9lgliph.txt' === file2bib.sh === id: cord-327568-5vo4nmei author: Tosini, Fabio title: Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection date: 2019-05-15 pages: extension: .txt txt: ./txt/cord-327568-5vo4nmei.txt cache: ./cache/cord-327568-5vo4nmei.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-327568-5vo4nmei.txt' === file2bib.sh === id: cord-260834-v254de8k author: Lim, Chia Chiu title: Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies date: 2019-04-15 pages: extension: .txt txt: ./txt/cord-260834-v254de8k.txt cache: ./cache/cord-260834-v254de8k.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-260834-v254de8k.txt' === file2bib.sh === id: cord-026866-0hlre9i6 author: Perruzza, Lisa title: Prophylactic Activity of Orally Administered FliD-Reactive Monoclonal SIgA Against Campylobacter Infection date: 2020-06-09 pages: extension: .txt txt: ./txt/cord-026866-0hlre9i6.txt cache: ./cache/cord-026866-0hlre9i6.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-026866-0hlre9i6.txt' === file2bib.sh === id: cord-340125-il35gs97 author: Jayapal, Manikandan title: Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses date: 2006-08-16 pages: extension: .txt txt: ./txt/cord-340125-il35gs97.txt cache: ./cache/cord-340125-il35gs97.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-340125-il35gs97.txt' === file2bib.sh === id: cord-333639-usgpe1cz author: Zuwala, Kaja title: Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects date: 2018-04-10 pages: extension: .txt txt: ./txt/cord-333639-usgpe1cz.txt cache: ./cache/cord-333639-usgpe1cz.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-333639-usgpe1cz.txt' === file2bib.sh === id: cord-308461-4lhh3du0 author: Ueki, Hiroshi title: Multicolor two-photon imaging of in vivo cellular pathophysiology upon influenza virus infection using the two-photon IMPRESS date: 2020-01-29 pages: extension: .txt txt: ./txt/cord-308461-4lhh3du0.txt cache: ./cache/cord-308461-4lhh3du0.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-308461-4lhh3du0.txt' === file2bib.sh === id: cord-003915-kje8lvgl author: Pigeyre, Laetitia title: Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda date: 2019-09-17 pages: extension: .txt txt: ./txt/cord-003915-kje8lvgl.txt cache: ./cache/cord-003915-kje8lvgl.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-003915-kje8lvgl.txt' === file2bib.sh === id: cord-351498-bmq6zcb0 author: Martínez-Sernández, Victoria title: Comparison of recombinant cathepsins L1, L2, and L5 as ELISA targets for serodiagnosis of bovine and ovine fascioliasis date: 2018-03-21 pages: extension: .txt txt: ./txt/cord-351498-bmq6zcb0.txt cache: ./cache/cord-351498-bmq6zcb0.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-351498-bmq6zcb0.txt' === file2bib.sh === id: cord-000354-05lnj3w0 author: de Vries, Erik title: Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway date: 2011-03-31 pages: extension: .txt txt: ./txt/cord-000354-05lnj3w0.txt cache: ./cache/cord-000354-05lnj3w0.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-000354-05lnj3w0.txt' === file2bib.sh === id: cord-295416-y3lvcjqd author: Eichinger, Katherine M. title: Prefusion RSV F Immunization Elicits Th2-Mediated Lung Pathology in Mice When Formulated With a Th2 (but Not a Th1/Th2-Balanced) Adjuvant Despite Complete Viral Protection date: 2020-07-29 pages: extension: .txt txt: ./txt/cord-295416-y3lvcjqd.txt cache: ./cache/cord-295416-y3lvcjqd.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-295416-y3lvcjqd.txt' === file2bib.sh === id: cord-298224-flyx85lr author: Hibbitts, Alan J. title: In Vitro and In Vivo Assessment of PEGylated PEI for Anti-IL-8/CxCL-1 siRNA Delivery to the Lungs date: 2020-06-27 pages: extension: .txt txt: ./txt/cord-298224-flyx85lr.txt cache: ./cache/cord-298224-flyx85lr.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 3 resourceName b'cord-298224-flyx85lr.txt' === file2bib.sh === id: cord-343409-oao75pzy author: Hayward, Joshua A title: Identification of diverse full-length endogenous betaretroviruses in megabats and microbats date: 2013-03-27 pages: extension: .txt txt: ./txt/cord-343409-oao75pzy.txt cache: ./cache/cord-343409-oao75pzy.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-343409-oao75pzy.txt' === file2bib.sh === id: cord-292862-ezrkg0dc author: Myerson, Jacob W. title: Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment date: 2020-04-18 pages: extension: .txt txt: ./txt/cord-292862-ezrkg0dc.txt cache: ./cache/cord-292862-ezrkg0dc.txt Content-Encoding UTF-8 Content-Type text/plain; charset=UTF-8 X-Parsed-By ['org.apache.tika.parser.DefaultParser', 'org.apache.tika.parser.csv.TextAndCSVParser'] X-TIKA:content_handler ToTextContentHandler X-TIKA:embedded_depth 0 X-TIKA:parse_time_millis 4 resourceName b'cord-292862-ezrkg0dc.txt' Que is empty; done keyword-pbs-cord === reduce.pl bib === id = cord-002013-rb9xdzro author = Zheng, Xuexing title = Treatment with hyperimmune equine immunoglobulin or immunoglobulin fragments completely protects rodents from Ebola virus infection date = 2016-04-12 pages = extension = .txt mime = text/plain words = 6027 sentences = 286 flesch = 56 summary = To investigate whether EBOV infections can be controlled by virus neutralization alone, and to prevent the possible induction of serum sickness in humans that would be administered antisera, the post-exposure efficacy of F(ab′ ) 2 (immunoglobulin treated with pepsin to remove the Fc regions of the antibody) were also investigated side-by-side with equine antisera in all experiments as a potential alternate treatment. Three horses were immunized intramuscularly (IM) with 7 injections of eVLP over 11 weeks and the hyperimmune sera were collected from each animal at specified timepoints ( Fig. 1A) to determine the serum titers by neutralization assay against a recombinant HIV-1 virus pseudotyped with EBOV GP. The observation that administering F(ab′ ) 2 at 1 dpi is more efficacious than when the same treatment was given at 30 minutes post-exposure (Fig. 5A ) was also observed in past studies with therapeutic EBOV GP-specific monoclonal antibodies 25, 26 , and suggests that virus neutralization may play a bigger role in protection at a later timepoint after EBOV challenge. cache = ./cache/cord-002013-rb9xdzro.txt txt = ./txt/cord-002013-rb9xdzro.txt === reduce.pl bib === id = cord-003915-kje8lvgl author = Pigeyre, Laetitia title = Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda date = 2019-09-17 pages = extension = .txt mime = text/plain words = 9040 sentences = 462 flesch = 47 summary = As orally transmitted viruses, densoviruses, are also challenged by the complexity of the insect gut barriers, more specifically by the chitinous peritrophic matrix, that lines and protects the midgut epithelium; how capsids stick to and cross these barriers to reach their final cell destination where replication goes has been poorly studied in insects. In addition, we showed that JcDV early infection results in (i) an arrest of N-Acetylglucosamine (GlcNAc) secretion by epithelial cells associated with a disorganization of the PM structure mimicking the effect of chitin-binding plant lectin; (ii) substantial changes in the expression of gut genes, which may also contribute to an early gut dysfunction and participate to viral pathogenesis. Results presented here show that JcDV capsids display carbohydrate-binding properties that insure recognition of the peritrophic matrix and determines caterpillars oral infection. cache = ./cache/cord-003915-kje8lvgl.txt txt = ./txt/cord-003915-kje8lvgl.txt === reduce.pl bib === id = cord-001732-4eyn7pjq author = Riede, O title = Preclinical safety and tolerability of a repeatedly administered human leishmaniasis DNA vaccine date = 2015-04-30 pages = extension = .txt mime = text/plain words = 6339 sentences = 336 flesch = 49 summary = Evaluation of single-dose and repeated-dose toxicity of the vaccine candidate after i.d. administration to naive, non-infected mice did not reveal any safety concerns. To assess toxicity of LEISHDNAVAX in naive mice, sterile phosphate-buffered saline (PBS, placebo) and ascending doses of the vaccine were injected either once or five times in weekly intervals (Table 1) . Twenty-four hour after single or repeated injection, MIDGE-Th1 vector DNA was detected in almost all organs and tissues examined, suggesting that it was distributed systemically, most likely via the lymphatic system and the blood stream. Groups of 10 BALB/c mice (5 male, 5 female) were immunized i.d. at the tail base five times in weekly intervals with either PBS or LEISHDNAVAX (10, 50 or 100 μg per dose). In summary, we have shown here that LEISHDNAVAX, a novel DNA vaccine candidate against leishmaniasis is safe and well tolerated in both naive and Leishmania-infected mice. cache = ./cache/cord-001732-4eyn7pjq.txt txt = ./txt/cord-001732-4eyn7pjq.txt === reduce.pl bib === id = cord-001017-4qfhltg4 author = Chatterjee, Dhriti title = Microglia Play a Major Role in Direct Viral-Induced Demyelination date = 2013-06-20 pages = extension = .txt mime = text/plain words = 6654 sentences = 312 flesch = 42 summary = Previous studies demonstrated that microglia can be persistently infected by neurotropic mouse hepatitis virus (MHV) which causes meningoencephalitis, myelitis with subsequent axonal loss, and demyelination and serve as a virus-induced model of human neurological disease multiple sclerosis (MS). In our current studies, we have used RSA59 infection in vivo, in vitro, and ex vivo as a model to understand whether MHV can directly infect CNS resident microglia and the mechanism of microglial activation in the induction of chronic demyelination. To confirm the RSA59-induced CNS inflammation, brain and spinal cord sections from day 7 (peak of inflammation) and day 30 (peak of demyelination) postinfected mice were stained with H&E or LFB and examined. While Iba1 immunofluorescence was observed in both gray and white matter, double fluorescence/immunofluorescence demonstrated dual labelling of EGFP (viral antigen) positive Iba1 positive microglia/macrophages were present only in the white matter of RSA59 infected mice (Figure 1 ). cache = ./cache/cord-001017-4qfhltg4.txt txt = ./txt/cord-001017-4qfhltg4.txt === reduce.pl bib === id = cord-011106-h20vbmbo author = Takeda, Yohei title = Antiviral Activities of Hibiscus sabdariffa L. Tea Extract Against Human Influenza A Virus Rely Largely on Acidic pH but Partially on a Low-pH-Independent Mechanism date = 2019-10-16 pages = extension = .txt mime = text/plain words = 5362 sentences = 330 flesch = 54 summary = Here, we analyzed the antiviral activity of hibiscus (Hibiscus sabdariffa L.) tea extract against human IAV and evaluated its potential as a novel anti-IAV drug and a safe inactivating agent for whole inactivated vaccine. In addition, we assessed hibiscus tea extract's potential as a candidate for novel anti-IAV drug and as an inactivating agent for whole-virus vaccines. PR8 virus propagated in allantoic fluid was mixed with an equal amount of neutral and acidic pH PBS, Hib[crude], frHibis, or PCA. 50 μl PBS, formalin-, β-PL-, or acidic Hib[crude]-inactivated PR8 virus vaccine was intranasally administered in mice (first vaccination) under light anesthesia with isolflurane (Intervet K.K., Tokyo, Japan). The neutralized Hib[crude] in the blood loses potent anti-IAV activity due to acid, and the low-pH-independent antiviral activity is inadequate to inactivate virus in vivo. cache = ./cache/cord-011106-h20vbmbo.txt txt = ./txt/cord-011106-h20vbmbo.txt === reduce.pl bib === id = cord-013526-6fip93l2 author = Labadie, Thomas title = A non-enveloped arbovirus released in lysosome-derived extracellular vesicles induces super-infection exclusion date = 2020-10-19 pages = extension = .txt mime = text/plain words = 8084 sentences = 379 flesch = 51 summary = Here we used Bluetongue virus (BTV) as a model of a non-enveloped arthropod-borne virus and discovered that the majority of viruses are released in EVs. Based on the cellular proteins detected in these EVs, and use of inhibitors targeting the cellular degradation process, we demonstrated that these extracellular vesicles are derived from secretory lysosomes, in which the acidic pH is neutralized upon the infection. Virus released in secretory lysosomes infectious EVs. However, inhibition of autophagosome-lysosome fusion with chloroquine (CQ), led to a significant reduction of infectious EVs released as compared to the control ( Fig 2B) , indicating that the late steps of autophagy are necessary for infectious EVs. In addition, inhibition of MVBs regulator protein HSP90 using geldanamycin in BTV-infected cells (MOI = 10) also led to a significant reduction of infectivity measured in the EVs fraction, as compared to the control, indicating a possible role for MVBs in the release of infectious EVs. In contrast, GW4869, a drug that inhibits the release of exosomes (small vesicles~200nm) derived from MVBs, did not affect the secretion levels of EVs containing BTV ( Fig 2B) . cache = ./cache/cord-013526-6fip93l2.txt txt = ./txt/cord-013526-6fip93l2.txt === reduce.pl bib === id = cord-009800-tajkpgkj author = Orellana, Mhica V. title = An immunoprobe to measure Rubisco concentrations and maximal photosynthetic rates of individual phytoplankton cells date = 2003-12-22 pages = extension = .txt mime = text/plain words = 5874 sentences = 306 flesch = 42 summary = The cross‐reactivity of an immunological probe to the key photosynthetic enzyme Rubisco (ribulose‐1,5‐bisphosphate carboxylase/oxygenase) was characterized as part of a larger effort to determine maximal photosynthetic rates of individual phytoplankton cells. In order to use an immunoprobe to quantitatively measure Rubisco concentration within individual cells in a mixed-species assemblage, it is imperative to determine: first, whether the probe is truly specific to only the large subunit of Rubisco; second, whether the probe binds to the Rubisco large subunit of all phytoplankton species with equal affinity; and third, whether immunologically determined concentrations of Rubisco are well correlated with maximal photosynthetic rates. The results indicate that an affinity-purified anti-Rubisco probe can be used to quantify Rubisco concentrations and maximal photosynthetic potential of individual phytoplankton cells in mixed-species assemblages. When the more quantitative dot blot assays were used with purified Rubisco from different species, a high degree of variability in the binding affinity with the polyclonal antiserum was evident (Fig. 1) . cache = ./cache/cord-009800-tajkpgkj.txt txt = ./txt/cord-009800-tajkpgkj.txt === reduce.pl bib === id = cord-001065-j4hvyyoi author = Boncristiani, Humberto F. title = In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) date = 2013-09-05 pages = extension = .txt mime = text/plain words = 6367 sentences = 326 flesch = 47 summary = title: In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) An experimental protocol to test these systems was developed, using injections of Israeli Acute Paralysis Virus (IAPV) into honey bee pupae reared ex-situ under laboratory conditions. Gene expression analyses of three separate experiments suggest IAPV disruption of transcriptional homeostasis of several fundamental cellular functions, including an up-regulation of the ribosomal biogenesis pathway. Little is known about the specific biology of the viruses in these families that infect honey bees, although they contain important bee pathogens, such as Deformed Wing Virus (DWV) and Israeli Acute Paralysis Virus (IAPV). Post-hoc tests of main treatment effects showed significantly higher gene expression in the IAPV-inoculated bees compared to the two control groups for Actin, 28S rRNA, and mGST1. The observed gene expression patterns could be due to viral manipulation of the cells to increase virus replication or present cell compensatory responses to IAPV infection. cache = ./cache/cord-001065-j4hvyyoi.txt txt = ./txt/cord-001065-j4hvyyoi.txt === reduce.pl bib === id = cord-267736-rya9w6sh author = Kang, Xiaoping title = Development of an ELISA-array for simultaneous detection of five encephalitis viruses date = 2012-02-27 pages = extension = .txt mime = text/plain words = 2990 sentences = 178 flesch = 47 summary = The ELISA-array assay is based on a "sandwich" ELISA format and consists of viral antibodies printed directly on 96-well microtiter plates, allowing for direct detection of 5 viruses. The developed ELISA-array proved to have similar specificity and higher sensitivity compared with the conventional ELISAs. This method was validated by different viral cultures and three chicken eggs inoculated with infected patient serum. The results demonstrated that this method combined the advantage of ELISA and protein array (multiplex and ease of use) and has potential for the identification of clinical encephalitis virus. When spotting, different spotting buffers and concentrations of capture monoclonal antibodies were evaluated to optimize the ELISA-array assay. To verify the results tested by ELISA-array, RNA extracted from chicken eggs was applied to a real time-RT-PCR assay using primers and probes targeting TBEV. In this study, we developed a multiplex ELISA-based method in a double-antibody sandwich format for the simultaneous detection of five encephalitis-associated viral pathogens. cache = ./cache/cord-267736-rya9w6sh.txt txt = ./txt/cord-267736-rya9w6sh.txt === reduce.pl bib === id = cord-000354-05lnj3w0 author = de Vries, Erik title = Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway date = 2011-03-31 pages = extension = .txt mime = text/plain words = 10971 sentences = 561 flesch = 48 summary = The sensitivity of the dynamin-independent entry pathway to inhibitors or dominant-negative mutants affecting actomyosin dynamics as well as to a number of specific inhibitors of growth factor receptor tyrosine kinases and downstream effectors thereof all point to the involvement of macropinocytosis in IAV entry. As factors present in serum are known for their potential to induce specific endocytic pathways, we further explored the conditions required for the novel DYNA-IND IAV entry pathway (using the Gluc-entry assay) by inoculating cells in PBS in the presence of increasing concentrations of fetal calf serum (FCS). Growth factor inducible activation of the tyrosine kinase src has also been linked to the induction of macropinocytosis [49] [50] [51] ; consistent with this observation the src inhibitor PP2 [52] specifically inhibited DYNA-IND entry of IAV (Fig. 9A-B) . cache = ./cache/cord-000354-05lnj3w0.txt txt = ./txt/cord-000354-05lnj3w0.txt === reduce.pl bib === id = cord-013265-qrfi6e5c author = Isono, Toshihito title = Treatment of severe pneumonia by hinokitiol in a murine antimicrobial-resistant pneumococcal pneumonia model date = 2020-10-15 pages = extension = .txt mime = text/plain words = 4585 sentences = 252 flesch = 38 summary = To evaluate the efficacy of repeated hinokitiol administration in a pneumonia mouse model, all mice were intratracheally infected with S. Here, compared with PBS injection, intratracheal administration of 500 μg/mL hinokitiol in a pneumococcal pneumonia mouse model decreased inflammatory cell migration and prevented destruction of alveolar tissue (Fig 2) . However, in clinical settings, antimicrobial agents are administrated several times for the treatment of pneumococcal pneumonia, and thus, we next sought to investigate whether repeated hinokitiol injection decreased the bacterial load in (Fig 7; P < 0.05) . The present study showed that intratracheal administration of hinokitiol decreased the bacterial load in a mouse pneumonia model regardless of macrolide resistance of S. In this study, intratracheal hinokitiol administration reduced neutrophil infiltration and elastase release in the lungs of pneumonia mice, consequently diminishing lung injury and pneumococcal DNA detection in serum. cache = ./cache/cord-013265-qrfi6e5c.txt txt = ./txt/cord-013265-qrfi6e5c.txt === reduce.pl bib === id = cord-002583-cgcf7mgj author = Zhuo, Xun-hui title = Evaluation of potential anti-toxoplasmosis efficiency of combined traditional herbs in a mouse model date = 2017-06-01 pages = extension = .txt mime = text/plain words = 3785 sentences = 197 flesch = 57 summary = The results showed that the survival time of mice in the 500 mg Chinese herbs group and sulfadiazine group was significantly longer than that of the PBS control group. Also the parasite load in blood and tissues of 500 mg Chinese herbs and sulfadiazine groups was significantly lower than that of PBS group at 7 days post infection (dpi), which was in accordance with the result of histological detection. Results of spleen, lung, and liver tissues presented a similar pattern in that parasite loads were all largely increased from 3 to 7 dpi, and mice of the PBS control group had statistically significantly higher parasite load compared with sulfadiazine and 500 mg Chinese herb groups (P<0.05). The lungs of sulfadiazine and Chinese herbs-treated mice possessed a significantly lower parasite load than that of the PBS control group (P<0.05) and the histological result verified this from the morphological perspective. cache = ./cache/cord-002583-cgcf7mgj.txt txt = ./txt/cord-002583-cgcf7mgj.txt === reduce.pl bib === id = cord-275635-d50bxe7c author = Yuan, Xiaomin title = Efficacy and immunogenicity of recombinant swinepox virus expressing the A epitope of the TGEV S protein date = 2015-07-31 pages = extension = .txt mime = text/plain words = 3979 sentences = 212 flesch = 54 summary = To explore the possibility of developing a vaccine against transmissible gastroenteritis virus (TGEV) infection, a recombinant swinepox virus (rSPV-SA) expressing a TGEV protective antigen has been constructed. Results from the passive immunity protection test of new born piglets demonstrated that the recombinant live-vector vaccine, rSPV-SA, could 100% protect piglets from the SPV infection, and there was no significant clinical symptom in the rSPV-SA treatment group during this experiment. Eight one-month-old swine (Large White) were randomly divided into four groups (2 pigs per group) and were immunized twice at 0 and 28 days with infectious rSPV-SA (1 × 10 8 PFU/ml in 2 ml of PBS), inactivated-TGEV (1 × 10 8 PFU/ml in 2 ml of PBS), wtSPV (1 × 10 8 PFU/ml in 2 ml of PBS) or PBS, each time via three routes: oral, nasal, and intraperitoneal. To explore whether mice or swine generated TGEV neutralizing antibodies, serum from the PBS, wtSPV, inactivated-TGEV and rSPV-SA treated mice and pig were collected at 0, 14, 21, 35, 42 days post-primary immunization (1:100-1:12,800 dilution in a 100 l volume). cache = ./cache/cord-275635-d50bxe7c.txt txt = ./txt/cord-275635-d50bxe7c.txt === reduce.pl bib === id = cord-026866-0hlre9i6 author = Perruzza, Lisa title = Prophylactic Activity of Orally Administered FliD-Reactive Monoclonal SIgA Against Campylobacter Infection date = 2020-06-09 pages = extension = .txt mime = text/plain words = 9357 sentences = 371 flesch = 38 summary = In this study, we describe the prophylactic activity of orally delivered recombinant SIgA generated from two human monoclonal antibodies (CAA1 and CCG4) isolated for their reactivity against the flagellar-capping protein FliD, which is essential for bacteria motility and highly conserved across Campylobacter species associated with severe enteritis. In this study, we describe the prophylactic activity of orally delivered recombinant SIgA generated from two human monoclonal antibodies (CAA1 and CCG4) isolated for their reactivity against the flagellar-capping protein FliD, which is essential for bacteria motility and highly conserved across Campylobacter species associated with severe enteritis. In this study, an immunocompetent mouse model of Campylobacter infection was used to evaluated the prophylactic activity of orally delivered recombinant SIgA generated from human monoclonal antibodies isolated and selected for their reactivity against the flagellar-capping protein FliD, which is pivotal for bacteria motility (25), and highly conserved across Campylobacter species frequently associated with severe neonatal enteritis (26) . cache = ./cache/cord-026866-0hlre9i6.txt txt = ./txt/cord-026866-0hlre9i6.txt === reduce.pl bib === id = cord-259094-5qzbctan author = Xu, Mei Ling title = The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection date = 2013-04-26 pages = extension = .txt mime = text/plain words = 2514 sentences = 142 flesch = 54 summary = title: The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection In this study, we isolated the acidic protein fraction of bovine colostrum (AFC, isoelectric point <5) by anion-exchange chromatography, and investigated the effect of its dietary intake on influenza A (H1N1) virus infection. In this study we isolated the acidic protein fraction of bovine colostrum (AFC) and investigated how dietary intake of AFC modulates the symptoms of influenza infection. The three mouse groups were given oseltamivir, PBS and AFC orally for 14 days prior to infection with influenza A virus. Therefore, the effect of total bovine colostrums on influenza virus infection in mice was significantly different from our expectation. In this study, we provide the first evidence that orally supplemented AFC is effective in reducing the symptoms associated with influenza A virus infection. cache = ./cache/cord-259094-5qzbctan.txt txt = ./txt/cord-259094-5qzbctan.txt === reduce.pl bib === id = cord-259364-8zoav7b0 author = Xiao, Yire title = Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis date = 2019-09-09 pages = extension = .txt mime = text/plain words = 4494 sentences = 247 flesch = 56 summary = title: Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis The aim of this study was to estimate the therapeutic potential of specific egg yolk immunoglobulin (IgY) on dermatophytosis caused by Trichophyton rubrum. rubrum cell wall proteins IgY (anti-trCWP IgY) presented a certain degree of cross-reactivity with different fungi. In the in vitro and in vivo activity researches, Anti-trCWP IgY showed a significant dose-dependent growth inhibitory effect on T. To estimate the cross-reactivity (CR) of anti-trCWP IgY against other fungi, indirect ELISAs were performed by the use of antigens from different fungi according to the method described previously. rubrum and the protective effect of anti-trCWP IgY against dermatophytosis of experimentally infected mice. In our study, the cell wall proteins showed good immunogenicity, highest titer of anti-trCWP IgY reaching 1:16000. rubrum in a dose-dependent manner compared with IgY from unimmunized hens,and significantly reduced lesion scores of mice experimentally infected with T. cache = ./cache/cord-259364-8zoav7b0.txt txt = ./txt/cord-259364-8zoav7b0.txt === reduce.pl bib === id = cord-264267-weat0qs6 author = Kleine-Weber, Hannah title = Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus date = 2020-01-21 pages = extension = .txt mime = text/plain words = 7200 sentences = 325 flesch = 47 summary = Four polymorphisms (K267E, K267N, A291P and Δ346-348) strongly reduced binding of MERS-CoV S to DPP4 and S protein-driven host cell entry, as determined using soluble S protein and S protein bearing rhabdoviral vectors, respectively. For host cell entry, the surface unit, S1, of MERS-CoV S binds to the cellular type-II transmembrane protein dipeptidyl peptidase 4 (DPP4, CD26) [15] . For the binding studies with solMERS-S1-Fc, a similar protocol was followed as described for the analysis of DPP4 surface expression with the exceptions that sol-MERS-S1-Fc was used instead of the primary antibody (1:10 dilution in PBS/BSA) and that an AlexaFluor488conjugated anti-human antibody (goat, 1:500 dilution in PBS/BSA, ThermoFisher Scientific) was employed as the secondary antibody. Reduced MERS-CoV S-driven host cell entry is caused by inefficient S protein binding to DPP4 harboring polymorphic amino acid residues. cache = ./cache/cord-264267-weat0qs6.txt txt = ./txt/cord-264267-weat0qs6.txt === reduce.pl bib === id = cord-295416-y3lvcjqd author = Eichinger, Katherine M. title = Prefusion RSV F Immunization Elicits Th2-Mediated Lung Pathology in Mice When Formulated With a Th2 (but Not a Th1/Th2-Balanced) Adjuvant Despite Complete Viral Protection date = 2020-07-29 pages = extension = .txt mime = text/plain words = 9392 sentences = 452 flesch = 46 summary = These data suggest that in the absence of preimmunity, stabilized PreF antigens may still be associated with aberrant Th2 responses that induce lung pathology in response to RSV infection, and can be prevented by formulation with more Th1/Th2-balanced adjuvants that enhance CD4+ and CD8+ IFNγ+ T cell responses. The objective of this study was to determine the capacity of RSV pre-fusion (PreF) vaccines formulated with different adjuvants to generate neutralizing antibody, prevent virus replication, and protect from pulmonary pathology following RSV challenge. Despite lower neutralizing antibody titers in mice immunized with PreF/Advax-SM, as compared to PreF/Alum, both immunization groups had undetectable RSV in their lungs at 4 dpi ( Figure 1F ). Taken together, these data indicate that RSV PreF immunization formulated with Th1-skewing adjuvants, like Advax-SM, provide protection against RSV infection in naïve BALB/c mice as compared to alum by inhibiting viral replication without eliciting enhanced pulmonary pathology. cache = ./cache/cord-295416-y3lvcjqd.txt txt = ./txt/cord-295416-y3lvcjqd.txt === reduce.pl bib === id = cord-338108-3rn6fwx3 author = Jin, Yi title = Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection date = 2013-09-18 pages = extension = .txt mime = text/plain words = 3969 sentences = 242 flesch = 50 summary = title: Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection In this study, we evaluated the immunomodulatory activities and protective effect of Eupatorium adenophorum polysaccharide (EAP) against the highly pathogenic H5N1 subtype influenza virus. EAP treatment significantly increased the production of IL-6, TNF-α, and IFN-γ both in vivo and in vitro as measured by qPCR and ELISA. In a mouse infection model, intranasal administration of EAP at a dose of 25 mg/kg body weight prior to H5N1 viral challenge efficiently inhibited viral replication, decreased lung lesions, and increased survival rate. To detect IL-6, TNF-, and IFN-expression, lungs of five mice per group were collected at day 0 before infection and tested by qPCR and ELISA. In this study, we evaluated the immunomodulatory activities and protective effect of EAP against H5N1 influenza infection in a mouse model. cache = ./cache/cord-338108-3rn6fwx3.txt txt = ./txt/cord-338108-3rn6fwx3.txt === reduce.pl bib === id = cord-274396-l611eisi author = Park, Su-Jin title = Antiviral Efficacies of FDA-Approved Drugs against SARS-CoV-2 Infection in Ferrets date = 2020-05-22 pages = extension = .txt mime = text/plain words = 4355 sentences = 208 flesch = 46 summary = While the lopinavir-ritonavir-, hydroxychloroquine sulfate-, or emtricitabine-tenofovir-treated group exhibited lower overall clinical scores than the phosphate-buffered saline (PBS)-treated control group, the virus titers in nasal washes, stool specimens, and respiratory tissues were similar between all three antiviral-candidate-treated groups and the PBS-treated control group. Compared to the PBS-treated control group, azathioprine-immunosuppressed ferrets exhibited a longer period of clinical illness, higher virus titers in nasal turbinate, delayed virus clearance, and significantly lower serum neutralization (SN) antibody titers. In order to determine the antiviral efficacies of lopinavir-ritonavir, hydroxychloroquine (HCQ) sulfate, or emtricitabine-tenofovir for treatment of SARS-CoV-2 infection, SARS-CoV-2 antibody-free ferrets (10/group) were inoculated with 10 5.8 50% tissue culture infective doses (TCID 50 )/ml of an NMC-nCoV02 strain through the intranasal (i.n.) route ( Fig. 1 ). Therefore, although clinical symptoms were attenuated in ferret groups treated with antiviral candidates, we also evaluated virus titers in respiratory and gastrointestinal tracts using nasal washes and stool samples, respectively, from SARS-CoV-2-infected ferrets. cache = ./cache/cord-274396-l611eisi.txt txt = ./txt/cord-274396-l611eisi.txt === reduce.pl bib === id = cord-308461-4lhh3du0 author = Ueki, Hiroshi title = Multicolor two-photon imaging of in vivo cellular pathophysiology upon influenza virus infection using the two-photon IMPRESS date = 2020-01-29 pages = extension = .txt mime = text/plain words = 8337 sentences = 517 flesch = 47 summary = Unlike ex vivo methods, which involve isolated or sliced lungs, in vivo imaging using two-photon excitation microscopy of live animals enables researchers to observe hemodynamics, migration and extravasation of immune cells, as well as interactions among immune cells during influenza virus infection. To detect multiple fluorescent signals excited simultaneously by a two-photon excitation laser, fluorochromes with different spectra and equal brightness must be selected; however, there is currently no comprehensive database of fluorescent reagents, fluorescent reporter viruses, and reporter mouse lines available for lung in vivo imaging. Our system uses suction-based lung stabilization 16, 28 to improve an existing in vivo two-photon imaging system for influenza virus-infected lung as a model of an acute inflammatory respiratory disease 5 . In vivo two-photon imaging is performed under conditions of single stimulation with a two-photon excitation laser; limitations exist regarding available fluorescent reagents/proteins for multiple labeling of target cells and lung architecture. cache = ./cache/cord-308461-4lhh3du0.txt txt = ./txt/cord-308461-4lhh3du0.txt === reduce.pl bib === id = cord-335310-61wibso4 author = Chen, Hui-Wen title = Synthetic virus-like particles prepared via protein corona formation enable effective vaccination in an avian model of coronavirus infection date = 2016-08-15 pages = extension = .txt mime = text/plain words = 5482 sentences = 264 flesch = 40 summary = Herein, a facile approach to formulate synthetic virus-like particles (sVLPs) is demonstrated by exploiting the phenomenon of protein corona formation induced by the high-energy surfaces of synthetic nanoparticles. As compared to inoculation with free proteins, vaccination with the sVLPs showed enhanced lymphatic antigen delivery, stronger antibody titers, increased splenic T-cell response, and reduced infection-associated symptoms in an avian model of coronavirus infection. Comparison to a commercial whole inactivated virus vaccine also showed evidence of superior antiviral protection by the sVLPs. The study demonstrates a simple yet robust method in bridging viral antigens with synthetic nanoparticles for improved vaccine application; it has practical implications in the management of human viral infections as well as in animal agriculture. In the present study, vaccination with the sVLPs resulted in enhanced humoral and cellular immune responses, improving protection against an avian model of coronavirus infection as compared to free protein antigens and a commercial WIV vaccine. cache = ./cache/cord-335310-61wibso4.txt txt = ./txt/cord-335310-61wibso4.txt === reduce.pl bib === id = cord-309742-fd1qmr87 author = Slepushkin, Vladimir A. title = Infection of Human Airway Epithelia with H1N1, H2N2, and H3N2 Influenza A Virus Strains date = 2016-12-14 pages = extension = .txt mime = text/plain words = 5526 sentences = 311 flesch = 48 summary = Therefore, we assayed A/PR/8/34 (H1N1), A/Japan/305/57 (H2N2), and X31 (H3N2) influenza virus strains for binding and infection on fully differentiated primary cultures of airway epithelia isolated from human bronchus, grown on semiporous filters at an air–liquid interface. These data show that influenza viruses with SAα2,3Gal binding specificity, like Japan, productively infect differentiated human airway epithelia from the apical surface. For measurement of the kinetics of influenza virus production from infected airway cells in one infectious cycle, 100 l of the virus preparation was diluted in Dulbecco's PBS (Life Technologies, Inc., Grand Island, NY) and applied to the apical surface of the epithelia (m.o.i. of 0.1). To infect airway epithelia with different influenza virus strains from the basolateral side, the Millicell culture insert was turned over and virus preparations diluted in PBS were applied in a 100-l volume to the bottom of the membrane (m.o.i. ϭ 0.1). cache = ./cache/cord-309742-fd1qmr87.txt txt = ./txt/cord-309742-fd1qmr87.txt === reduce.pl bib === id = cord-303381-xvzhb7ix author = TSURUTA, Yuya title = The requirement of environmental acidification for Ibaraki virus infection to host cells date = 2015-08-28 pages = extension = .txt mime = text/plain words = 1987 sentences = 121 flesch = 49 summary = The effect of environmental acidification on Ibaraki virus (IBAV) infection was tested using endosomal inhibitory chemicals and low pH treatment. Treatment of target cells with endosomal inhibitors significantly decreased the progeny virus production. HmLu-1 (hamster lung) cells were infected with IBAV in the presence of three different endosome inhibitors, bafilomycin A1 (Baf A1, Sigma, St. Louis, MO, U.S.A.), chlorpromazine (CPZ, Abcam, Cambridge, U.K.) and dynasore (Wako, Osaka, Japan). These results indicated that IBAV utilizes clathrin-dependent endosomal pathway for infection and coincided with the previous research on bluetongue virus entry [8] . To confirm the effect of low pH on virus infectivity, purified IBAV was incubated in PBS (−) with several pH (pH=4, 7 or 9) for five min and infected to HmLu-1 at MOI=0.01. The result obtained above implicated that low pH treat-ment removes IBAV outer capsid proteins from the particle and initiates its infection. cache = ./cache/cord-303381-xvzhb7ix.txt txt = ./txt/cord-303381-xvzhb7ix.txt === reduce.pl bib === id = cord-278802-bverdk5w author = Zhou, Yefei title = Immune response of AA broilers to IBV H120 vaccine and sodium new houttuyfonate date = 2010-12-31 pages = extension = .txt mime = text/plain words = 3161 sentences = 177 flesch = 57 summary = On 0, 7, 14, 21, 28 and 35 post first vaccination, the dynamic changes of peripheral lymphocyte proliferation, cytokine assays and serum antibody titers were assayed respectively by MTT method, ELISA and hemagglutination inhibition assay (HI). The results showed that sodium new houttuyfonate significantly raised IB antibody titer in the chickens and also markedly promoted lymphocyte proliferation. Five chickens were sampled randomly from each group for assay of lymphocyte proliferation by MTT method and 10 chickens from each group for assessment of serum HI antibody titer by the micro-method and cytokines by ELISA kits at 0, 7, 14, 21 and 35 days post the primary immunization (dpi). In this study, with chicken IBV H120 strain live attenuated vaccine in chickens, by measuring peripheral blood lymphocyte proliferation and serum cytokines and antibody titers, the humoral and cellular immunity induced with SNH was researched. cache = ./cache/cord-278802-bverdk5w.txt txt = ./txt/cord-278802-bverdk5w.txt === reduce.pl bib === id = cord-276732-u2d1z4ip author = Mauri, Tommaso title = Intraperitoneal adoptive transfer of mesenchymal stem cells enhances recovery from acid aspiration acute lung injury in mice date = 2017-03-06 pages = extension = .txt mime = text/plain words = 4445 sentences = 210 flesch = 47 summary = -Arterial blood gas analysis for gas exchange -Wet-to-dry ratio as index of edema -Micro-CT scan to measure change over time in non-aerated lung tissue expressed as percentage of the whole lung tissue, with more negative values representing larger decrease of alveolar collapse; -Histopathology examination performed according to previous study [12] evaluating alveolar serofibrinous exudate and alveolar hemorrhage -Bronchoalveolar lavage for differential cell count, total protein content (with bicinchoninic acid method) and keratinocyte chemoattractant (CXCL1, previously named KC), and tumor necrosis factor-α (TNF-α) were assayed by ELISA -Blood withdrawal for PTX3 levels measurement in plasma (ELISA assay) (b)In 1 week from lung injury D-dimer (marker of fibrinolysis) [20] and matrix metalloproteinase 13 (MMP13), an enzyme that participates in collagen degradation [21] , were detected by ELISA and by western blot in lungs lysate, respectively. cache = ./cache/cord-276732-u2d1z4ip.txt txt = ./txt/cord-276732-u2d1z4ip.txt === reduce.pl bib === id = cord-260834-v254de8k author = Lim, Chia Chiu title = Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies date = 2019-04-15 pages = extension = .txt mime = text/plain words = 8295 sentences = 456 flesch = 52 summary = The phage ELISA was conducted to measure the performances and effects of different blocking agents on the binding of αUbi phages against crude rUbi. Out of the four samples, the combination of PTM buffer and lysate showed the highest signal (1.226) detected with anti-c-myc-HRP as shown in Fig. 4c . Lysate preblocking and phage preincubation effects towards αUbi and M13KO7 phages against rUbi. To further optimize the biopanning conditions against crude antigens, the 'Yin-Yang' (capture and eliminate) approach was designed to reduce non-specific binding by background phages. coli proteins in the crude fraction of rUbi with the actual concentration of rUbi being expected to be lower than the purified rUbi, the binding capability of αUbi is still unaffected as shown in phage ELISA assay upon affinity selection against crude rUbi. The blocking effect of PTM and E. cache = ./cache/cord-260834-v254de8k.txt txt = ./txt/cord-260834-v254de8k.txt === reduce.pl bib === id = cord-273035-sewfb3q8 author = Kang, Xixiong title = Proteomic Fingerprints for Potential Application to Early Diagnosis of Severe Acute Respiratory Syndrome date = 2005-01-01 pages = extension = .txt mime = text/plain words = 4128 sentences = 177 flesch = 50 summary = Background: Definitive early-stage diagnosis of severe acute respiratory syndrome (SARS) is important despite the number of laboratory tests that have been developed to complement clinical features and epidemiologic data in case definition. Results: The discriminatory classifier with a panel of four biomarkers determined in the training set could precisely detect 36 of 37 (sensitivity, 97.3%) acute SARS and 987 of 993 (specificity, 99.4%) non-SARS samples. We established a decision tree algorithm consisting of four unique biomarkers for acute SARS in the training set and subsequently validated the accuracy of this classifier by use of a completely blinded test set. To identify the serum biomarkers that could distinguish SARS from non-SARS samples, we used a training set of specimens (37 SARS acute and 74 controls; Tables 1 and 2) and constructed the decision tree classification algorithm using 10 989 peaks [99 peaks ϫ (37 ϩ 74) spectra] of statistical significance identified in the low energy readings (see Materials and Methods). cache = ./cache/cord-273035-sewfb3q8.txt txt = ./txt/cord-273035-sewfb3q8.txt === reduce.pl bib === id = cord-277054-eq4obbte author = Kaur, Manpreet title = Rabies DNA vaccine: No impact of MHC Class I and Class II targeting sequences on immune response and protection against lethal challenge date = 2009-03-26 pages = extension = .txt mime = text/plain words = 6906 sentences = 378 flesch = 45 summary = The potency of modified DNA vaccines assessed by total antibody response, antibody isotypes, cytokine profile, neutralizing antibody titer and protection conferred against in vivo challenge; was enhanced in comparison to native unmodified vaccine, but the response elicited did not pertain to the type of target sequence and the directed arm of immunity. The ability of these DNA vaccines to elicit protective responses in immunized mice was assessed by intracerebral challenge with 20 LD 50 of virulent rabies virus CVS strain. In an effort to develop an optimal DNA vaccine against rabies virus, this study was aimed at evaluating the immune enhancement potential of different antigen targeting strategies to selectively improve responses mediated by CD8 + and CD4 + T lymphocytes and by antibodies, induced after intramuscular immunization with DNA plasmids. also reported that DNA vaccine encoding rabies virus glycoprotein lacking transmembrane domain though enhances antibody response but does not confer protection [35] . cache = ./cache/cord-277054-eq4obbte.txt txt = ./txt/cord-277054-eq4obbte.txt === reduce.pl bib === id = cord-351498-bmq6zcb0 author = Martínez-Sernández, Victoria title = Comparison of recombinant cathepsins L1, L2, and L5 as ELISA targets for serodiagnosis of bovine and ovine fascioliasis date = 2018-03-21 pages = extension = .txt mime = text/plain words = 8277 sentences = 401 flesch = 48 summary = In the present study, we developed and tested three indirect ELISAs using rFhpCL1, rFhpCL2, and rFhpCL5 and evaluated their recognition by sera from sheep and cattle naturally infected with F. In the present study, we developed and tested indirect ELISAs based on recombinant procathepsin L1 (rFhpCL1), rFhpCL2, or rFhpCL5, in order to investigate which of these targets are best recognized by sera from sheep and cattle naturally infected with F. Finally, the r values obtained on comparing the four ELISA methods for Fasciola-infected cattle and sheep sera are shown in Table 3 . These results suggest that the use of a single recombinant cathepsin/ procathepsin as target antigen in ELISAs for serodiagnosis of fascioliasis may limit the sensitivity of the assay when testing sera from some species, particularly cattle. (2001) who tested sera from sheep and cattle harboring other parasites, mainly nematodes, suggesting that the cross-reactivity may be due to common epitopes between recombinant Fasciola cathepsins and antigens present in other parasites. cache = ./cache/cord-351498-bmq6zcb0.txt txt = ./txt/cord-351498-bmq6zcb0.txt === reduce.pl bib === id = cord-265740-wjdeps3h author = Radbel, Jared title = Detection of SARS-CoV-2 is comparable in clinical samples preserved in saline or viral transport media date = 2020-05-13 pages = extension = .txt mime = text/plain words = 2250 sentences = 121 flesch = 51 summary = Given that SARS-CoV-2 viral RNA has demonstrated stability, we posited that phosphate buffered saline (PBS) may be a viable transport medium, as an alternative to VTM), for clinical qPCR testing. We assessed the intraand inter-individual reliability of SARS-CoV-2 qPCR in clinical endotracheal secretion samples transported in VTM or PBS, evaluating the stability of the RT-qPCR signal for three viral targets (N gene, ORF1ab, and S gene) when samples were stored in these media at room temperature for up to 18 hours. We report that using PBS as a transport medium has high intra-and inter-individual reliability, maintains viral stability, and is comparable to VTM in the detection of the three SARS-CoV-2 genes through 18 hours of storage. SARS-CoV-2 detection using standard testing of upper airway secretions requires a nasopharyngeal (NP) or oropharyngeal (OP) swab that is transported to a clinical laboratory using viral transport media (VTM) (https://www.fda.gov/medical-devices/emergency-situations-medical-devices/faqs-diagnostic-testingsars-cov-2#offeringtests, last accessed April 29 2020). cache = ./cache/cord-265740-wjdeps3h.txt txt = ./txt/cord-265740-wjdeps3h.txt === reduce.pl bib === id = cord-275779-ocbygkyb author = Ye, Zi-Wei title = Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice date = 2017-03-21 pages = extension = .txt mime = text/plain words = 5425 sentences = 253 flesch = 42 summary = title: Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice Engaging the antibody-dependent cell-mediated cytotoxicity (ADCC) for killing of virus-infected cells and secretion of antiviral cytokines and chemokines was incorporated as one of the important features in the design of universal influenza vaccines. In this study, we determined the ADCC and antiviral activities of two putative ADCC epitopes, designated E1 and E2, on the HA head of a pandemic H1N1 influenza virus in vitro and in a lethal mouse model. The phenotype was potentially due to an exaggerated inflammatory cell infiltration triggered by ADCC, as an upregulated release of cytotoxic granules (perforin) was observed in the lung tissue of E1-vaccinated mice after H1N1 influenza virus challenge. While the antiviral efficacy provided by the stalk-specific ADCC antibodies has been confirmed (12) , our data raised concerns on the side effect of certain HA head epitopes in devising a universal influenza vaccine. cache = ./cache/cord-275779-ocbygkyb.txt txt = ./txt/cord-275779-ocbygkyb.txt === reduce.pl bib === id = cord-347661-q9lgliph author = Zevenhoven-Dobbe, Jessika C. title = Production of Monospecific Rabbit Antisera Recognizing Nidovirus Proteins date = 2007-11-28 pages = extension = .txt mime = text/plain words = 6866 sentences = 343 flesch = 53 summary = The use as antigens of either synthetic peptides (coupled to a carrier protein) or proteins expressed in Escherichia coli is described, and detailed protocols for immunization and preparation of test bleeds are provided. Furthermore, in the context of specific research questions, polyclonal antisera may sometimes even be preferred over monoclonal antibodies since they contain a mixture of immunoglobulin molecules, derived from different B-cell lines in the immunized animal, often recognizing multiple epitopes of the target protein. The antiserum used here was raised against a domain in the C-terminal region of pp1a of the arterivirus EAV (8) and recognizes a large set of processing intermediates and end products, which are indicated by arrowheads: (A) Western blot analysis: EAV-and mock-infected cell lysates were prepared at 8 h postinfection, run on an SDS-polyacrylamide gel, blotted to PVDF membrane, and incubated with the postimmune serum at a 1:1000 dilution. cache = ./cache/cord-347661-q9lgliph.txt txt = ./txt/cord-347661-q9lgliph.txt === reduce.pl bib === id = cord-305648-majanu8l author = Schountz, Tony title = Rapid Field Immunoassay for Detecting Antibody to Sin Nombre Virus in Deer Mice date = 2007-10-17 pages = extension = .txt mime = text/plain words = 1633 sentences = 96 flesch = 57 summary = We developed a 1-hour field enzyme immunoassay (EIA) for detecting antibody to Sin Nombre virus in deer mice (Peromyscus maniculatus). Samples were retested under laboratory conditions with PAGEIA and standard Centers for Disease Control and Prevention (CDC) enzyme immunoassay (EIA) (5) . One sample (HA-2564) was scored negative by fi eld and laboratory PAGEIA, but (low) positive (optical density [OD] of 0.327) by conventional EIA (Table) . One sample (TS-0830-7) scored as 1+ in the fi eld was determined to be negative on subsequent laboratory testing by both PAGEIA and conventional EIA. The other 4 samples (HB-2628, HA-2609, HA-2616, HB-2710) were scored as positive by fi eld and laboratory PAGEIA but negative by conventional EIA. Similar laboratorybased PAGEIAs have also been used to detect antibody to antigens of agents causing other infectious diseases, including severe acute respiratory syndrome coronavirus-like viruses and Nipah virus in bats (13) (14) (15) . cache = ./cache/cord-305648-majanu8l.txt txt = ./txt/cord-305648-majanu8l.txt === reduce.pl bib === id = cord-339694-sp212tai author = Jiang, Xinpeng title = A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection date = 2016-03-28 pages = extension = .txt mime = text/plain words = 6818 sentences = 358 flesch = 44 summary = title: A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection casei) vaccine against anti-transmissible gastroenteritis virus developed in our laboratory was used to study mucosal immune responses. We found that the recombinant Lactobacillus stimulated IL-17 expression in both the systemic and mucosal immune responses against TGEV infection. Following infection with virulent transmissible gastroenteritis coronavirus, isolated mesenteric lymph node CD4+ T cells mounted a specific proliferative response against infectious or inactivated purified virus upon secondary in vitro stimulation (Anton et al. Here, an oral Lactobacillus casei vaccine against anti-transmissible gastroenteritis virus developed in our laboratory was used to study the mucosal immune response (Jiang et al. In conclusion, our study suggests that the recombinant Lactobacillus vaccine provokes specific mucosal and systemic immune responses to protect piglets from infection. cache = ./cache/cord-339694-sp212tai.txt txt = ./txt/cord-339694-sp212tai.txt === reduce.pl bib === id = cord-292862-ezrkg0dc author = Myerson, Jacob W. title = Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment date = 2020-04-18 pages = extension = .txt mime = text/plain words = 14275 sentences = 744 flesch = 46 summary = We show that polystyrene nanoparticles and five liposome formulations do not accumulate in injured lungs, indicating that nanostructures that are not based on protein are not intrinsically drawn to marginated neutrophils in acute inflammation. 6, 10, 14, 18 Single cell suspensions prepared from mouse lungs were probed by flow cytometry to further characterize pulmonary neutrophils in naïve mice and in mice following LPS-induced inflammation. The protein component of each particle was labeled with 125 I for tracing in biodistributions, and assessed 30 minutes after IV administration of NPs. Both absolute LDNG lung uptake and ratio of lung uptake to liver uptake registered a ~25-fold increase between naïve control and LPS-injured animals (Figure 2A , Supplementary Table 1) . As with LDNGs and albumin NPs in Figure 2C -H, single cell suspensions were prepared from LPS-inflamed and naïve control lungs after circulation of fluorescent DBCO-IgG liposomes. cache = ./cache/cord-292862-ezrkg0dc.txt txt = ./txt/cord-292862-ezrkg0dc.txt === reduce.pl bib === id = cord-332221-6ea6gz9s author = Li, Guiping title = Insulin-Like Growth Factor 1 Regulates Acute Inflammatory Lung Injury Mediated by Influenza Virus Infection date = 2019-11-26 pages = extension = .txt mime = text/plain words = 6779 sentences = 332 flesch = 50 summary = The expression of inflammatory cytokines in the serum was detected by enzyme linked immunosorbent assay; lung injury was observed by hematoxylin-eosin staining; the viral proliferation in the lung was detected by real-time quantitative PCR; and the protein expression of the main molecules in the phosphatidylinositol-3-kinases/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signaling pathways was detected by Western blot. The expression of inflammatory cytokines in the serum was detected by enzyme linked immunosorbent assay; lung injury was observed by hematoxylin-eosin staining; the viral proliferation in the lung was detected by real-time quantitative PCR; and the protein expression of the main molecules in the phosphatidylinositol-3-kinases/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signaling pathways was detected by Western blot. To explore the mechanism by which IGF1 regulates acute inflammatory lung injury induced by IAV infection, a Western blot was used to detect the expression of molecules in key signaling pathways in the lung tissue of PR8-infected mice (50LD 50 PR8). cache = ./cache/cord-332221-6ea6gz9s.txt txt = ./txt/cord-332221-6ea6gz9s.txt === reduce.pl bib === id = cord-334165-7gfk554m author = Stadlbauer, Daniel title = SARS‐CoV‐2 Seroconversion in Humans: A Detailed Protocol for a Serological Assay, Antigen Production, and Test Setup date = 2020-04-17 pages = extension = .txt mime = text/plain words = 5286 sentences = 414 flesch = 69 summary = Basic Protocol 1: Mammalian cell transfection and protein purification Basic Protocol 2: A two‐stage ELISA for high‐throughput screening of human serum samples for antibodies binding to the spike protein of SARS‐CoV‐2 We reported in our earlier work that individuals not exposed to SARS-CoV-2 are completely naïve to the spike protein, and their serum samples show little or no reactivity in an ELISA (Amanat et al., 2020) . We developed this as a two-stage ELISA in which the first stage ('a' steps below) includes relatively high-throughput screening of samples in a single serum dilution against the RBD (which expresses very well and therefore can be produced in greater quantities). This is followed by a second stage ('b' steps below) in which positive samples from the first stage undergo a confirmatory ELISA against the full-length spike protein (which is harder to express; therefore there is usually less available). i. Thaw the required number of vials of antigen (SARS-CoV-2 RBD protein) to coat 96-well microtiter ELISA plates at a concentration of 2 μg/ml. cache = ./cache/cord-334165-7gfk554m.txt txt = ./txt/cord-334165-7gfk554m.txt === reduce.pl bib === id = cord-340125-il35gs97 author = Jayapal, Manikandan title = Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses date = 2006-08-16 pages = extension = .txt mime = text/plain words = 7377 sentences = 380 flesch = 48 summary = title: Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses A substantial number of genes were regulated by IgE sensitization alone; and following FcεRI aggregation, a wide range of genes were triggered, including genes for cytokines, chemokines, transcription factors, anti-apoptosis, and several genes involved in innate and acquired immunity. Other than these, several genes coding for other receptors involved in immune-responses; immunoregulatory genes; adhesion and/or cytoskeleton remodeling; regulators of apoptosis; signal transduction; transcription factors; were also upregulated by monomeric IgE (Table. Here we studied, whether monomeric-IgE alone, may activate FcεRI intracellular signaling pathways, leading to physiological responses of mast cells, by analyzing the overall tyrosine phosphorylation; fluctuations in cytosolic Ca 2+ concentration; and degranulation by measuring β-hexosaminidase release (Fig. 6A,B &6C) . cache = ./cache/cord-340125-il35gs97.txt txt = ./txt/cord-340125-il35gs97.txt === reduce.pl bib === id = cord-298224-flyx85lr author = Hibbitts, Alan J. title = In Vitro and In Vivo Assessment of PEGylated PEI for Anti-IL-8/CxCL-1 siRNA Delivery to the Lungs date = 2020-06-27 pages = extension = .txt mime = text/plain words = 11340 sentences = 633 flesch = 56 summary = Following optimization with antiglyceraldehyde 3-phosphate dehydrogenase (GAPDH) siRNA, PEI and PEI-LPEG anti-IL8 siRNA nanoparticles were assessed for efficacy using polarised Calu-3 human airway epithelial cells and a twin stage impinger (TSI) in vitro lung model. This work demonstrates the potential of nebulised PEI-PEG siRNA nanoparticles in modulating pulmonary inflammation and highlights the need to move towards more relevant in vitro and in vivo models for respiratory drug development. In contrast, the nebulised PEI-LPEG siRNA nanoparticles demonstrated significantly greater levels of GAPDH knockdown versus the PBS-treated controls at higher doses. Using the differential cell staining of BAL samples with Eosin Y and azur/methylene blue, it was In the case of the PEI-LPEG siRNA nanoparticle-treated groups, both the non-targeting (NT) and anti-CXCL-1 siRNA-treated groups demonstrated 10-fold decreases in the CXCL-1 gene expression compared to the PBS-LPS samples (4-vs. cache = ./cache/cord-298224-flyx85lr.txt txt = ./txt/cord-298224-flyx85lr.txt === reduce.pl bib === id = cord-327568-5vo4nmei author = Tosini, Fabio title = Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection date = 2019-05-15 pages = extension = .txt mime = text/plain words = 7398 sentences = 362 flesch = 52 summary = title: Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection parvum proteins, were tested for their ability to induce immune responses in adult mice and for protection on neonate BALB/c mice born from females immunised by mucosal delivery of both peptides. The IP immunisation of adult BALB/c mice to a single antigen (SA35 or SA40) or to a mixture of the two antigens (SA35/40 mix) induced specific anti-Cryptosporidium IgG in serum after day 14 following initial administration. The mucosal delivery of SA35/40 mix in female BALB/c mice induced specific anti-Cryptosporidium IgG (mainly IgG1) in serum 21 days after initial immunisation. In humans, maternal immunisation with tetanus toxoid has Fig. 9 Quantification of COWP gene DNA copies by qPCR in the intestinal content of neonate mice infected with 5 × 10 3 Cryptosporidium parvum oocysts. cache = ./cache/cord-327568-5vo4nmei.txt txt = ./txt/cord-327568-5vo4nmei.txt === reduce.pl bib === id = cord-356207-tpn5cg4n author = Beniac, Daniel R title = Architecture of the SARS coronavirus prefusion spike date = 2006-07-16 pages = extension = .txt mime = text/plain words = 801 sentences = 48 flesch = 51 summary = The emergence in 2003 of a new coronavirus (CoV) responsible for the atypical pneumonia termed severe acute respiratory syndrome (SARS) was a stark reminder that hitherto unknown viruses have the potential to cross species barriers to become new human pathogens. Here we describe the SARS-CoV 'spike' structure determined by single-particle cryo-EM, along with the docked atomic structures of the receptor-binding domain and prefusion core. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nsmb1123) contains supplementary material, which is available to authorized users. SARS-CoV-enriched fractions were checked by SDS-Page and Western blotting, and rendered non-infectious by irradiation in a gamma cell on dry ice with a 2 Mrad exposure for 90 minutes. Formvar-carbon coated 400-mesh nickel grids were floated on drops of purified SARS-CoV (40μl) for 1 minute. Structure of SARS coronavirus spike receptor-binding domain complexed with receptor Solution structure of the severe acute respiratory syndrome-coronavirus heptad repeat 2 domain in the prefusion state cache = ./cache/cord-356207-tpn5cg4n.txt txt = ./txt/cord-356207-tpn5cg4n.txt === reduce.pl bib === id = cord-295033-5fd9bu60 author = Parma, Y.R. title = Antibodies anti-Shiga toxin 2 B subunit from chicken egg yolk: Isolation, purification and neutralization efficacy date = 2011-09-15 pages = extension = .txt mime = text/plain words = 6045 sentences = 326 flesch = 53 summary = The data suggest that immunization of hens with Stx2B could be a strategy to obtain at low cost a relatively high concentration of anti-Stx2 egg yolk IgY, able to neutralize Stx2 lethal activity. The data suggest that immunization of hens with Stx2B could be a strategy to obtain at low cost a relatively high concentration of anti-Stx2 egg yolk IgY, able to neutralize Stx2 lethal activity. Specific anti-Stx2B polyclonal antibodies obtained from chicken egg yolk and rabbit sera recognized not only the denatured and native form of B subunit, used for immunization but the antibodies were also able to recognize the denatured and native wild type Stx2 holotoxin in western blot (Fig. 3) , indirect ELISA (Fig. 4) and sandwich ELISA (Fig. 5) . In the present report, specific egg yolk IgY antibodies with binding and neutralizing capabilities against the wild type Stx2 toxin were obtained after immunization of laying hens. cache = ./cache/cord-295033-5fd9bu60.txt txt = ./txt/cord-295033-5fd9bu60.txt === reduce.pl bib === id = cord-343409-oao75pzy author = Hayward, Joshua A title = Identification of diverse full-length endogenous betaretroviruses in megabats and microbats date = 2013-03-27 pages = extension = .txt mime = text/plain words = 11603 sentences = 554 flesch = 50 summary = As there were differences in the start position of this ORF in the various group VII bat βERVs (PvERV-βE -I), likely due to random mutation since integration, a nucleotide alignment of the region was generated (Additional file 1: Figure S2 ). To determine if the groupings we had assigned were congruent with known functional differences between retroviruses with respect to betaretroviral RNA nuclear export strategies, we analyzed the bat βERVs, alongside known exogenous and endogenous betaretroviruses, for evidence of motifs indicative of the major export strategies (Additional file 2: Table S4 ). We coupled our analysis of the genomic features of the bat βERVs with the phylogenetic patterns observed in the Gag, Pol, and Env trees (with primacy given to the phylogeny of the highly conserved polymerase sequences) to generate a hypothetical series of events that may have led to the current state of diversity in the genus Betaretrovirus ( Figure 5 ). cache = ./cache/cord-343409-oao75pzy.txt txt = ./txt/cord-343409-oao75pzy.txt === reduce.pl bib === id = cord-333639-usgpe1cz author = Zuwala, Kaja title = Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects date = 2018-04-10 pages = extension = .txt mime = text/plain words = 9337 sentences = 493 flesch = 48 summary = title: Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects We focus on the choice of the macromolecular backbone as a carrier for the conjugated drug and analyze blood coagulation, binding to albumin, albumin aggregation, inhibitory activity on polymerases, and cytotoxicity for polymers differed by their anionic charge (carboxylates, phosphates and phosphonates, sulfonates). As a result, we identify polymers and macromolecular prodrugs that are devoid of blood anti-coagulation activity but are strong as inhibitors of polymerases and efficacious as delivery vehicles for ribavirinthus being attractive for the development of broad-spectrum antiviral agents. This observation echoes our recent findings on the apparent unique pairing of negative character and hydrophobicity of the polymer backbone that renders PEAA an efficacious inhibitor of e.g. hepatitis C virus intracellular replication [55] and a lead polymer with broad-spectrum antiviral activity [21] . Polyanionic macromolecular prodrugs of ribavirin: antiviral agents with a broad Spectrum of activity cache = ./cache/cord-333639-usgpe1cz.txt txt = ./txt/cord-333639-usgpe1cz.txt === reduce.pl bib === id = cord-335121-ro3x3qa3 author = Ingram, George A. title = A comparative assessment of four serological methods used in the detection and measurement of anti-parasite antibodies in the serum of the amphibian, bufo viridis date = 1988-04-30 pages = extension = .txt mime = text/plain words = 3116 sentences = 180 flesch = 50 summary = Abstract Antibodies against Crithidia fasciculata choanomastigotes were detected in green toad (Bufo viridis) sera by direct agglutination, indirect haemagglutination (IHA), complement-fixation test (CFT) and enzyme-linked immunosorbent assay (ELISA), Correlation coefficients (r) were calculated for comparisons between each of the techniques and regression formulae derived in order to convert antibody levels as determined by one immunological method to that of another. In this paper we present the results of acomparative assessment of four serological tests (direct agglutination, indirect haemagglutination, complement-fixation test and ELISA) used to detect and to determine the levels of antibodies in the sera of green toads (B. fasciculata and the number of control and immune sera containing detectable antibodies were the lowest for DA and CFT, intermediate for IHA and highest for the ELISA method (Table 1) . Nevertheless the method of antigen preparation ma> not be a salient criterion for antibody estimation in immune sera because correlation values of over 89% (f'< 0.001) were found when IHA titres were compared to those of ELISA. cache = ./cache/cord-335121-ro3x3qa3.txt txt = ./txt/cord-335121-ro3x3qa3.txt === reduce.pl bib === id = cord-335591-r0x8yaqj author = Ohnishi, Kazuo title = Establishment and Characterization of Monoclonal Antibodies Against SARS Coronavirus date = 2007-11-28 pages = extension = .txt mime = text/plain words = 3126 sentences = 242 flesch = 67 summary = The hybridomas produce monoclonal antibodies that recognize viral component molecules, including the spike protein (S) and the nucleocapsid protein (N), enabling the immunological detection of SARS-CoV by immunofluorescence staining, immunoblot, or an antigen-capture ELISA system. Based on clinical experience, several options have been considered in the quest to develop the capacity to accurately diagnose SARS-CoV infection, including molecular biology techniques and serological tests such as antigen-capture ELISA assay and immunofluorescence assay to detect virus-infected cells in respiratory swabs (3-7) . These mAbs enable the general immunological detection of SARS-CoV by methods such as immunofluorescent staining, immunoblotting, and immunohistology, in addition to the construction of a highly sensitive antigen-capture sandwich ELISA (6). The UV-inactivated purified SARS-CoV samples (see Note 1), which are serially diluted with 1% OVA/PBS-Tween, are added to the wells and incubated for 1 h at room temperature cache = ./cache/cord-335591-r0x8yaqj.txt txt = ./txt/cord-335591-r0x8yaqj.txt ===== Reducing email addresses cord-351498-bmq6zcb0 cord-334165-7gfk554m cord-327568-5vo4nmei Creating transaction Updating adr table ===== Reducing keywords cord-001732-4eyn7pjq cord-003915-kje8lvgl cord-002013-rb9xdzro cord-001017-4qfhltg4 cord-013526-6fip93l2 cord-011106-h20vbmbo cord-009800-tajkpgkj cord-267736-rya9w6sh cord-001065-j4hvyyoi cord-000354-05lnj3w0 cord-013265-qrfi6e5c cord-002583-cgcf7mgj cord-275635-d50bxe7c cord-026866-0hlre9i6 cord-259364-8zoav7b0 cord-259094-5qzbctan cord-264267-weat0qs6 cord-295416-y3lvcjqd cord-338108-3rn6fwx3 cord-274396-l611eisi cord-308461-4lhh3du0 cord-335310-61wibso4 cord-309742-fd1qmr87 cord-303381-xvzhb7ix cord-278802-bverdk5w cord-276732-u2d1z4ip cord-260834-v254de8k cord-277054-eq4obbte cord-273035-sewfb3q8 cord-351498-bmq6zcb0 cord-265740-wjdeps3h cord-275779-ocbygkyb cord-305648-majanu8l cord-292862-ezrkg0dc cord-347661-q9lgliph cord-339694-sp212tai cord-332221-6ea6gz9s cord-334165-7gfk554m cord-340125-il35gs97 cord-298224-flyx85lr cord-327568-5vo4nmei cord-295033-5fd9bu60 cord-333639-usgpe1cz cord-356207-tpn5cg4n cord-343409-oao75pzy cord-335121-ro3x3qa3 cord-335591-r0x8yaqj Creating transaction Updating wrd table ===== Reducing urls cord-001017-4qfhltg4 cord-003915-kje8lvgl cord-013526-6fip93l2 cord-001065-j4hvyyoi cord-013265-qrfi6e5c cord-264267-weat0qs6 cord-338108-3rn6fwx3 cord-274396-l611eisi cord-308461-4lhh3du0 cord-260834-v254de8k cord-265740-wjdeps3h cord-292862-ezrkg0dc cord-298224-flyx85lr cord-343409-oao75pzy Creating transaction Updating url table ===== Reducing named entities cord-002013-rb9xdzro cord-003915-kje8lvgl cord-001732-4eyn7pjq cord-001017-4qfhltg4 cord-011106-h20vbmbo cord-013526-6fip93l2 cord-009800-tajkpgkj cord-001065-j4hvyyoi cord-267736-rya9w6sh cord-000354-05lnj3w0 cord-002583-cgcf7mgj cord-275635-d50bxe7c cord-013265-qrfi6e5c cord-026866-0hlre9i6 cord-259094-5qzbctan cord-259364-8zoav7b0 cord-264267-weat0qs6 cord-338108-3rn6fwx3 cord-295416-y3lvcjqd cord-274396-l611eisi cord-308461-4lhh3du0 cord-309742-fd1qmr87 cord-335310-61wibso4 cord-303381-xvzhb7ix cord-276732-u2d1z4ip cord-278802-bverdk5w cord-260834-v254de8k cord-277054-eq4obbte cord-273035-sewfb3q8 cord-351498-bmq6zcb0 cord-265740-wjdeps3h cord-275779-ocbygkyb cord-305648-majanu8l cord-292862-ezrkg0dc cord-347661-q9lgliph cord-339694-sp212tai cord-332221-6ea6gz9s cord-334165-7gfk554m cord-340125-il35gs97 cord-298224-flyx85lr cord-327568-5vo4nmei cord-295033-5fd9bu60 cord-343409-oao75pzy cord-356207-tpn5cg4n cord-335591-r0x8yaqj cord-333639-usgpe1cz cord-335121-ro3x3qa3 Creating transaction Updating ent table ===== Reducing parts of speech cord-011106-h20vbmbo cord-002013-rb9xdzro cord-003915-kje8lvgl cord-001017-4qfhltg4 cord-001732-4eyn7pjq cord-013526-6fip93l2 cord-009800-tajkpgkj cord-001065-j4hvyyoi cord-267736-rya9w6sh cord-000354-05lnj3w0 cord-002583-cgcf7mgj cord-013265-qrfi6e5c cord-275635-d50bxe7c cord-026866-0hlre9i6 cord-259094-5qzbctan cord-264267-weat0qs6 cord-259364-8zoav7b0 cord-295416-y3lvcjqd cord-338108-3rn6fwx3 cord-274396-l611eisi cord-308461-4lhh3du0 cord-335310-61wibso4 cord-309742-fd1qmr87 cord-303381-xvzhb7ix cord-278802-bverdk5w cord-276732-u2d1z4ip cord-260834-v254de8k cord-277054-eq4obbte cord-273035-sewfb3q8 cord-265740-wjdeps3h cord-305648-majanu8l cord-351498-bmq6zcb0 cord-275779-ocbygkyb cord-347661-q9lgliph cord-334165-7gfk554m cord-332221-6ea6gz9s cord-339694-sp212tai cord-356207-tpn5cg4n cord-340125-il35gs97 cord-292862-ezrkg0dc cord-298224-flyx85lr cord-327568-5vo4nmei cord-335121-ro3x3qa3 cord-335591-r0x8yaqj cord-295033-5fd9bu60 cord-333639-usgpe1cz cord-343409-oao75pzy Creating transaction Updating pos table Building ./etc/reader.txt cord-343409-oao75pzy cord-000354-05lnj3w0 cord-309742-fd1qmr87 cord-309742-fd1qmr87 cord-275779-ocbygkyb cord-308461-4lhh3du0 number of items: 47 sum of words: 287,357 average size in words: 6,113 average readability score: 49 nouns: cells; virus; mice; infection; protein; cell; antibody; group; expression; antibodies; influenza; samples; lung; ml; proteins; control; min; analysis; groups; serum; study; data; vaccine; activity; results; °; lungs; response; entry; antigen; time; mouse; viruses; treatment; gene; studies; levels; concentration; effect; animals; days; responses; inflammation; dna; use; assay; immunization; nanoparticles; buffer; particles verbs: used; shown; followed; infected; contained; compared; induce; performed; binding; treat; indicating; incubated; determine; observed; added; described; obtained; include; increased; based; detected; washed; purified; found; suggest; associated; demonstrate; expressing; reduced; tested; provided; mediated; collected; analyzed; produced; neutralizing; reported; immunized; prepared; evaluated; identify; measured; blocking; caused; revealed; result; remove; enhance; stained; diluted adjectives: anti; human; viral; specific; immune; different; significant; respiratory; non; inflammatory; acute; high; recombinant; higher; similar; clinical; infected; low; positive; cellular; antiviral; single; free; first; pulmonary; lower; negative; severe; total; important; like; dependent; several; experimental; multiple; primary; infectious; previous; naïve; large; protective; early; monoclonal; epithelial; molecular; intestinal; independent; present; additional; major adverbs: also; however; well; previously; significantly; respectively; therefore; highly; prior; overnight; moreover; subsequently; alone; approximately; specifically; briefly; finally; directly; still; furthermore; together; immediately; first; even; interestingly; next; twice; recently; relatively; particularly; mainly; daily; similarly; often; indeed; less; statistically; slightly; rather; likely; currently; much; least; especially; fully; intranasally; widely; orally; long; instead pronouns: we; it; their; our; its; they; i; them; us; itself; your; his; you; iga1; themselves; svlps; one; mg; her; rsa59; imagej; he; siga1; mine; lysate/; igys; iga2; cord-305648-majanu8l; cdc42; a1-antitrypsin proper nouns: PBS; Fig; ELISA; SARS; siRNA; mg; PreF; IAV; PR8; C; MERS; DPP4; PEI; CoV; LPS; T; RNA; IGF1; RSV; C.; sera; IgG; Figure; Rubisco; RT; HA; pH; PCR; USA; S; TGEV; Supplementary; E.; BTV; •; A; B; mL; Sigma; JcDV; Japan; M; DYNA; CoV-2; IAPV; ADCC; L; IgA; WT; Alum keywords: pbs; elisa; cell; sars; virus; lung; antibody; tgev; protein; pr8; mouse; lps; group; dna; x31; type; th1; table; supplementary; supplemental; stx2; snh; sirna; shiga; sds; sa40; sa35; rubisco; rsv; rsa59; rev; response; rbv; ptx3; ptm; ppp; polymer; plate; phage; peptide; pei; peaa; pca; pageia; orf; nanoparticle; mm3-sero; midge; mhv; mhc one topic; one dimension: cells file(s): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828711/ titles(s): Treatment with hyperimmune equine immunoglobulin or immunoglobulin fragments completely protects rodents from Ebola virus infection three topics; one dimension: cells; virus; virus file(s): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068995/, https://doi.org/10.1101/2020.04.15.037564, https://www.ncbi.nlm.nih.gov/pubmed/30988390/ titles(s): Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway | Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment | Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies five topics; three dimensions: virus pbs mice; cells mice entry; antibodies pbs protein; virus cells infection; cells 10 pbs file(s): https://doi.org/10.1101/2020.04.15.037564, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068995/, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296071/, https://doi.org/10.1186/1742-4690-10-35, https://www.ncbi.nlm.nih.gov/pubmed/30988390/ titles(s): Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment | Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway | Prophylactic Activity of Orally Administered FliD-Reactive Monoclonal SIgA Against Campylobacter Infection | Identification of diverse full-length endogenous betaretroviruses in megabats and microbats | Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies Type: cord title: keyword-pbs-cord date: 2021-05-25 time: 15:47 username: emorgan patron: Eric Morgan email: emorgan@nd.edu input: keywords:pbs ==== make-pages.sh htm files ==== make-pages.sh complex files ==== make-pages.sh named enities ==== making bibliographics id: cord-356207-tpn5cg4n author: Beniac, Daniel R title: Architecture of the SARS coronavirus prefusion spike date: 2006-07-16 words: 801 sentences: 48 pages: flesch: 51 cache: ./cache/cord-356207-tpn5cg4n.txt txt: ./txt/cord-356207-tpn5cg4n.txt summary: The emergence in 2003 of a new coronavirus (CoV) responsible for the atypical pneumonia termed severe acute respiratory syndrome (SARS) was a stark reminder that hitherto unknown viruses have the potential to cross species barriers to become new human pathogens. Here we describe the SARS-CoV ''spike'' structure determined by single-particle cryo-EM, along with the docked atomic structures of the receptor-binding domain and prefusion core. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nsmb1123) contains supplementary material, which is available to authorized users. SARS-CoV-enriched fractions were checked by SDS-Page and Western blotting, and rendered non-infectious by irradiation in a gamma cell on dry ice with a 2 Mrad exposure for 90 minutes. Formvar-carbon coated 400-mesh nickel grids were floated on drops of purified SARS-CoV (40μl) for 1 minute. Structure of SARS coronavirus spike receptor-binding domain complexed with receptor Solution structure of the severe acute respiratory syndrome-coronavirus heptad repeat 2 domain in the prefusion state abstract: The emergence in 2003 of a new coronavirus (CoV) responsible for the atypical pneumonia termed severe acute respiratory syndrome (SARS) was a stark reminder that hitherto unknown viruses have the potential to cross species barriers to become new human pathogens. Here we describe the SARS-CoV 'spike' structure determined by single-particle cryo-EM, along with the docked atomic structures of the receptor-binding domain and prefusion core. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nsmb1123) contains supplementary material, which is available to authorized users. url: https://www.ncbi.nlm.nih.gov/pubmed/16845391/ doi: 10.1038/nsmb1123 id: cord-001065-j4hvyyoi author: Boncristiani, Humberto F. title: In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) date: 2013-09-05 words: 6367 sentences: 326 pages: flesch: 47 cache: ./cache/cord-001065-j4hvyyoi.txt txt: ./txt/cord-001065-j4hvyyoi.txt summary: title: In Vitro Infection of Pupae with Israeli Acute Paralysis Virus Suggests Disturbance of Transcriptional Homeostasis in Honey Bees (Apis mellifera) An experimental protocol to test these systems was developed, using injections of Israeli Acute Paralysis Virus (IAPV) into honey bee pupae reared ex-situ under laboratory conditions. Gene expression analyses of three separate experiments suggest IAPV disruption of transcriptional homeostasis of several fundamental cellular functions, including an up-regulation of the ribosomal biogenesis pathway. Little is known about the specific biology of the viruses in these families that infect honey bees, although they contain important bee pathogens, such as Deformed Wing Virus (DWV) and Israeli Acute Paralysis Virus (IAPV). Post-hoc tests of main treatment effects showed significantly higher gene expression in the IAPV-inoculated bees compared to the two control groups for Actin, 28S rRNA, and mGST1. The observed gene expression patterns could be due to viral manipulation of the cells to increase virus replication or present cell compensatory responses to IAPV infection. abstract: The ongoing decline of honey bee health worldwide is a serious economic and ecological concern. One major contributor to the decline are pathogens, including several honey bee viruses. However, information is limited on the biology of bee viruses and molecular interactions with their hosts. An experimental protocol to test these systems was developed, using injections of Israeli Acute Paralysis Virus (IAPV) into honey bee pupae reared ex-situ under laboratory conditions. The infected pupae developed pronounced but variable patterns of disease. Symptoms varied from complete cessation of development with no visual evidence of disease to rapid darkening of a part or the entire body. Considerable differences in IAPV titer dynamics were observed, suggesting significant variation in resistance to IAPV among and possibly within honey bee colonies. Thus, selective breeding for virus resistance should be possible. Gene expression analyses of three separate experiments suggest IAPV disruption of transcriptional homeostasis of several fundamental cellular functions, including an up-regulation of the ribosomal biogenesis pathway. These results provide first insights into the mechanisms of IAPV pathogenicity. They mirror a transcriptional survey of honey bees afflicted with Colony Collapse Disorder and thus support the hypothesis that viruses play a critical role in declining honey bee health. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764161/ doi: 10.1371/journal.pone.0073429 id: cord-001017-4qfhltg4 author: Chatterjee, Dhriti title: Microglia Play a Major Role in Direct Viral-Induced Demyelination date: 2013-06-20 words: 6654 sentences: 312 pages: flesch: 42 cache: ./cache/cord-001017-4qfhltg4.txt txt: ./txt/cord-001017-4qfhltg4.txt summary: Previous studies demonstrated that microglia can be persistently infected by neurotropic mouse hepatitis virus (MHV) which causes meningoencephalitis, myelitis with subsequent axonal loss, and demyelination and serve as a virus-induced model of human neurological disease multiple sclerosis (MS). In our current studies, we have used RSA59 infection in vivo, in vitro, and ex vivo as a model to understand whether MHV can directly infect CNS resident microglia and the mechanism of microglial activation in the induction of chronic demyelination. To confirm the RSA59-induced CNS inflammation, brain and spinal cord sections from day 7 (peak of inflammation) and day 30 (peak of demyelination) postinfected mice were stained with H&E or LFB and examined. While Iba1 immunofluorescence was observed in both gray and white matter, double fluorescence/immunofluorescence demonstrated dual labelling of EGFP (viral antigen) positive Iba1 positive microglia/macrophages were present only in the white matter of RSA59 infected mice (Figure 1 ). abstract: Microglia are the resident macrophage-like populations in the central nervous system (CNS). Microglia remain quiescent, unable to perform effector and antigen presentation (APC) functions until activated by injury or infection, and have been suggested to represent the first line of defence for the CNS. Previous studies demonstrated that microglia can be persistently infected by neurotropic mouse hepatitis virus (MHV) which causes meningoencephalitis, myelitis with subsequent axonal loss, and demyelination and serve as a virus-induced model of human neurological disease multiple sclerosis (MS). Current studies revealed that MHV infection is associated with the pronounced activation of microglia during acute inflammation, as evidenced by characteristic changes in cellular morphology and increased expression of microglia-specific proteins, Iba1 (ionized calcium-binding adaptor molecule 1), which is a macrophage/microglia-specific novel calcium-binding protein and involved in membrane ruffling and phagocytosis. During chronic inflammation (day 30 postinfection), microglia were still present within areas of demyelination. Experiments performed in ex vivo spinal cord slice culture and in vitro neonatal microglial culture confirmed direct microglial infection. Our results suggest that MHV can directly infect and activate microglia during acute inflammation, which in turn during chronic inflammation stage causes phagocytosis of myelin sheath leading to chronic inflammatory demyelination. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3705805/ doi: 10.1155/2013/510396 id: cord-335310-61wibso4 author: Chen, Hui-Wen title: Synthetic virus-like particles prepared via protein corona formation enable effective vaccination in an avian model of coronavirus infection date: 2016-08-15 words: 5482 sentences: 264 pages: flesch: 40 cache: ./cache/cord-335310-61wibso4.txt txt: ./txt/cord-335310-61wibso4.txt summary: Herein, a facile approach to formulate synthetic virus-like particles (sVLPs) is demonstrated by exploiting the phenomenon of protein corona formation induced by the high-energy surfaces of synthetic nanoparticles. As compared to inoculation with free proteins, vaccination with the sVLPs showed enhanced lymphatic antigen delivery, stronger antibody titers, increased splenic T-cell response, and reduced infection-associated symptoms in an avian model of coronavirus infection. Comparison to a commercial whole inactivated virus vaccine also showed evidence of superior antiviral protection by the sVLPs. The study demonstrates a simple yet robust method in bridging viral antigens with synthetic nanoparticles for improved vaccine application; it has practical implications in the management of human viral infections as well as in animal agriculture. In the present study, vaccination with the sVLPs resulted in enhanced humoral and cellular immune responses, improving protection against an avian model of coronavirus infection as compared to free protein antigens and a commercial WIV vaccine. abstract: The ongoing battle against current and rising viral infectious threats has prompted increasing effort in the development of vaccine technology. A major thrust in vaccine research focuses on developing formulations with virus-like features towards enhancing antigen presentation and immune processing. Herein, a facile approach to formulate synthetic virus-like particles (sVLPs) is demonstrated by exploiting the phenomenon of protein corona formation induced by the high-energy surfaces of synthetic nanoparticles. Using an avian coronavirus spike protein as a model antigen, sVLPs were prepared by incubating 100 nm gold nanoparticles in a solution containing an optimized concentration of viral proteins. Following removal of free proteins, antigen-laden particles were recovered and showed morphological semblance to natural viral particles under nanoparticle tracking analysis and transmission electron microscopy. As compared to inoculation with free proteins, vaccination with the sVLPs showed enhanced lymphatic antigen delivery, stronger antibody titers, increased splenic T-cell response, and reduced infection-associated symptoms in an avian model of coronavirus infection. Comparison to a commercial whole inactivated virus vaccine also showed evidence of superior antiviral protection by the sVLPs. The study demonstrates a simple yet robust method in bridging viral antigens with synthetic nanoparticles for improved vaccine application; it has practical implications in the management of human viral infections as well as in animal agriculture. url: https://doi.org/10.1016/j.biomaterials.2016.08.018 doi: 10.1016/j.biomaterials.2016.08.018 id: cord-295416-y3lvcjqd author: Eichinger, Katherine M. title: Prefusion RSV F Immunization Elicits Th2-Mediated Lung Pathology in Mice When Formulated With a Th2 (but Not a Th1/Th2-Balanced) Adjuvant Despite Complete Viral Protection date: 2020-07-29 words: 9392 sentences: 452 pages: flesch: 46 cache: ./cache/cord-295416-y3lvcjqd.txt txt: ./txt/cord-295416-y3lvcjqd.txt summary: These data suggest that in the absence of preimmunity, stabilized PreF antigens may still be associated with aberrant Th2 responses that induce lung pathology in response to RSV infection, and can be prevented by formulation with more Th1/Th2-balanced adjuvants that enhance CD4+ and CD8+ IFNγ+ T cell responses. The objective of this study was to determine the capacity of RSV pre-fusion (PreF) vaccines formulated with different adjuvants to generate neutralizing antibody, prevent virus replication, and protect from pulmonary pathology following RSV challenge. Despite lower neutralizing antibody titers in mice immunized with PreF/Advax-SM, as compared to PreF/Alum, both immunization groups had undetectable RSV in their lungs at 4 dpi ( Figure 1F ). Taken together, these data indicate that RSV PreF immunization formulated with Th1-skewing adjuvants, like Advax-SM, provide protection against RSV infection in naïve BALB/c mice as compared to alum by inhibiting viral replication without eliciting enhanced pulmonary pathology. abstract: Respiratory syncytial virus (RSV) remains the most common cause of lower respiratory tract infections in children worldwide. Development of a vaccine has been hindered by the risk of developing enhanced respiratory disease (ERD) upon natural exposure to the virus. Generation of higher quality neutralizing antibodies with stabilized pre-fusion F protein antigens has been proposed as a strategy to prevent ERD. We sought to test whether there was evidence of ERD in naïve BALB/c mice immunized with an unadjuvanted, stabilized pre-fusion F protein, and challenged with RSV line 19. We further sought to determine the extent to which formulation with a Th2-biased (alum) or a more Th1/Th2-balanced (Advax-SM) adjuvant influenced cellular responses and lung pathology. When exposed to RSV, mice immunized with pre-fusion F protein alone (PreF) exhibited increased airway eosinophilia and mucus accumulation. This was further exacerbated by formulation of PreF with Alum (aluminum hydroxide). Conversely, formulation of PreF with a Th1/Th2-balanced adjuvant, Advax-SM, not only suppressed RSV viral replication, but also inhibited airway eosinophilia and mucus accumulation. This was associated with lower numbers of lung innate lymphocyte cells (ILC2s) and CD4+ T cells producing IL-5+ or IL-13+ and increased IFNγ+ CD4+ and CD8+ T cells, in addition to RSV F-specific CD8+ T cells. These data suggest that in the absence of preimmunity, stabilized PreF antigens may still be associated with aberrant Th2 responses that induce lung pathology in response to RSV infection, and can be prevented by formulation with more Th1/Th2-balanced adjuvants that enhance CD4+ and CD8+ IFNγ+ T cell responses. This may support the use of stabilized PreF antigens with Th1/Th2-balanced adjuvants like, Advax-SM, as safer alternatives to alum in RSV vaccine candidates. url: https://doi.org/10.3389/fimmu.2020.01673 doi: 10.3389/fimmu.2020.01673 id: cord-343409-oao75pzy author: Hayward, Joshua A title: Identification of diverse full-length endogenous betaretroviruses in megabats and microbats date: 2013-03-27 words: 11603 sentences: 554 pages: flesch: 50 cache: ./cache/cord-343409-oao75pzy.txt txt: ./txt/cord-343409-oao75pzy.txt summary: As there were differences in the start position of this ORF in the various group VII bat βERVs (PvERV-βE -I), likely due to random mutation since integration, a nucleotide alignment of the region was generated (Additional file 1: Figure S2 ). To determine if the groupings we had assigned were congruent with known functional differences between retroviruses with respect to betaretroviral RNA nuclear export strategies, we analyzed the bat βERVs, alongside known exogenous and endogenous betaretroviruses, for evidence of motifs indicative of the major export strategies (Additional file 2: Table S4 ). We coupled our analysis of the genomic features of the bat βERVs with the phylogenetic patterns observed in the Gag, Pol, and Env trees (with primacy given to the phylogeny of the highly conserved polymerase sequences) to generate a hypothetical series of events that may have led to the current state of diversity in the genus Betaretrovirus ( Figure 5 ). abstract: BACKGROUND: Betaretroviruses infect a wide range of species including primates, rodents, ruminants, and marsupials. They exist in both endogenous and exogenous forms and are implicated in animal diseases such as lung cancer in sheep, and in human disease, with members of the human endogenous retrovirus-K (HERV-K) group of endogenous betaretroviruses (βERVs) associated with human cancers and autoimmune diseases. To improve our understanding of betaretroviruses in an evolutionarily distinct host species, we characterized βERVs present in the genomes and transcriptomes of mega- and microbats, which are an important reservoir of emerging viruses. RESULTS: A diverse range of full-length βERVs were discovered in mega- and microbat genomes and transcriptomes including the first identified intact endogenous retrovirus in a bat. Our analysis revealed that the genus Betaretrovirus can be divided into eight distinct sub-groups with evidence of cross-species transmission. Betaretroviruses are revealed to be a complex retrovirus group, within which one sub-group has evolved from complex to simple genomic organization through the acquisition of an env gene from the genus Gammaretrovirus. Molecular dating suggests that bats have contended with betaretroviral infections for over 30 million years. CONCLUSIONS: Our study reveals that a diverse range of betaretroviruses have circulated in bats for most of their evolutionary history, and cluster with extant betaretroviruses of divergent mammalian lineages suggesting that their distribution may be largely unrestricted by host species barriers. The presence of βERVs with the ability to transcribe active viral elements in a major animal reservoir for viral pathogens has potential implications for public health. url: https://doi.org/10.1186/1742-4690-10-35 doi: 10.1186/1742-4690-10-35 id: cord-298224-flyx85lr author: Hibbitts, Alan J. title: In Vitro and In Vivo Assessment of PEGylated PEI for Anti-IL-8/CxCL-1 siRNA Delivery to the Lungs date: 2020-06-27 words: 11340 sentences: 633 pages: flesch: 56 cache: ./cache/cord-298224-flyx85lr.txt txt: ./txt/cord-298224-flyx85lr.txt summary: Following optimization with antiglyceraldehyde 3-phosphate dehydrogenase (GAPDH) siRNA, PEI and PEI-LPEG anti-IL8 siRNA nanoparticles were assessed for efficacy using polarised Calu-3 human airway epithelial cells and a twin stage impinger (TSI) in vitro lung model. This work demonstrates the potential of nebulised PEI-PEG siRNA nanoparticles in modulating pulmonary inflammation and highlights the need to move towards more relevant in vitro and in vivo models for respiratory drug development. In contrast, the nebulised PEI-LPEG siRNA nanoparticles demonstrated significantly greater levels of GAPDH knockdown versus the PBS-treated controls at higher doses. Using the differential cell staining of BAL samples with Eosin Y and azur/methylene blue, it was In the case of the PEI-LPEG siRNA nanoparticle-treated groups, both the non-targeting (NT) and anti-CXCL-1 siRNA-treated groups demonstrated 10-fold decreases in the CXCL-1 gene expression compared to the PBS-LPS samples (4-vs. abstract: Inhalation offers a means of rapid, local delivery of siRNA to treat a range of autoimmune or inflammatory respiratory conditions. This work investigated the potential of a linear 10 kDa Poly(ethylene glycol) (PEG)-modified 25 kDa branched polyethyleneimine (PEI) (PEI-LPEG) to effectively deliver siRNA to airway epithelial cells. Following optimization with anti- glyceraldehyde 3-phosphate dehydrogenase (GAPDH) siRNA, PEI and PEI-LPEG anti-IL8 siRNA nanoparticles were assessed for efficacy using polarised Calu-3 human airway epithelial cells and a twin stage impinger (TSI) in vitro lung model. Studies were then advanced to an in vivo lipopolysaccharide (LPS)-stimulated rodent model of inflammation. In parallel, the suitability of the siRNA-loaded nanoparticles for nebulization using a vibrating mesh nebuliser was assessed. The siRNA nanoparticles were nebulised using an Aerogen(®) Pro vibrating mesh nebuliser and characterised for aerosol output, droplet size and fine particle fraction. Only PEI anti-IL8 siRNA nanoparticles were capable of significant levels of IL-8 knockdown in vitro in non-nebulised samples. However, on nebulization through a TSI, only PEI-PEG siRNA nanoparticles demonstrated significant decreases in gene and protein expression in polarised Calu-3 cells. In vivo, both anti-CXCL-1 (rat IL-8 homologue) nanoparticles demonstrated a decreased CXCL-1 gene expression in lung tissue, but this was non-significant. However, PEI anti-CXCL-1 siRNA-treated rats were found to have significantly less infiltrating macrophages in their bronchoalveolar lavage (BAL) fluid. Overall, the in vivo gene and protein inhibition findings indicated a result more reminiscent of the in vitro bolus delivery rather than the in vitro nebulization data. This work demonstrates the potential of nebulised PEI-PEG siRNA nanoparticles in modulating pulmonary inflammation and highlights the need to move towards more relevant in vitro and in vivo models for respiratory drug development. url: https://www.ncbi.nlm.nih.gov/pubmed/32605011/ doi: 10.3390/nano10071248 id: cord-335121-ro3x3qa3 author: Ingram, George A. title: A comparative assessment of four serological methods used in the detection and measurement of anti-parasite antibodies in the serum of the amphibian, bufo viridis date: 1988-04-30 words: 3116 sentences: 180 pages: flesch: 50 cache: ./cache/cord-335121-ro3x3qa3.txt txt: ./txt/cord-335121-ro3x3qa3.txt summary: Abstract Antibodies against Crithidia fasciculata choanomastigotes were detected in green toad (Bufo viridis) sera by direct agglutination, indirect haemagglutination (IHA), complement-fixation test (CFT) and enzyme-linked immunosorbent assay (ELISA), Correlation coefficients (r) were calculated for comparisons between each of the techniques and regression formulae derived in order to convert antibody levels as determined by one immunological method to that of another. In this paper we present the results of acomparative assessment of four serological tests (direct agglutination, indirect haemagglutination, complement-fixation test and ELISA) used to detect and to determine the levels of antibodies in the sera of green toads (B. fasciculata and the number of control and immune sera containing detectable antibodies were the lowest for DA and CFT, intermediate for IHA and highest for the ELISA method (Table 1) . Nevertheless the method of antigen preparation ma> not be a salient criterion for antibody estimation in immune sera because correlation values of over 89% (f''< 0.001) were found when IHA titres were compared to those of ELISA. abstract: Abstract Antibodies against Crithidia fasciculata choanomastigotes were detected in green toad (Bufo viridis) sera by direct agglutination, indirect haemagglutination (IHA), complement-fixation test (CFT) and enzyme-linked immunosorbent assay (ELISA), Correlation coefficients (r) were calculated for comparisons between each of the techniques and regression formulae derived in order to convert antibody levels as determined by one immunological method to that of another. The highest mean titre obtained by ELISA was approximately 1.5–3.5 times greater than those obtained by the other techniques whilst CFT gave the lowest values. IHA and ELISA titres were affected by different preparations of the crithidial antigen extracts. Highly significant r values were determined for control sera when IHA was compared to ELISA (r > 0.79), and to both CFT and ELISA with immune animals (r > 0.96). ELISA would seem most applicable for screening other lower vertebrates for anti-parasite antibodies especially in areas of human disease prevalence. url: https://api.elsevier.com/content/article/pii/0020751988901476 doi: 10.1016/0020-7519(88)90147-6 id: cord-013265-qrfi6e5c author: Isono, Toshihito title: Treatment of severe pneumonia by hinokitiol in a murine antimicrobial-resistant pneumococcal pneumonia model date: 2020-10-15 words: 4585 sentences: 252 pages: flesch: 38 cache: ./cache/cord-013265-qrfi6e5c.txt txt: ./txt/cord-013265-qrfi6e5c.txt summary: To evaluate the efficacy of repeated hinokitiol administration in a pneumonia mouse model, all mice were intratracheally infected with S. Here, compared with PBS injection, intratracheal administration of 500 μg/mL hinokitiol in a pneumococcal pneumonia mouse model decreased inflammatory cell migration and prevented destruction of alveolar tissue (Fig 2) . However, in clinical settings, antimicrobial agents are administrated several times for the treatment of pneumococcal pneumonia, and thus, we next sought to investigate whether repeated hinokitiol injection decreased the bacterial load in (Fig 7; P < 0.05) . The present study showed that intratracheal administration of hinokitiol decreased the bacterial load in a mouse pneumonia model regardless of macrolide resistance of S. In this study, intratracheal hinokitiol administration reduced neutrophil infiltration and elastase release in the lungs of pneumonia mice, consequently diminishing lung injury and pneumococcal DNA detection in serum. abstract: Streptococcus pneumoniae is often isolated from patients with community-acquired pneumonia. Antibiotics are the primary line of treatment for pneumococcal pneumonia; however, rising antimicrobial resistance is becoming more prevalent. Hinokitiol, which is isolated from trees in the cypress family, has been demonstrated to exert antibacterial activity against S. pneumoniae in vitro regardless of antimicrobial resistance. In this study, the efficacy of hinokitiol was investigated in a mouse pneumonia model. Male 8-week-old BALB/c mice were intratracheally infected with S. pneumoniae strains D39 (antimicrobial susceptible) and NU4471 (macrolide resistant). After 1 h, hinokitiol was injected via the tracheal route. Hinokitiol significantly decreased the number of S. pneumoniae in the bronchoalveolar lavage fluid (BALF) and the concentration of pneumococcal DNA in the serum, regardless of whether bacteria were resistant or susceptible to macrolides. In addition, hinokitiol decreased the infiltration of neutrophils in the lungs, as well as the concentration of inflammatory cytokines in the BALF and serum. Repeated hinokitiol injection at 18 h intervals showed downward trend in the number of S. pneumoniae in the BALF and the concentration of S. pneumoniae DNA in the serum with the number of hinokitiol administrations. These findings suggest that hinokitiol reduced bacterial load and suppressed excessive host immune response in the pneumonia mouse model. Accordingly, hinokitiol warrants further exploration as a potential candidate for the treatment of pneumococcal pneumonia. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561173/ doi: 10.1371/journal.pone.0240329 id: cord-340125-il35gs97 author: Jayapal, Manikandan title: Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses date: 2006-08-16 words: 7377 sentences: 380 pages: flesch: 48 cache: ./cache/cord-340125-il35gs97.txt txt: ./txt/cord-340125-il35gs97.txt summary: title: Genome-wide gene expression profiling of human mast cells stimulated by IgE or FcεRI-aggregation reveals a complex network of genes involved in inflammatory responses A substantial number of genes were regulated by IgE sensitization alone; and following FcεRI aggregation, a wide range of genes were triggered, including genes for cytokines, chemokines, transcription factors, anti-apoptosis, and several genes involved in innate and acquired immunity. Other than these, several genes coding for other receptors involved in immune-responses; immunoregulatory genes; adhesion and/or cytoskeleton remodeling; regulators of apoptosis; signal transduction; transcription factors; were also upregulated by monomeric IgE (Table. Here we studied, whether monomeric-IgE alone, may activate FcεRI intracellular signaling pathways, leading to physiological responses of mast cells, by analyzing the overall tyrosine phosphorylation; fluctuations in cytosolic Ca 2+ concentration; and degranulation by measuring β-hexosaminidase release (Fig. 6A,B &6C) . abstract: BACKGROUND: Mast cells are well established effectors of IgE-triggered allergic reactions and immune responses to parasitic infections. Recent studies indicate that mast cells may play roles in adaptive and innate immunity, suggesting an innovative view of the regulation of immune responses. Here, we profiled the transcriptome of human mast cells sensitized with IgE alone, or stimulated by FcεRI aggregation. RESULTS: Our data show that among 8,793 genes examined, 559 genes are differentially regulated in stimulated mast cells when compared with resting/unstimulated mast cells. The major functional categories of upregulated genes include cytokines, chemokines, and other genes involved in innate and adaptive immune-responses. We observed the increased expression of over 63 gene-transcripts following IgE-sensitization alone. Our data was validated using Real-Time-PCR; ELISA and western blot. We confirmed that IgE alone does not trigger mast cell-immediate responses, such as calcium signals, degranulation or protein-phosphorylation. CONCLUSION: This report represents a substantial advance in our understanding of the genome wide effects triggered by "passive sensitization" or active stimulation of human mast cells, supporting mast cells' potential involvement in a wide range of inflammatory responses. url: https://www.ncbi.nlm.nih.gov/pubmed/16911805/ doi: 10.1186/1471-2164-7-210 id: cord-339694-sp212tai author: Jiang, Xinpeng title: A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection date: 2016-03-28 words: 6818 sentences: 358 pages: flesch: 44 cache: ./cache/cord-339694-sp212tai.txt txt: ./txt/cord-339694-sp212tai.txt summary: title: A phase trial of the oral Lactobacillus casei vaccine polarizes Th2 cell immunity against transmissible gastroenteritis coronavirus infection casei) vaccine against anti-transmissible gastroenteritis virus developed in our laboratory was used to study mucosal immune responses. We found that the recombinant Lactobacillus stimulated IL-17 expression in both the systemic and mucosal immune responses against TGEV infection. Following infection with virulent transmissible gastroenteritis coronavirus, isolated mesenteric lymph node CD4+ T cells mounted a specific proliferative response against infectious or inactivated purified virus upon secondary in vitro stimulation (Anton et al. Here, an oral Lactobacillus casei vaccine against anti-transmissible gastroenteritis virus developed in our laboratory was used to study the mucosal immune response (Jiang et al. In conclusion, our study suggests that the recombinant Lactobacillus vaccine provokes specific mucosal and systemic immune responses to protect piglets from infection. abstract: Transmissible gastroenteritis coronavirus (TGEV) is a member of the genus Coronavirus, family Coronaviridae, order Nidovirales. TGEV is an enteropathogenic coronavirus that causes highly fatal acute diarrhoea in newborn pigs. An oral Lactobacillus casei (L. casei) vaccine against anti-transmissible gastroenteritis virus developed in our laboratory was used to study mucosal immune responses. In this L. casei vaccine, repetitive peptides expressed by L. casei (specifically the MDP and tuftsin fusion protein (MT)) were repeated 20 times and the D antigenic site of the TGEV spike (S) protein was repeated 6 times. Immunization with recombinant Lactobacillus is crucial for investigations of the effect of immunization, such as the first immunization time and dose. The first immunization is more important than the last immunization in the series. The recombinant Lactobacillus elicited specific systemic and mucosal immune responses. Recombinant L. casei had a strong potentiating effect on the cellular immunity induced by the oral L. casei vaccine. However, during TGEV infection, the systemic and local immune responses switched from Th1 to Th2-based immune responses. The systemic humoral immune response was stronger than the cellular immune response after TGEV infection. We found that the recombinant Lactobacillus stimulated IL-17 expression in both the systemic and mucosal immune responses against TGEV infection. Furthermore, the Lactobacillus vaccine stimulated an anti-TGEV infection Th17 pathway. The histopathological examination showed tremendous potential for recombinant Lactobacillus to enable rapid and effective treatment for TGEV with an intestinal tropism in piglets. The TGEV immune protection was primarily dependent on mucosal immunity. url: https://www.ncbi.nlm.nih.gov/pubmed/27020282/ doi: 10.1007/s00253-016-7424-9 id: cord-338108-3rn6fwx3 author: Jin, Yi title: Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection date: 2013-09-18 words: 3969 sentences: 242 pages: flesch: 50 cache: ./cache/cord-338108-3rn6fwx3.txt txt: ./txt/cord-338108-3rn6fwx3.txt summary: title: Immunomodulatory Activity and Protective Effects of Polysaccharide from Eupatorium adenophorum Leaf Extract on Highly Pathogenic H5N1 Influenza Infection In this study, we evaluated the immunomodulatory activities and protective effect of Eupatorium adenophorum polysaccharide (EAP) against the highly pathogenic H5N1 subtype influenza virus. EAP treatment significantly increased the production of IL-6, TNF-α, and IFN-γ both in vivo and in vitro as measured by qPCR and ELISA. In a mouse infection model, intranasal administration of EAP at a dose of 25 mg/kg body weight prior to H5N1 viral challenge efficiently inhibited viral replication, decreased lung lesions, and increased survival rate. To detect IL-6, TNF-, and IFN-expression, lungs of five mice per group were collected at day 0 before infection and tested by qPCR and ELISA. In this study, we evaluated the immunomodulatory activities and protective effect of EAP against H5N1 influenza infection in a mouse model. abstract: The development of novel broad-spectrum, antiviral agents against H5N1 infection is urgently needed. In this study, we evaluated the immunomodulatory activities and protective effect of Eupatorium adenophorum polysaccharide (EAP) against the highly pathogenic H5N1 subtype influenza virus. EAP treatment significantly increased the production of IL-6, TNF-α, and IFN-γ both in vivo and in vitro as measured by qPCR and ELISA. In a mouse infection model, intranasal administration of EAP at a dose of 25 mg/kg body weight prior to H5N1 viral challenge efficiently inhibited viral replication, decreased lung lesions, and increased survival rate. We further evaluated the innate immune recognition of EAP, as this process is regulated primarily Dectin-1 and mannose receptor (MR). These results indicate that EAP may have immunomodulatory properties and a potential prophylactic effect against H5N1 influenza infection. Our investigation suggests an alternative strategy for the development of novel antiinfluenza agents and benefits of E. adenophorum products. url: https://doi.org/10.1155/2013/194976 doi: 10.1155/2013/194976 id: cord-267736-rya9w6sh author: Kang, Xiaoping title: Development of an ELISA-array for simultaneous detection of five encephalitis viruses date: 2012-02-27 words: 2990 sentences: 178 pages: flesch: 47 cache: ./cache/cord-267736-rya9w6sh.txt txt: ./txt/cord-267736-rya9w6sh.txt summary: The ELISA-array assay is based on a "sandwich" ELISA format and consists of viral antibodies printed directly on 96-well microtiter plates, allowing for direct detection of 5 viruses. The developed ELISA-array proved to have similar specificity and higher sensitivity compared with the conventional ELISAs. This method was validated by different viral cultures and three chicken eggs inoculated with infected patient serum. The results demonstrated that this method combined the advantage of ELISA and protein array (multiplex and ease of use) and has potential for the identification of clinical encephalitis virus. When spotting, different spotting buffers and concentrations of capture monoclonal antibodies were evaluated to optimize the ELISA-array assay. To verify the results tested by ELISA-array, RNA extracted from chicken eggs was applied to a real time-RT-PCR assay using primers and probes targeting TBEV. In this study, we developed a multiplex ELISA-based method in a double-antibody sandwich format for the simultaneous detection of five encephalitis-associated viral pathogens. abstract: Japanese encephalitis virus(JEV), tick-borne encephalitis virus(TBEV), and eastern equine encephalitis virus (EEEV) can cause symptoms of encephalitis. Establishment of accurate and easy methods by which to detect these viruses is essential for the prevention and treatment of associated infectious diseases. Currently, there are still no multiple antigen detection methods available clinically. An ELISA-array, which detects multiple antigens, is easy to handle, and inexpensive, has enormous potential in pathogen detection. An ELISA-array method for the simultaneous detection of five encephalitis viruses was developed in this study. Seven monoclonal antibodies against five encephalitis-associated viruses were prepared and used for development of the ELISA-array. The ELISA-array assay is based on a "sandwich" ELISA format and consists of viral antibodies printed directly on 96-well microtiter plates, allowing for direct detection of 5 viruses. The developed ELISA-array proved to have similar specificity and higher sensitivity compared with the conventional ELISAs. This method was validated by different viral cultures and three chicken eggs inoculated with infected patient serum. The results demonstrated that the developed ELISA-array is sensitive and easy to use, which would have potential for clinical use. url: https://www.ncbi.nlm.nih.gov/pubmed/22369052/ doi: 10.1186/1743-422x-9-56 id: cord-273035-sewfb3q8 author: Kang, Xixiong title: Proteomic Fingerprints for Potential Application to Early Diagnosis of Severe Acute Respiratory Syndrome date: 2005-01-01 words: 4128 sentences: 177 pages: flesch: 50 cache: ./cache/cord-273035-sewfb3q8.txt txt: ./txt/cord-273035-sewfb3q8.txt summary: Background: Definitive early-stage diagnosis of severe acute respiratory syndrome (SARS) is important despite the number of laboratory tests that have been developed to complement clinical features and epidemiologic data in case definition. Results: The discriminatory classifier with a panel of four biomarkers determined in the training set could precisely detect 36 of 37 (sensitivity, 97.3%) acute SARS and 987 of 993 (specificity, 99.4%) non-SARS samples. We established a decision tree algorithm consisting of four unique biomarkers for acute SARS in the training set and subsequently validated the accuracy of this classifier by use of a completely blinded test set. To identify the serum biomarkers that could distinguish SARS from non-SARS samples, we used a training set of specimens (37 SARS acute and 74 controls; Tables 1 and 2) and constructed the decision tree classification algorithm using 10 989 peaks [99 peaks ϫ (37 ϩ 74) spectra] of statistical significance identified in the low energy readings (see Materials and Methods). abstract: Background: Definitive early-stage diagnosis of severe acute respiratory syndrome (SARS) is important despite the number of laboratory tests that have been developed to complement clinical features and epidemiologic data in case definition. Pathologic changes in response to viral infection might be reflected in proteomic patterns in sera of SARS patients. Methods: We developed a mass spectrometric decision tree classification algorithm using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry. Serum samples were grouped into acute SARS (n = 74; <7 days after onset of fever) and non-SARS [n = 1067; fever and influenza A (n = 203), pneumonia (n = 176); lung cancer (n = 29); and healthy controls (n = 659)] cohorts. Diluted samples were applied to WCX-2 ProteinChip arrays (Ciphergen), and the bound proteins were assessed on a ProteinChip Reader (Model PBS II). Bioinformatic calculations were performed with Biomarker Wizard software 3.1.1 (Ciphergen). Results: The discriminatory classifier with a panel of four biomarkers determined in the training set could precisely detect 36 of 37 (sensitivity, 97.3%) acute SARS and 987 of 993 (specificity, 99.4%) non-SARS samples. More importantly, this classifier accurately distinguished acute SARS from fever and influenza with 100% specificity (187 of 187). Conclusions: This method is suitable for preliminary assessment of SARS and could potentially serve as a useful tool for early diagnosis. url: https://www.ncbi.nlm.nih.gov/pubmed/15550479/ doi: 10.1373/clinchem.2004.032458 id: cord-277054-eq4obbte author: Kaur, Manpreet title: Rabies DNA vaccine: No impact of MHC Class I and Class II targeting sequences on immune response and protection against lethal challenge date: 2009-03-26 words: 6906 sentences: 378 pages: flesch: 45 cache: ./cache/cord-277054-eq4obbte.txt txt: ./txt/cord-277054-eq4obbte.txt summary: The potency of modified DNA vaccines assessed by total antibody response, antibody isotypes, cytokine profile, neutralizing antibody titer and protection conferred against in vivo challenge; was enhanced in comparison to native unmodified vaccine, but the response elicited did not pertain to the type of target sequence and the directed arm of immunity. The ability of these DNA vaccines to elicit protective responses in immunized mice was assessed by intracerebral challenge with 20 LD 50 of virulent rabies virus CVS strain. In an effort to develop an optimal DNA vaccine against rabies virus, this study was aimed at evaluating the immune enhancement potential of different antigen targeting strategies to selectively improve responses mediated by CD8 + and CD4 + T lymphocytes and by antibodies, induced after intramuscular immunization with DNA plasmids. also reported that DNA vaccine encoding rabies virus glycoprotein lacking transmembrane domain though enhances antibody response but does not confer protection [35] . abstract: Rabies is progressive fatal encephalitis. WHO estimates 55,000 rabies deaths and more than 10 million PEP every year world-wide. A variety of cell-culture derived vaccines are available for prophylaxis against rabies. However, their high cost restricts their usage in developing countries, where such cases are most often encountered. This is driving the quest for newer vaccine formulations; DNA vaccines being most promising amongst them. Here, we explored strategies of antigen trafficking to various cellular compartments aiming at improving both humoral and cellular immunity. These strategies include use of signal sequences namely Tissue Plasminogen Activator (TPA), Ubiquitin (UQ) and Lysosomal-Associated Membrane Protein-1 (LAMP-1). TPA, LAMP-1 and their combination were aimed at enhancing the CD4(+) T cell and antibody response. In contrast, the UQ tag was utilized for enhancing CD8(+) response. The potency of modified DNA vaccines assessed by total antibody response, antibody isotypes, cytokine profile, neutralizing antibody titer and protection conferred against in vivo challenge; was enhanced in comparison to native unmodified vaccine, but the response elicited did not pertain to the type of target sequence and the directed arm of immunity. Interestingly, the DNA vaccines that had been designed to generate different type of immune responses yielded in effect similar response. In conclusion, our data indicate that the directing target sequence is not the exclusive deciding factor for type and extent of immune response elicited and emphasizes on the antigen dependence of immune enhancement strategies. url: https://www.sciencedirect.com/science/article/pii/S0264410X0900200X doi: 10.1016/j.vaccine.2009.01.128 id: cord-264267-weat0qs6 author: Kleine-Weber, Hannah title: Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus date: 2020-01-21 words: 7200 sentences: 325 pages: flesch: 47 cache: ./cache/cord-264267-weat0qs6.txt txt: ./txt/cord-264267-weat0qs6.txt summary: Four polymorphisms (K267E, K267N, A291P and Δ346-348) strongly reduced binding of MERS-CoV S to DPP4 and S protein-driven host cell entry, as determined using soluble S protein and S protein bearing rhabdoviral vectors, respectively. For host cell entry, the surface unit, S1, of MERS-CoV S binds to the cellular type-II transmembrane protein dipeptidyl peptidase 4 (DPP4, CD26) [15] . For the binding studies with solMERS-S1-Fc, a similar protocol was followed as described for the analysis of DPP4 surface expression with the exceptions that sol-MERS-S1-Fc was used instead of the primary antibody (1:10 dilution in PBS/BSA) and that an AlexaFluor488conjugated anti-human antibody (goat, 1:500 dilution in PBS/BSA, ThermoFisher Scientific) was employed as the secondary antibody. Reduced MERS-CoV S-driven host cell entry is caused by inefficient S protein binding to DPP4 harboring polymorphic amino acid residues. abstract: Middle East respiratory syndrome (MERS) coronavirus (MERS-CoV) causes a severe respiratory disease in humans. The MERS-CoV spike (S) glycoprotein mediates viral entry into target cells. For this, MERS-CoV S engages the host cell protein dipeptidyl peptidase 4 (DPP4, CD26) and the interface between MERS-CoV S and DPP4 has been resolved on the atomic level. Here, we asked whether naturally-occurring polymorphisms in DPP4, that alter amino acid residues required for MERS-CoV S binding, influence cellular entry of MERS-CoV. By screening of public databases, we identified fourteen such polymorphisms. Introduction of the respective mutations into DPP4 revealed that all except one (Δ346-348) were compatible with robust DPP4 expression. Four polymorphisms (K267E, K267N, A291P and Δ346-348) strongly reduced binding of MERS-CoV S to DPP4 and S protein-driven host cell entry, as determined using soluble S protein and S protein bearing rhabdoviral vectors, respectively. Two polymorphisms (K267E and A291P) were analyzed in the context of authentic MERS-CoV and were found to attenuate viral replication. Collectively, we identified naturally-occurring polymorphisms in DPP4 that negatively impact cellular entry of MERS-CoV and might thus modulate MERS development in infected patients. url: https://doi.org/10.1080/22221751.2020.1713705 doi: 10.1080/22221751.2020.1713705 id: cord-013526-6fip93l2 author: Labadie, Thomas title: A non-enveloped arbovirus released in lysosome-derived extracellular vesicles induces super-infection exclusion date: 2020-10-19 words: 8084 sentences: 379 pages: flesch: 51 cache: ./cache/cord-013526-6fip93l2.txt txt: ./txt/cord-013526-6fip93l2.txt summary: Here we used Bluetongue virus (BTV) as a model of a non-enveloped arthropod-borne virus and discovered that the majority of viruses are released in EVs. Based on the cellular proteins detected in these EVs, and use of inhibitors targeting the cellular degradation process, we demonstrated that these extracellular vesicles are derived from secretory lysosomes, in which the acidic pH is neutralized upon the infection. Virus released in secretory lysosomes infectious EVs. However, inhibition of autophagosome-lysosome fusion with chloroquine (CQ), led to a significant reduction of infectious EVs released as compared to the control ( Fig 2B) , indicating that the late steps of autophagy are necessary for infectious EVs. In addition, inhibition of MVBs regulator protein HSP90 using geldanamycin in BTV-infected cells (MOI = 10) also led to a significant reduction of infectivity measured in the EVs fraction, as compared to the control, indicating a possible role for MVBs in the release of infectious EVs. In contrast, GW4869, a drug that inhibits the release of exosomes (small vesicles~200nm) derived from MVBs, did not affect the secretion levels of EVs containing BTV ( Fig 2B) . abstract: Recent developments on extracellular vesicles (EVs) containing multiple virus particles challenge the rigid definition of non-enveloped viruses. However, how non-enveloped viruses hijack cell machinery to promote non-lytic release in EVs, and their functional roles, remain to be clarified. Here we used Bluetongue virus (BTV) as a model of a non-enveloped arthropod-borne virus and discovered that the majority of viruses are released in EVs. Based on the cellular proteins detected in these EVs, and use of inhibitors targeting the cellular degradation process, we demonstrated that these extracellular vesicles are derived from secretory lysosomes, in which the acidic pH is neutralized upon the infection. Moreover, we report that secreted EVs are more efficient than free-viruses for initiating infections, but that they trigger super-infection exclusion that only free-viruses can overcome. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595637/ doi: 10.1371/journal.ppat.1009015 id: cord-332221-6ea6gz9s author: Li, Guiping title: Insulin-Like Growth Factor 1 Regulates Acute Inflammatory Lung Injury Mediated by Influenza Virus Infection date: 2019-11-26 words: 6779 sentences: 332 pages: flesch: 50 cache: ./cache/cord-332221-6ea6gz9s.txt txt: ./txt/cord-332221-6ea6gz9s.txt summary: The expression of inflammatory cytokines in the serum was detected by enzyme linked immunosorbent assay; lung injury was observed by hematoxylin-eosin staining; the viral proliferation in the lung was detected by real-time quantitative PCR; and the protein expression of the main molecules in the phosphatidylinositol-3-kinases/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signaling pathways was detected by Western blot. The expression of inflammatory cytokines in the serum was detected by enzyme linked immunosorbent assay; lung injury was observed by hematoxylin-eosin staining; the viral proliferation in the lung was detected by real-time quantitative PCR; and the protein expression of the main molecules in the phosphatidylinositol-3-kinases/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signaling pathways was detected by Western blot. To explore the mechanism by which IGF1 regulates acute inflammatory lung injury induced by IAV infection, a Western blot was used to detect the expression of molecules in key signaling pathways in the lung tissue of PR8-infected mice (50LD 50 PR8). abstract: The acute inflammatory lung injury is an important cause of death due to influenza A virus (IAV) infection. Insulin-like growth factor 1 (IGF1) played an important role in the regulation of inflammation in the immune system. To investigate the role of IGF1 in IAV-mediated acute inflammatory lung injury, the expression of IGF1 and inflammatory cytokines was tested after IAV A/Puerto Rico/8/1934 (H1N1; abbreviated as PR8) infection in A549 cells. Then, a BALB/c mouse model of PR8 infection was established. On days 3, 5, 7, and 9 post-infection, the mice lung tissue was collected to detect the expression changes in IGF1 mRNA and protein. The mice were divided into four groups: (1) PBS (abbreviation of phosphate buffered saline); (2) PR8 + PBS; (3) PR8 + IGF1; and (4) PR8 + PPP (abbreviation of picropodophyllin, the IGF1 receptor inhibitor). The body weight and survival rate of the mice were monitored daily, and the clinical symptoms of the mice were recorded. On day 5 post-infection, the mice were sacrificed to obtain the serum and lung tissues. The expression of inflammatory cytokines in the serum was detected by enzyme linked immunosorbent assay; lung injury was observed by hematoxylin-eosin staining; the viral proliferation in the lung was detected by real-time quantitative PCR; and the protein expression of the main molecules in the phosphatidylinositol-3-kinases/protein kinase B (PI3K/AKT) and mitogen-activated protein kinase (MAPK) signaling pathways was detected by Western blot. It was found that IGF1 expression is upregulated in A549 cells and BALB/c mice infected with PR8, whereas IGF1 regulated the expression of inflammatory cytokines induced by PR8 infection. Overexpression of IGF1 aggravated the IAV-mediated inflammatory response, whereas the inhibition of IGF1 receptor reduced such inflammatory response. The phosphorylation of IGF1 receptor triggered the PI3K/AKT and MAPK signaling pathways to induce an inflammatory response after IAV infection. Therefore, IGF1 plays an important immune function in IAV-mediated acute inflammatory lung injury. IGF1 may provide a therapeutic target for humans in response to an influenza outbreak, and inhibition of IGF1 or IGF1 receptor may represent a novel approach to influenza treatment. url: https://www.ncbi.nlm.nih.gov/pubmed/31849847/ doi: 10.3389/fmicb.2019.02541 id: cord-260834-v254de8k author: Lim, Chia Chiu title: Development of a Phage Display Panning Strategy Utilizing Crude Antigens: Isolation of MERS-CoV Nucleoprotein human antibodies date: 2019-04-15 words: 8295 sentences: 456 pages: flesch: 52 cache: ./cache/cord-260834-v254de8k.txt txt: ./txt/cord-260834-v254de8k.txt summary: The phage ELISA was conducted to measure the performances and effects of different blocking agents on the binding of αUbi phages against crude rUbi. Out of the four samples, the combination of PTM buffer and lysate showed the highest signal (1.226) detected with anti-c-myc-HRP as shown in Fig. 4c . Lysate preblocking and phage preincubation effects towards αUbi and M13KO7 phages against rUbi. To further optimize the biopanning conditions against crude antigens, the ''Yin-Yang'' (capture and eliminate) approach was designed to reduce non-specific binding by background phages. coli proteins in the crude fraction of rUbi with the actual concentration of rUbi being expected to be lower than the purified rUbi, the binding capability of αUbi is still unaffected as shown in phage ELISA assay upon affinity selection against crude rUbi. The blocking effect of PTM and E. abstract: Antibody phage display has been pivotal in the quest to generate human monoclonal antibodies for biomedical and research applications. Target antigen preparation is a main bottleneck associated with the panning process. This includes production complexity, downstream purification, quality and yield. In many instances, purified antigens are preferred for panning but this may not be possible for certain difficult target antigens. Here, we describe an improved procedure of affinity selection against crude or non-purified antigen by saturation of non-binders with blocking agents to promote positive binder enrichment termed as Yin-Yang panning. A naïve human scFv library with kappa light chain repertoire with a library size of 10(9) was developed. The improved Yin-Yang biopanning process was able to enrich monoclonal antibodies specific to the MERS-CoV nucleoprotein. Three unique monoclonal antibodies were isolated in the process. The Yin-Yang biopanning method highlights the possibility of utilizing crude antigens for the isolation of monoclonal antibodies by phage display. url: https://www.ncbi.nlm.nih.gov/pubmed/30988390/ doi: 10.1038/s41598-019-42628-6 id: cord-351498-bmq6zcb0 author: Martínez-Sernández, Victoria title: Comparison of recombinant cathepsins L1, L2, and L5 as ELISA targets for serodiagnosis of bovine and ovine fascioliasis date: 2018-03-21 words: 8277 sentences: 401 pages: flesch: 48 cache: ./cache/cord-351498-bmq6zcb0.txt txt: ./txt/cord-351498-bmq6zcb0.txt summary: In the present study, we developed and tested three indirect ELISAs using rFhpCL1, rFhpCL2, and rFhpCL5 and evaluated their recognition by sera from sheep and cattle naturally infected with F. In the present study, we developed and tested indirect ELISAs based on recombinant procathepsin L1 (rFhpCL1), rFhpCL2, or rFhpCL5, in order to investigate which of these targets are best recognized by sera from sheep and cattle naturally infected with F. Finally, the r values obtained on comparing the four ELISA methods for Fasciola-infected cattle and sheep sera are shown in Table 3 . These results suggest that the use of a single recombinant cathepsin/ procathepsin as target antigen in ELISAs for serodiagnosis of fascioliasis may limit the sensitivity of the assay when testing sera from some species, particularly cattle. (2001) who tested sera from sheep and cattle harboring other parasites, mainly nematodes, suggesting that the cross-reactivity may be due to common epitopes between recombinant Fasciola cathepsins and antigens present in other parasites. abstract: Infections caused by Fasciola hepatica are of great importance in the veterinary field, as they cause important economic losses to livestock producers. Serodiagnostic methods, typically ELISA (with either native or recombinant antigens), are often used for early diagnosis. The use of native antigens, as in the MM3-SERO ELISA (commercialized as BIO K 211, BIO-X Diagnostics), continues to be beneficial in terms of sensitivity and specificity; however, there is interest in developing ELISA tests based on recombinant antigens to avoid the need to culture parasites. Of the antigens secreted by adult flukes, recombinant procathepsin L1 (rFhpCL1) is the most commonly tested in ELISA to date. However, although adult flukes produce three different clades of CLs (FhCL1, FhCL2, and FhCL5), to our knowledge, the diagnostic value of recombinant FhCL2 and FhCL5 has not yet been investigated. In the present study, we developed and tested three indirect ELISAs using rFhpCL1, rFhpCL2, and rFhpCL5 and evaluated their recognition by sera from sheep and cattle naturally infected with F. hepatica. Although the overall antibody response to these three rFhpCLs was similar, some animals displayed preferential recognition for particular rFhpCLs. Moreover, for cattle sera, the highest sensitivity was obtained using rFhpCL2 (97%), being equal for both rFhpCL1 and rFhpCL5 (87.9%), after adjusting cut-offs for maximum specificity. By contrast, for sheep sera, the sensitivity was 100% for the three rFhpCLs. Finally, the presence of truncated and/or partially unfolded molecules in antigen preparations is postulated as a possible source of cross-reactivity. url: https://www.ncbi.nlm.nih.gov/pubmed/29564626/ doi: 10.1007/s00436-018-5809-7 id: cord-276732-u2d1z4ip author: Mauri, Tommaso title: Intraperitoneal adoptive transfer of mesenchymal stem cells enhances recovery from acid aspiration acute lung injury in mice date: 2017-03-06 words: 4445 sentences: 210 pages: flesch: 47 cache: ./cache/cord-276732-u2d1z4ip.txt txt: ./txt/cord-276732-u2d1z4ip.txt summary: -Arterial blood gas analysis for gas exchange -Wet-to-dry ratio as index of edema -Micro-CT scan to measure change over time in non-aerated lung tissue expressed as percentage of the whole lung tissue, with more negative values representing larger decrease of alveolar collapse; -Histopathology examination performed according to previous study [12] evaluating alveolar serofibrinous exudate and alveolar hemorrhage -Bronchoalveolar lavage for differential cell count, total protein content (with bicinchoninic acid method) and keratinocyte chemoattractant (CXCL1, previously named KC), and tumor necrosis factor-α (TNF-α) were assayed by ELISA -Blood withdrawal for PTX3 levels measurement in plasma (ELISA assay) (b)In 1 week from lung injury D-dimer (marker of fibrinolysis) [20] and matrix metalloproteinase 13 (MMP13), an enzyme that participates in collagen degradation [21] , were detected by ELISA and by western blot in lungs lysate, respectively. abstract: BACKGROUND: Mesenchymal stem cells (MSCs) might act as fine-tuners of inflammation during acute lung injury. We assessed the effects of adoptive transfer of MSCs in acid aspiration acute lung injury and explored the role of long pentraxin PTX3. METHODS: We conducted a prospective experimental interventional study on wild-type (WT) and PTX3-deficient (PTX3(−/−)) mice. Acute lung injury was induced in WT and PTX3(−/−) mice by instillation of hydrochloric acid into the right bronchus. One hour later, animals received intraperitoneal sterile phosphate-buffered saline (PBS), WT-MSCs (1 × 10(6)) or PTX3(−/−)-MSCs (1 × 10(6)). Twenty-four hours after injury, we measured the effects of treatments on arterial blood gases, wet/dry lung weight (W/D), CT scan analysis of lung collapse, neutrophils, TNFα and CXCL1 in bronchoalveolar lavage, and plasma PTX3. d-dimer was assayed in 1 week and OH-proline in 2 weeks to track the fibrotic evolution. RESULTS: In 24 h, in comparison to PBS, WT-MSCs improved oxygenation and reduced W/D and alveolar collapse. These effects were associated with decreased concentrations of alveolar neutrophils and cytokines. WT-MSCs increased d-dimer concentration and decreased OH-proline levels, too. Treatment with PTX3(−/−)-MSCs ameliorated oxygenation, W/D, and alveolar TNFα, though to a lesser extent than WT-MSCs. PTX3(−/−)-MSCs did not improve lung collapse, neutrophil count, CXCL1, d-dimer, and OH-proline concentrations. The protective effects of WT-MSCs were dampened by lack of endogenous PTX3, too. CONCLUSIONS: In acid aspiration acute lung injury, MSCs improve pulmonary function and limit fibrosis by fine-tuning inflammation. The role of PTX3 in determining MSCs’ effects might merit further scrutiny. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40635-017-0126-5) contains supplementary material, which is available to authorized users. url: https://doi.org/10.1186/s40635-017-0126-5 doi: 10.1186/s40635-017-0126-5 id: cord-292862-ezrkg0dc author: Myerson, Jacob W. title: Supramolecular Organization Predicts Protein Nanoparticle Delivery to Neutrophils for Acute Lung Inflammation Diagnosis and Treatment date: 2020-04-18 words: 14275 sentences: 744 pages: flesch: 46 cache: ./cache/cord-292862-ezrkg0dc.txt txt: ./txt/cord-292862-ezrkg0dc.txt summary: We show that polystyrene nanoparticles and five liposome formulations do not accumulate in injured lungs, indicating that nanostructures that are not based on protein are not intrinsically drawn to marginated neutrophils in acute inflammation. 6, 10, 14, 18 Single cell suspensions prepared from mouse lungs were probed by flow cytometry to further characterize pulmonary neutrophils in naïve mice and in mice following LPS-induced inflammation. The protein component of each particle was labeled with 125 I for tracing in biodistributions, and assessed 30 minutes after IV administration of NPs. Both absolute LDNG lung uptake and ratio of lung uptake to liver uptake registered a ~25-fold increase between naïve control and LPS-injured animals (Figure 2A , Supplementary Table 1) . As with LDNGs and albumin NPs in Figure 2C -H, single cell suspensions were prepared from LPS-inflamed and naïve control lungs after circulation of fluorescent DBCO-IgG liposomes. abstract: Acute lung inflammation has severe morbidity, as seen in COVID-19 patients. Lung inflammation is accompanied or led by massive accumulation of neutrophils in pulmonary capillaries (“margination”). We sought to identify nanostructural properties that predispose nanoparticles to accumulate in pulmonary marginated neutrophils, and therefore to target severely inflamed lungs. We designed a library of nanoparticles and conducted an in vivo screen of biodistributions in naive mice and mice treated with lipopolysaccharides. We found that supramolecular organization of protein in nanoparticles predicts uptake in inflamed lungs. Specifically, nanoparticles with agglutinated protein (NAPs) efficiently home to pulmonary neutrophils, while protein nanoparticles with symmetric structure (e.g. viral capsids) are ignored by pulmonary neutrophils. We validated this finding by engineering protein-conjugated liposomes that recapitulate NAP targeting to neutrophils in inflamed lungs. We show that NAPs can diagnose acute lung injury in SPECT imaging and that NAP-like liposomes can mitigate neutrophil extravasation and pulmonary edema arising in lung inflammation. Finally, we demonstrate that ischemic ex vivo human lungs selectively take up NAPs, illustrating translational potential. This work demonstrates that structure-dependent interactions with neutrophils can dramatically alter the biodistribution of nanoparticles, and NAPs have significant potential in detecting and treating respiratory conditions arising from injury or infections. url: https://doi.org/10.1101/2020.04.15.037564 doi: 10.1101/2020.04.15.037564 id: cord-335591-r0x8yaqj author: Ohnishi, Kazuo title: Establishment and Characterization of Monoclonal Antibodies Against SARS Coronavirus date: 2007-11-28 words: 3126 sentences: 242 pages: flesch: 67 cache: ./cache/cord-335591-r0x8yaqj.txt txt: ./txt/cord-335591-r0x8yaqj.txt summary: The hybridomas produce monoclonal antibodies that recognize viral component molecules, including the spike protein (S) and the nucleocapsid protein (N), enabling the immunological detection of SARS-CoV by immunofluorescence staining, immunoblot, or an antigen-capture ELISA system. Based on clinical experience, several options have been considered in the quest to develop the capacity to accurately diagnose SARS-CoV infection, including molecular biology techniques and serological tests such as antigen-capture ELISA assay and immunofluorescence assay to detect virus-infected cells in respiratory swabs (3-7) . These mAbs enable the general immunological detection of SARS-CoV by methods such as immunofluorescent staining, immunoblotting, and immunohistology, in addition to the construction of a highly sensitive antigen-capture sandwich ELISA (6). The UV-inactivated purified SARS-CoV samples (see Note 1), which are serially diluted with 1% OVA/PBS-Tween, are added to the wells and incubated for 1 h at room temperature abstract: Immunological detection of viruses and their components by monoclonal antibodies is a powerful method for studying the structure and function of viral molecules. Here we describe detailed methods for establishing monoclonal antibodies against severe acute respiratory syndrome coronavirus (SARS-CoV). B cell hybridomas are generated from mice that are hyperimmunized with inactivated SARS-CoV virions. The hybridomas produce monoclonal antibodies that recognize viral component molecules, including the spike protein (S) and the nucleocapsid protein (N), enabling the immunological detection of SARS-CoV by immunofluorescence staining, immunoblot, or an antigen-capture ELISA system. In addition, several S protein-specific antibodies are shown to have in vitro neutralization activity. Thus the monoclonal antibody approach provides useful tools for rapid and specific diagnosis of SARS, as well as for possible antibody-based treatment of the disease. url: https://doi.org/10.1007/978-1-59745-181-9_15 doi: 10.1007/978-1-59745-181-9_15 id: cord-009800-tajkpgkj author: Orellana, Mhica V. title: An immunoprobe to measure Rubisco concentrations and maximal photosynthetic rates of individual phytoplankton cells date: 2003-12-22 words: 5874 sentences: 306 pages: flesch: 42 cache: ./cache/cord-009800-tajkpgkj.txt txt: ./txt/cord-009800-tajkpgkj.txt summary: The cross‐reactivity of an immunological probe to the key photosynthetic enzyme Rubisco (ribulose‐1,5‐bisphosphate carboxylase/oxygenase) was characterized as part of a larger effort to determine maximal photosynthetic rates of individual phytoplankton cells. In order to use an immunoprobe to quantitatively measure Rubisco concentration within individual cells in a mixed-species assemblage, it is imperative to determine: first, whether the probe is truly specific to only the large subunit of Rubisco; second, whether the probe binds to the Rubisco large subunit of all phytoplankton species with equal affinity; and third, whether immunologically determined concentrations of Rubisco are well correlated with maximal photosynthetic rates. The results indicate that an affinity-purified anti-Rubisco probe can be used to quantify Rubisco concentrations and maximal photosynthetic potential of individual phytoplankton cells in mixed-species assemblages. When the more quantitative dot blot assays were used with purified Rubisco from different species, a high degree of variability in the binding affinity with the polyclonal antiserum was evident (Fig. 1) . abstract: The cross‐reactivity of an immunological probe to the key photosynthetic enzyme Rubisco (ribulose‐1,5‐bisphosphate carboxylase/oxygenase) was characterized as part of a larger effort to determine maximal photosynthetic rates of individual phytoplankton cells. Polyclonal antiserum was produced against purified Rubisco from the marine diatom Chaetoceros gracilis. The results of western immunoblotting demonstrated that the antiserum reacted positively with Rubisco from 38 species of algae and higher plants and failed to react with only three species of dinoflagellates and one prochlorophyte species. However, the binding affinity or the strength of the cross‐reaction for the polyclonal antiserum with purified Rubisco varied among species. The antiserum was then affinity purified against spinach Rubisco and its binding affinity for purified Rubisco determined by ELISA. Two taxonomic groupings resulted: one with high‐binding affinity (these species included chrysophytes, bacillariophytes, prymnesiophytes, and chlorophytes) and the other with low‐binding affinity (dinophytes and cyanophytes). Rubisco concentration per cell and light‐saturated rates of photosynthesis were highly correlated for cultures of the diatom Thalassiosira weissflogii. These results indicate that affinity‐purified antiserum can be rigorously characterized for use in quantifying Rubisco concentration and for assessing the maximal photosynthetic potential of individual phytoplankton cells. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7165624/ doi: 10.4319/lo.1992.37.3.0478 id: cord-274396-l611eisi author: Park, Su-Jin title: Antiviral Efficacies of FDA-Approved Drugs against SARS-CoV-2 Infection in Ferrets date: 2020-05-22 words: 4355 sentences: 208 pages: flesch: 46 cache: ./cache/cord-274396-l611eisi.txt txt: ./txt/cord-274396-l611eisi.txt summary: While the lopinavir-ritonavir-, hydroxychloroquine sulfate-, or emtricitabine-tenofovir-treated group exhibited lower overall clinical scores than the phosphate-buffered saline (PBS)-treated control group, the virus titers in nasal washes, stool specimens, and respiratory tissues were similar between all three antiviral-candidate-treated groups and the PBS-treated control group. Compared to the PBS-treated control group, azathioprine-immunosuppressed ferrets exhibited a longer period of clinical illness, higher virus titers in nasal turbinate, delayed virus clearance, and significantly lower serum neutralization (SN) antibody titers. In order to determine the antiviral efficacies of lopinavir-ritonavir, hydroxychloroquine (HCQ) sulfate, or emtricitabine-tenofovir for treatment of SARS-CoV-2 infection, SARS-CoV-2 antibody-free ferrets (10/group) were inoculated with 10 5.8 50% tissue culture infective doses (TCID 50 )/ml of an NMC-nCoV02 strain through the intranasal (i.n.) route ( Fig. 1 ). Therefore, although clinical symptoms were attenuated in ferret groups treated with antiviral candidates, we also evaluated virus titers in respiratory and gastrointestinal tracts using nasal washes and stool samples, respectively, from SARS-CoV-2-infected ferrets. abstract: Due to the urgent need of a therapeutic treatment for coronavirus (CoV) disease 2019 (COVID-19) patients, a number of FDA-approved/repurposed drugs have been suggested as antiviral candidates at clinics, without sufficient information. Furthermore, there have been extensive debates over antiviral candidates for their effectiveness and safety against severe acute respiratory syndrome CoV 2 (SARS-CoV-2), suggesting that rapid preclinical animal studies are required to identify potential antiviral candidates for human trials. To this end, the antiviral efficacies of lopinavir-ritonavir, hydroxychloroquine sulfate, and emtricitabine-tenofovir for SARS-CoV-2 infection were assessed in the ferret infection model. While the lopinavir-ritonavir-, hydroxychloroquine sulfate-, or emtricitabine-tenofovir-treated group exhibited lower overall clinical scores than the phosphate-buffered saline (PBS)-treated control group, the virus titers in nasal washes, stool specimens, and respiratory tissues were similar between all three antiviral-candidate-treated groups and the PBS-treated control group. Only the emtricitabine-tenofovir-treated group showed lower virus titers in nasal washes at 8 days postinfection (dpi) than the PBS-treated control group. To further explore the effect of immune suppression on viral infection and clinical outcome, ferrets were treated with azathioprine, an immunosuppressive drug. Compared to the PBS-treated control group, azathioprine-immunosuppressed ferrets exhibited a longer period of clinical illness, higher virus titers in nasal turbinate, delayed virus clearance, and significantly lower serum neutralization (SN) antibody titers. Taken together, all antiviral drugs tested marginally reduced the overall clinical scores of infected ferrets but did not significantly affect in vivo virus titers. Despite the potential discrepancy of drug efficacies between animals and humans, these preclinical ferret data should be highly informative to future therapeutic treatment of COVID-19 patients. url: https://www.ncbi.nlm.nih.gov/pubmed/32444382/ doi: 10.1128/mbio.01114-20 id: cord-295033-5fd9bu60 author: Parma, Y.R. title: Antibodies anti-Shiga toxin 2 B subunit from chicken egg yolk: Isolation, purification and neutralization efficacy date: 2011-09-15 words: 6045 sentences: 326 pages: flesch: 53 cache: ./cache/cord-295033-5fd9bu60.txt txt: ./txt/cord-295033-5fd9bu60.txt summary: The data suggest that immunization of hens with Stx2B could be a strategy to obtain at low cost a relatively high concentration of anti-Stx2 egg yolk IgY, able to neutralize Stx2 lethal activity. The data suggest that immunization of hens with Stx2B could be a strategy to obtain at low cost a relatively high concentration of anti-Stx2 egg yolk IgY, able to neutralize Stx2 lethal activity. Specific anti-Stx2B polyclonal antibodies obtained from chicken egg yolk and rabbit sera recognized not only the denatured and native form of B subunit, used for immunization but the antibodies were also able to recognize the denatured and native wild type Stx2 holotoxin in western blot (Fig. 3) , indirect ELISA (Fig. 4) and sandwich ELISA (Fig. 5) . In the present report, specific egg yolk IgY antibodies with binding and neutralizing capabilities against the wild type Stx2 toxin were obtained after immunization of laying hens. abstract: Shiga toxins (Stx1 and Stx2) are the main virulence factors of enterohemorrhagic Escherichia coli (EHEC), a foodborne pathogen associated with diarrhea, hemorrhagic colitis and hemolytic uremic syndrome. The aim of this study was to evaluate the antibodies against Stx2 obtained from egg yolks of laying hens immunized with a recombinant Stx2B subunit. A high specific response in serum was observed 25 days after the first immunization and IgY antibodies were extracted from day 47th and purified from egg yolk. A concentration of 0.84 mg of total IgY/ml of egg yolk was obtained, of which 8% were antigen specific. The ability of anti-Stx2B IgY to recognize Stx2B and Stx2 either in solid-phase or in solution were evaluated and compared with anti-Stx2B rabbit antibodies by Western blotting and ELISA. The protective efficacy of IgY against Stx2 was determined by in vitro and in vivo experiments. The results show that IgY was able to recognize Stx2B and Stx2 in denatured conditions, attached to a solid-phase and free in solution. The anti-Stx2B IgY could effectively block the biological activity of Stx2 on Vero cells and protect mice from Stx2 challenge. The data suggest that immunization of hens with Stx2B could be a strategy to obtain at low cost a relatively high concentration of anti-Stx2 egg yolk IgY, able to neutralize Stx2 lethal activity. IgY technology could be an useful tool for research, diagnosis and therapy of EHEC infection. url: https://www.sciencedirect.com/science/article/pii/S0041010111002273 doi: 10.1016/j.toxicon.2011.07.009 id: cord-026866-0hlre9i6 author: Perruzza, Lisa title: Prophylactic Activity of Orally Administered FliD-Reactive Monoclonal SIgA Against Campylobacter Infection date: 2020-06-09 words: 9357 sentences: 371 pages: flesch: 38 cache: ./cache/cord-026866-0hlre9i6.txt txt: ./txt/cord-026866-0hlre9i6.txt summary: In this study, we describe the prophylactic activity of orally delivered recombinant SIgA generated from two human monoclonal antibodies (CAA1 and CCG4) isolated for their reactivity against the flagellar-capping protein FliD, which is essential for bacteria motility and highly conserved across Campylobacter species associated with severe enteritis. In this study, we describe the prophylactic activity of orally delivered recombinant SIgA generated from two human monoclonal antibodies (CAA1 and CCG4) isolated for their reactivity against the flagellar-capping protein FliD, which is essential for bacteria motility and highly conserved across Campylobacter species associated with severe enteritis. In this study, an immunocompetent mouse model of Campylobacter infection was used to evaluated the prophylactic activity of orally delivered recombinant SIgA generated from human monoclonal antibodies isolated and selected for their reactivity against the flagellar-capping protein FliD, which is pivotal for bacteria motility (25), and highly conserved across Campylobacter species frequently associated with severe neonatal enteritis (26) . abstract: Campylobacter infection is one of the most common causes of bacterial gastroenteritis worldwide and a major global health threat due to the rapid development of antibiotic resistance. Currently, there are no vaccines approved to prevent campylobacteriosis, and rehydration is the main form of therapy. Secretory immunoglobulin A (SIgA) is the main antibody class found in mucous secretions, including human milk, and serves as the first line of defense for the gastrointestinal epithelium against enteric pathogens. In this study, we describe the prophylactic activity of orally delivered recombinant SIgA generated from two human monoclonal antibodies (CAA1 and CCG4) isolated for their reactivity against the flagellar-capping protein FliD, which is essential for bacteria motility and highly conserved across Campylobacter species associated with severe enteritis. In an immunocompetent weaned mouse model, a single oral administration of FliD-reactive SIgA CAA1 or CCG4 at 2 h before infection significantly enhances Campylobacter clearance at early stages post-infection, reducing the levels of inflammation markers associated with epithelial damage and polymorphonuclear (PMN) cells infiltration in the cecum lamina propria. Our data indicate that the prophylactic activity of CAA1 and CCG4 is not only dependent on the specificity to FliD but also on the use of the SIgA format, as the immunoglobulin G (IgG) versions of the same antibodies did not confer a comparable protective effect. Our work emphasizes the potential of FliD as a target for the development of vaccines and supports the concept that orally administered FliD-reactive SIgA can be developed to prevent or mitigate the severity of Campylobacter infections as well as the development of post-infection syndromes. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296071/ doi: 10.3389/fimmu.2020.01011 id: cord-003915-kje8lvgl author: Pigeyre, Laetitia title: Interaction of a Densovirus with Glycans of the Peritrophic Matrix Mediates Oral Infection of the Lepidopteran Pest Spodoptera frugiperda date: 2019-09-17 words: 9040 sentences: 462 pages: flesch: 47 cache: ./cache/cord-003915-kje8lvgl.txt txt: ./txt/cord-003915-kje8lvgl.txt summary: As orally transmitted viruses, densoviruses, are also challenged by the complexity of the insect gut barriers, more specifically by the chitinous peritrophic matrix, that lines and protects the midgut epithelium; how capsids stick to and cross these barriers to reach their final cell destination where replication goes has been poorly studied in insects. In addition, we showed that JcDV early infection results in (i) an arrest of N-Acetylglucosamine (GlcNAc) secretion by epithelial cells associated with a disorganization of the PM structure mimicking the effect of chitin-binding plant lectin; (ii) substantial changes in the expression of gut genes, which may also contribute to an early gut dysfunction and participate to viral pathogenesis. Results presented here show that JcDV capsids display carbohydrate-binding properties that insure recognition of the peritrophic matrix and determines caterpillars oral infection. abstract: The success of oral infection by viruses depends on their capacity to overcome the gut epithelial barrier of their host to crossing over apical, mucous extracellular matrices. As orally transmitted viruses, densoviruses, are also challenged by the complexity of the insect gut barriers, more specifically by the chitinous peritrophic matrix, that lines and protects the midgut epithelium; how capsids stick to and cross these barriers to reach their final cell destination where replication goes has been poorly studied in insects. Here, we analyzed the early interaction of the Junonia coenia densovirus (JcDV) with the midgut barriers of caterpillars from the pest Spodoptera frugiperda. Using combination of imaging, biochemical, proteomic and transcriptomic analyses, we examined in vitro, ex vivo and in vivo the early interaction of the capsids with the peritrophic matrix and the consequence of early oral infection on the overall gut function. We show that the JcDV particle rapidly adheres to the peritrophic matrix through interaction with different glycans including chitin and glycoproteins, and that these interactions are necessary for oral infection. Proteomic analyses of JcDV binding proteins of the peritrophic matrix revealed mucins and non-mucins proteins including enzymes already known to act as receptors for several insect pathogens. In addition, we show that JcDV early infection results in an arrest of N-Acetylglucosamine secretion and a disruption in the integrity of the peritrophic matrix, which may help viral particles to pass through. Finally, JcDV early infection induces changes in midgut genes expression favoring an increased metabolism including an increased translational activity. These dysregulations probably participate to the overall dysfunction of the gut barrier in the early steps of viral pathogenesis. A better understanding of early steps of densovirus infection process is crucial to build biocontrol strategies against major insect pests. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783882/ doi: 10.3390/v11090870 id: cord-265740-wjdeps3h author: Radbel, Jared title: Detection of SARS-CoV-2 is comparable in clinical samples preserved in saline or viral transport media date: 2020-05-13 words: 2250 sentences: 121 pages: flesch: 51 cache: ./cache/cord-265740-wjdeps3h.txt txt: ./txt/cord-265740-wjdeps3h.txt summary: Given that SARS-CoV-2 viral RNA has demonstrated stability, we posited that phosphate buffered saline (PBS) may be a viable transport medium, as an alternative to VTM), for clinical qPCR testing. We assessed the intraand inter-individual reliability of SARS-CoV-2 qPCR in clinical endotracheal secretion samples transported in VTM or PBS, evaluating the stability of the RT-qPCR signal for three viral targets (N gene, ORF1ab, and S gene) when samples were stored in these media at room temperature for up to 18 hours. We report that using PBS as a transport medium has high intra-and inter-individual reliability, maintains viral stability, and is comparable to VTM in the detection of the three SARS-CoV-2 genes through 18 hours of storage. SARS-CoV-2 detection using standard testing of upper airway secretions requires a nasopharyngeal (NP) or oropharyngeal (OP) swab that is transported to a clinical laboratory using viral transport media (VTM) (https://www.fda.gov/medical-devices/emergency-situations-medical-devices/faqs-diagnostic-testingsars-cov-2#offeringtests, last accessed April 29 2020). abstract: As the COVID-19 pandemic sweeps across the world, the availability of viral transport media (VTM) has become severely limited, contributing to delays in diagnosis and rationing of diagnostic testing. Given that SARS-CoV-2 viral RNA has demonstrated stability, we posited that phosphate buffered saline (PBS) may be a viable transport medium, as an alternative to VTM), for clinical qPCR testing. We assessed the intra- and inter-individual reliability of SARS-CoV-2 qPCR in clinical endotracheal secretion samples transported in VTM or PBS, evaluating the stability of the RT-qPCR signal for three viral targets (N gene, ORF1ab, and S gene) when samples were stored in these media at room temperature for up to 18 hours. We report that using PBS as a transport medium has high intra-and inter-individual reliability, maintains viral stability, and is comparable to VTM in the detection of the three SARS-CoV-2 genes through 18 hours of storage. Our study establishes PBS as a clinically useful medium that can be readily deployed for transporting and short-term preservation of specimens containing SARS-CoV-2. Use of PBS as a transport medium has the potential to increase testing capacity for SARS-CoV-2, aiding more widespread screening and early diagnosis of COVID-19. url: https://www.sciencedirect.com/science/article/pii/S1525157820303238?v=s5 doi: 10.1016/j.jmoldx.2020.04.209 id: cord-001732-4eyn7pjq author: Riede, O title: Preclinical safety and tolerability of a repeatedly administered human leishmaniasis DNA vaccine date: 2015-04-30 words: 6339 sentences: 336 pages: flesch: 49 cache: ./cache/cord-001732-4eyn7pjq.txt txt: ./txt/cord-001732-4eyn7pjq.txt summary: Evaluation of single-dose and repeated-dose toxicity of the vaccine candidate after i.d. administration to naive, non-infected mice did not reveal any safety concerns. To assess toxicity of LEISHDNAVAX in naive mice, sterile phosphate-buffered saline (PBS, placebo) and ascending doses of the vaccine were injected either once or five times in weekly intervals (Table 1) . Twenty-four hour after single or repeated injection, MIDGE-Th1 vector DNA was detected in almost all organs and tissues examined, suggesting that it was distributed systemically, most likely via the lymphatic system and the blood stream. Groups of 10 BALB/c mice (5 male, 5 female) were immunized i.d. at the tail base five times in weekly intervals with either PBS or LEISHDNAVAX (10, 50 or 100 μg per dose). In summary, we have shown here that LEISHDNAVAX, a novel DNA vaccine candidate against leishmaniasis is safe and well tolerated in both naive and Leishmania-infected mice. abstract: The leishmaniases are a complex of vector-borne diseases caused by protozoan parasites of the genus Leishmania. LEISHDNAVAX is a multi-antigen, T-cell epitope-enriched DNA vaccine candidate against human leishmaniasis. The vaccine candidate has been proven immunogenic and showed prophylactic efficacy in preclinical studies. Here, we describe the safety testing of LEISHDNAVAX in naive mice and rats, complemented by the demonstration of tolerability in Leishmania-infected mice. Biodistribution and persistence were examined following single and repeated intradermal (i.d.) administration to rats. DNA vectors were distributed systemically but did not accumulate upon repeated injections. Although vector DNA was cleared from most other tissues within 60 days after the last injection, it persisted in skin at the site of injection and in draining lymph nodes. Evaluation of single-dose and repeated-dose toxicity of the vaccine candidate after i.d. administration to naive, non-infected mice did not reveal any safety concerns. LEISHDNAVAX was also well tolerated in Leishmania-infected mice. Taken together, our results substantiate a favorable safety profile of LEISHDNAVAX in both naive and infected animals and thus, support the initiation of clinical trials for both preventive and therapeutic applications of the vaccine. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530203/ doi: 10.1038/gt.2015.35 id: cord-305648-majanu8l author: Schountz, Tony title: Rapid Field Immunoassay for Detecting Antibody to Sin Nombre Virus in Deer Mice date: 2007-10-17 words: 1633 sentences: 96 pages: flesch: 57 cache: ./cache/cord-305648-majanu8l.txt txt: ./txt/cord-305648-majanu8l.txt summary: We developed a 1-hour field enzyme immunoassay (EIA) for detecting antibody to Sin Nombre virus in deer mice (Peromyscus maniculatus). Samples were retested under laboratory conditions with PAGEIA and standard Centers for Disease Control and Prevention (CDC) enzyme immunoassay (EIA) (5) . One sample (HA-2564) was scored negative by fi eld and laboratory PAGEIA, but (low) positive (optical density [OD] of 0.327) by conventional EIA (Table) . One sample (TS-0830-7) scored as 1+ in the fi eld was determined to be negative on subsequent laboratory testing by both PAGEIA and conventional EIA. The other 4 samples (HB-2628, HA-2609, HA-2616, HB-2710) were scored as positive by fi eld and laboratory PAGEIA but negative by conventional EIA. Similar laboratorybased PAGEIAs have also been used to detect antibody to antigens of agents causing other infectious diseases, including severe acute respiratory syndrome coronavirus-like viruses and Nipah virus in bats (13) (14) (15) . abstract: We developed a 1-hour field enzyme immunoassay (EIA) for detecting antibody to Sin Nombre virus in deer mice (Peromyscus maniculatus). The assay specificity and sensitivity were comparable to those of a standard EIA. This test will permit identification of rodents with antibody to this and perhaps other hantaviruses. url: https://www.ncbi.nlm.nih.gov/pubmed/18258020/ doi: 10.3201/eid1310.070383 id: cord-309742-fd1qmr87 author: Slepushkin, Vladimir A. title: Infection of Human Airway Epithelia with H1N1, H2N2, and H3N2 Influenza A Virus Strains date: 2016-12-14 words: 5526 sentences: 311 pages: flesch: 48 cache: ./cache/cord-309742-fd1qmr87.txt txt: ./txt/cord-309742-fd1qmr87.txt summary: Therefore, we assayed A/PR/8/34 (H1N1), A/Japan/305/57 (H2N2), and X31 (H3N2) influenza virus strains for binding and infection on fully differentiated primary cultures of airway epithelia isolated from human bronchus, grown on semiporous filters at an air–liquid interface. These data show that influenza viruses with SAα2,3Gal binding specificity, like Japan, productively infect differentiated human airway epithelia from the apical surface. For measurement of the kinetics of influenza virus production from infected airway cells in one infectious cycle, 100 l of the virus preparation was diluted in Dulbecco''s PBS (Life Technologies, Inc., Grand Island, NY) and applied to the apical surface of the epithelia (m.o.i. of 0.1). To infect airway epithelia with different influenza virus strains from the basolateral side, the Millicell culture insert was turned over and virus preparations diluted in PBS were applied in a 100-l volume to the bottom of the membrane (m.o.i. ϭ 0.1). abstract: Three subtypes of influenza A virus cause human disease: H1N1, H2N2, and H3N2. Although all result in respiratory illness, little is known about how these subtypes infect differentiated airway epithelia. Therefore, we assayed A/PR/8/34 (H1N1), A/Japan/305/57 (H2N2), and X31 (H3N2) influenza virus strains for binding and infection on fully differentiated primary cultures of airway epithelia isolated from human bronchus, grown on semiporous filters at an air–liquid interface. In this model system, viral infectivity was highest when virus was applied to the apical versus the basolateral surface; Japan was most infectious, followed by PR8. The X31 strain showed very low levels of infectivity. Confocal microscopy and fluorescence-resonance energy transfer studies indicated that Japan virus could enter and fuse with cellular membranes, while infection with X31 virions was greatly inhibited. Japan virus could also productively infect human trachea explant tissues. These data show that influenza viruses with SAα2,3Gal binding specificity, like Japan, productively infect differentiated human airway epithelia from the apical surface. These data are important to consider in the development of pseudotyped recombinant viral vectors for gene transfer to human airway epithelia for gene therapy. url: https://www.ncbi.nlm.nih.gov/pubmed/11273782/ doi: 10.1006/mthe.2001.0277 id: cord-334165-7gfk554m author: Stadlbauer, Daniel title: SARS‐CoV‐2 Seroconversion in Humans: A Detailed Protocol for a Serological Assay, Antigen Production, and Test Setup date: 2020-04-17 words: 5286 sentences: 414 pages: flesch: 69 cache: ./cache/cord-334165-7gfk554m.txt txt: ./txt/cord-334165-7gfk554m.txt summary: Basic Protocol 1: Mammalian cell transfection and protein purification Basic Protocol 2: A two‐stage ELISA for high‐throughput screening of human serum samples for antibodies binding to the spike protein of SARS‐CoV‐2 We reported in our earlier work that individuals not exposed to SARS-CoV-2 are completely naïve to the spike protein, and their serum samples show little or no reactivity in an ELISA (Amanat et al., 2020) . We developed this as a two-stage ELISA in which the first stage (''a'' steps below) includes relatively high-throughput screening of samples in a single serum dilution against the RBD (which expresses very well and therefore can be produced in greater quantities). This is followed by a second stage (''b'' steps below) in which positive samples from the first stage undergo a confirmatory ELISA against the full-length spike protein (which is harder to express; therefore there is usually less available). i. Thaw the required number of vials of antigen (SARS-CoV-2 RBD protein) to coat 96-well microtiter ELISA plates at a concentration of 2 μg/ml. abstract: In late 2019, cases of atypical pneumonia were detected in China. The etiological agent was quickly identified as a betacoronavirus (named SARS‐CoV‐2), which has since caused a pandemic. Several methods allowing for the specific detection of viral nucleic acids have been established, but these only allow detection of the virus during a short period of time, generally during acute infection. Serological assays are urgently needed to conduct serosurveys, to understand the antibody responses mounted in response to the virus, and to identify individuals who are potentially immune to re‐infection. Here we describe a detailed protocol for expression of antigens derived from the spike protein of SARS‐CoV‐2 that can serve as a substrate for immunological assays, as well as a two‐stage serological enzyme‐linked immunosorbent assay (ELISA). These assays can be used for research studies and for testing in clinical laboratories. © 2020 The Authors. Current Protocols in Microbiology published by Wiley Periodicals LLC. Basic Protocol 1: Mammalian cell transfection and protein purification Basic Protocol 2: A two‐stage ELISA for high‐throughput screening of human serum samples for antibodies binding to the spike protein of SARS‐CoV‐2 url: https://doi.org/10.1002/cpmc.100 doi: 10.1002/cpmc.100 id: cord-303381-xvzhb7ix author: TSURUTA, Yuya title: The requirement of environmental acidification for Ibaraki virus infection to host cells date: 2015-08-28 words: 1987 sentences: 121 pages: flesch: 49 cache: ./cache/cord-303381-xvzhb7ix.txt txt: ./txt/cord-303381-xvzhb7ix.txt summary: The effect of environmental acidification on Ibaraki virus (IBAV) infection was tested using endosomal inhibitory chemicals and low pH treatment. Treatment of target cells with endosomal inhibitors significantly decreased the progeny virus production. HmLu-1 (hamster lung) cells were infected with IBAV in the presence of three different endosome inhibitors, bafilomycin A1 (Baf A1, Sigma, St. Louis, MO, U.S.A.), chlorpromazine (CPZ, Abcam, Cambridge, U.K.) and dynasore (Wako, Osaka, Japan). These results indicated that IBAV utilizes clathrin-dependent endosomal pathway for infection and coincided with the previous research on bluetongue virus entry [8] . To confirm the effect of low pH on virus infectivity, purified IBAV was incubated in PBS (−) with several pH (pH=4, 7 or 9) for five min and infected to HmLu-1 at MOI=0.01. The result obtained above implicated that low pH treat-ment removes IBAV outer capsid proteins from the particle and initiates its infection. abstract: The effect of environmental acidification on Ibaraki virus (IBAV) infection was tested using endosomal inhibitory chemicals and low pH treatment. Treatment of target cells with endosomal inhibitors significantly decreased the progeny virus production. IBAV outer capsid proteins, VP5 and VP2, were removed from virion when purified IBAV was exposed to low pH environment. Further experiment showed that the exposure to low pH buffer facilitated IBAV infection when the cellular endosomal pathway was impaired by bafilomycin A1. Results obtained in this study suggest that acidic environment is essential to initiate IBAV infection. url: https://doi.org/10.1292/jvms.15-0222 doi: 10.1292/jvms.15-0222 id: cord-011106-h20vbmbo author: Takeda, Yohei title: Antiviral Activities of Hibiscus sabdariffa L. Tea Extract Against Human Influenza A Virus Rely Largely on Acidic pH but Partially on a Low-pH-Independent Mechanism date: 2019-10-16 words: 5362 sentences: 330 pages: flesch: 54 cache: ./cache/cord-011106-h20vbmbo.txt txt: ./txt/cord-011106-h20vbmbo.txt summary: Here, we analyzed the antiviral activity of hibiscus (Hibiscus sabdariffa L.) tea extract against human IAV and evaluated its potential as a novel anti-IAV drug and a safe inactivating agent for whole inactivated vaccine. In addition, we assessed hibiscus tea extract''s potential as a candidate for novel anti-IAV drug and as an inactivating agent for whole-virus vaccines. PR8 virus propagated in allantoic fluid was mixed with an equal amount of neutral and acidic pH PBS, Hib[crude], frHibis, or PCA. 50 μl PBS, formalin-, β-PL-, or acidic Hib[crude]-inactivated PR8 virus vaccine was intranasally administered in mice (first vaccination) under light anesthesia with isolflurane (Intervet K.K., Tokyo, Japan). The neutralized Hib[crude] in the blood loses potent anti-IAV activity due to acid, and the low-pH-independent antiviral activity is inadequate to inactivate virus in vivo. abstract: Influenza A virus (IAV) infection is perennially one of the leading causes of death worldwide. Effective therapy and vaccination are needed to control viral expansion. However, current anti-IAV drugs risk inducing drug-resistant virus emergence. Although intranasal administration of whole inactivated virus vaccine can induce efficient protective immunity, formalin and β-propiolactone are the currently used and harmful inactivating agents. Here, we analyzed the antiviral activity of hibiscus (Hibiscus sabdariffa L.) tea extract against human IAV and evaluated its potential as a novel anti-IAV drug and a safe inactivating agent for whole inactivated vaccine. The in vitro study revealed that the pH of hibiscus tea extract is acidic, and its rapid and potent antiviral activity relied largely on the acidic pH. Furthermore, the mouse study showed that the acidic extract was not effective for either therapeutic or vaccination purposes. However, hibiscus tea extract and protocatechuic acid, one of the major components of the extract, showed not only potent acid-dependent antiviral activity but also weak low-pH-independent activity. The low-pH-independent activity did not affect the conformation of immunodominant hemagglutinin protein. Although this low-pH-independent activity is very limited, it may be suitable for the application to medication and vaccination because this activity is not affected by the neutral blood environment and does not lose antigenicity of hemagglutinin. Further study of the low-pH-independent antiviral mechanism and attempts to enhance the antiviral activity may establish a novel anti-IAV therapy and vaccination strategy. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223586/ doi: 10.1007/s12560-019-09408-x id: cord-327568-5vo4nmei author: Tosini, Fabio title: Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection date: 2019-05-15 words: 7398 sentences: 362 pages: flesch: 52 cache: ./cache/cord-327568-5vo4nmei.txt txt: ./txt/cord-327568-5vo4nmei.txt summary: title: Delivery of SA35 and SA40 peptides in mice enhances humoral and cellular immune responses and confers protection against Cryptosporidium parvum infection parvum proteins, were tested for their ability to induce immune responses in adult mice and for protection on neonate BALB/c mice born from females immunised by mucosal delivery of both peptides. The IP immunisation of adult BALB/c mice to a single antigen (SA35 or SA40) or to a mixture of the two antigens (SA35/40 mix) induced specific anti-Cryptosporidium IgG in serum after day 14 following initial administration. The mucosal delivery of SA35/40 mix in female BALB/c mice induced specific anti-Cryptosporidium IgG (mainly IgG1) in serum 21 days after initial immunisation. In humans, maternal immunisation with tetanus toxoid has Fig. 9 Quantification of COWP gene DNA copies by qPCR in the intestinal content of neonate mice infected with 5 × 10 3 Cryptosporidium parvum oocysts. abstract: BACKGROUND: Cryptosporidium parvum is a major cause of diarrhea in children and ruminants at the earliest stages of life. Maternal antibodies represent the main shield of neonate mammals for most of the infections. Two recombinant antigens (SA35 and SA40), portions of two C. parvum proteins, were tested for their ability to induce immune responses in adult mice and for protection on neonate BALB/c mice born from females immunised by mucosal delivery of both peptides. METHODS: Adult BALB/c mice were intraperitoneally immunised with SA35 and SA40, separately or mixed, and their immune response was characterised. Furthermore, BALB/c pregnant mice were immunised by mucosal delivery with an SA35/40 mix, before and during pregnancy. Soon after birth, their offspring were infected with two doses (1 × 10(5) and 5 × 10(3)) of C. parvum oocysts and the parasitic burden was determined at 5 and 9 days post-infection. RESULTS: Intraperitoneal immunisation with SA35 and SA40 induced specific IgG and IgG1 in serum, specific IgA in the intestinal mucosa, increase of CD3+/CD4+ and CD30+ cells in splenocytes, which produced IFN-γ. Neonates born from immunised mice and infected with 1 × 10(5) oocysts showed a significant reduction of oocysts and intestinal forms (23 and 42%, respectively). A reduction of all parasitic forms (96%; P < 0.05) was observed when neonates were infected with 5 × 10(3) oocysts. CONCLUSIONS: SA35 and SA40 peptides induce specific humoral and cell-mediated immune responses to C. parvum in adult mice. Moreover, mucosal administration of the SA35/40 mix in pregnant mice reduces C. parvum burden in their litters. url: https://doi.org/10.1186/s13071-019-3486-8 doi: 10.1186/s13071-019-3486-8 id: cord-308461-4lhh3du0 author: Ueki, Hiroshi title: Multicolor two-photon imaging of in vivo cellular pathophysiology upon influenza virus infection using the two-photon IMPRESS date: 2020-01-29 words: 8337 sentences: 517 pages: flesch: 47 cache: ./cache/cord-308461-4lhh3du0.txt txt: ./txt/cord-308461-4lhh3du0.txt summary: Unlike ex vivo methods, which involve isolated or sliced lungs, in vivo imaging using two-photon excitation microscopy of live animals enables researchers to observe hemodynamics, migration and extravasation of immune cells, as well as interactions among immune cells during influenza virus infection. To detect multiple fluorescent signals excited simultaneously by a two-photon excitation laser, fluorochromes with different spectra and equal brightness must be selected; however, there is currently no comprehensive database of fluorescent reagents, fluorescent reporter viruses, and reporter mouse lines available for lung in vivo imaging. Our system uses suction-based lung stabilization 16, 28 to improve an existing in vivo two-photon imaging system for influenza virus-infected lung as a model of an acute inflammatory respiratory disease 5 . In vivo two-photon imaging is performed under conditions of single stimulation with a two-photon excitation laser; limitations exist regarding available fluorescent reagents/proteins for multiple labeling of target cells and lung architecture. abstract: In vivo two-photon imaging is a valuable technique for studies of viral pathogenesis and host responses to infection in vivo. In this protocol, we describe a methodology for analyzing influenza virus–infected lung in vivo by two-photon imaging microscopy. We describe the surgical procedure, how to stabilize the lung, and an approach to analyzing the data. Further, we provide a database of fluorescent dyes, antibodies, and reporter mouse lines that can be used in combination with a reporter influenza virus (Color-flu) for multicolor analysis. Setup of this model typically takes ~30 min and enables the observation of influenza virus–infected lungs for >4 h during the acute phase of the inflammation and at least 1 h in the lethal phase. This imaging system, which we termed two-photon IMPRESS (imaging pathophysiology research system), is broadly applicable to analyses of other respiratory pathogens and reveals disease progression at the cellular level in vivo. url: https://doi.org/10.1038/s41596-019-0275-y doi: 10.1038/s41596-019-0275-y id: cord-259364-8zoav7b0 author: Xiao, Yire title: Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis date: 2019-09-09 words: 4494 sentences: 247 pages: flesch: 56 cache: ./cache/cord-259364-8zoav7b0.txt txt: ./txt/cord-259364-8zoav7b0.txt summary: title: Production of anti-Trichophyton rubrum egg yolk immunoglobulin and its therapeutic potential for treating dermatophytosis The aim of this study was to estimate the therapeutic potential of specific egg yolk immunoglobulin (IgY) on dermatophytosis caused by Trichophyton rubrum. rubrum cell wall proteins IgY (anti-trCWP IgY) presented a certain degree of cross-reactivity with different fungi. In the in vitro and in vivo activity researches, Anti-trCWP IgY showed a significant dose-dependent growth inhibitory effect on T. To estimate the cross-reactivity (CR) of anti-trCWP IgY against other fungi, indirect ELISAs were performed by the use of antigens from different fungi according to the method described previously. rubrum and the protective effect of anti-trCWP IgY against dermatophytosis of experimentally infected mice. In our study, the cell wall proteins showed good immunogenicity, highest titer of anti-trCWP IgY reaching 1:16000. rubrum in a dose-dependent manner compared with IgY from unimmunized hens,and significantly reduced lesion scores of mice experimentally infected with T. abstract: The aim of this study was to estimate the therapeutic potential of specific egg yolk immunoglobulin (IgY) on dermatophytosis caused by Trichophyton rubrum. The IgY was produced by immunizing hens with cell wall proteins of T. rubrum, extracted from eggs by PEG precipitation and then purified by ammonium sulfate precipitation. The cross-reactivity (CR) with other fungi, growth inhibition on T. rubrum in vitro and therapeutic effect on T. rubrum infection in BALB/C mice of the specific IgY were then evaluated. Anti- T. rubrum cell wall proteins IgY (anti-trCWP IgY) presented a certain degree of cross-reactivity with different fungi. In the in vitro and in vivo activity researches, Anti-trCWP IgY showed a significant dose-dependent growth inhibitory effect on T. rubrum in vitro and a significant dose-dependent therapeutic effect on T. rubrum infection in BALB/C mice. url: https://api.elsevier.com/content/article/pii/S0882401018307204 doi: 10.1016/j.micpath.2019.103741 id: cord-259094-5qzbctan author: Xu, Mei Ling title: The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection date: 2013-04-26 words: 2514 sentences: 142 pages: flesch: 54 cache: ./cache/cord-259094-5qzbctan.txt txt: ./txt/cord-259094-5qzbctan.txt summary: title: The effect of dietary intake of the acidic protein fraction of bovine colostrum on influenza A (H1N1) virus infection In this study, we isolated the acidic protein fraction of bovine colostrum (AFC, isoelectric point <5) by anion-exchange chromatography, and investigated the effect of its dietary intake on influenza A (H1N1) virus infection. In this study we isolated the acidic protein fraction of bovine colostrum (AFC) and investigated how dietary intake of AFC modulates the symptoms of influenza infection. The three mouse groups were given oseltamivir, PBS and AFC orally for 14 days prior to infection with influenza A virus. Therefore, the effect of total bovine colostrums on influenza virus infection in mice was significantly different from our expectation. In this study, we provide the first evidence that orally supplemented AFC is effective in reducing the symptoms associated with influenza A virus infection. abstract: Acidic protein levels in the milk decrease markedly as lactation progresses, suggesting that it is an important part of the colostrum. However, little attention has been paid to their biological function. In this study, we isolated the acidic protein fraction of bovine colostrum (AFC, isoelectric point <5) by anion-exchange chromatography, and investigated the effect of its dietary intake on influenza A (H1N1) virus infection. 100% of mice infected with 1 LD(50) of the virus survived when administered AFC for 14 days prior to infection, compared with 33% survival when administered phosphate buffered saline (PBS). Moreover, consumption of AFC reduced the weight loss associated with infection. We propose that dietary intake of AFC has a prophylactic effect on influenza A virus infection. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s12275-013-2683-y and is accessible for authorized users. url: https://doi.org/10.1007/s12275-013-2683-y doi: 10.1007/s12275-013-2683-y id: cord-275779-ocbygkyb author: Ye, Zi-Wei title: Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice date: 2017-03-21 words: 5425 sentences: 253 pages: flesch: 42 cache: ./cache/cord-275779-ocbygkyb.txt txt: ./txt/cord-275779-ocbygkyb.txt summary: title: Antibody-Dependent Cell-Mediated Cytotoxicity Epitopes on the Hemagglutinin Head Region of Pandemic H1N1 Influenza Virus Play Detrimental Roles in H1N1-Infected Mice Engaging the antibody-dependent cell-mediated cytotoxicity (ADCC) for killing of virus-infected cells and secretion of antiviral cytokines and chemokines was incorporated as one of the important features in the design of universal influenza vaccines. In this study, we determined the ADCC and antiviral activities of two putative ADCC epitopes, designated E1 and E2, on the HA head of a pandemic H1N1 influenza virus in vitro and in a lethal mouse model. The phenotype was potentially due to an exaggerated inflammatory cell infiltration triggered by ADCC, as an upregulated release of cytotoxic granules (perforin) was observed in the lung tissue of E1-vaccinated mice after H1N1 influenza virus challenge. While the antiviral efficacy provided by the stalk-specific ADCC antibodies has been confirmed (12) , our data raised concerns on the side effect of certain HA head epitopes in devising a universal influenza vaccine. abstract: Engaging the antibody-dependent cell-mediated cytotoxicity (ADCC) for killing of virus-infected cells and secretion of antiviral cytokines and chemokines was incorporated as one of the important features in the design of universal influenza vaccines. However, investigation of the ADCC epitopes on the highly immunogenic influenza hemagglutinin (HA) head region has been rarely reported. In this study, we determined the ADCC and antiviral activities of two putative ADCC epitopes, designated E1 and E2, on the HA head of a pandemic H1N1 influenza virus in vitro and in a lethal mouse model. Our data demonstrated that sera from the E1-vaccinated mice could induce high ADCC activities. Importantly, the induction of ADCC response modestly decreased viral load in the lungs of H1N1-infected mice. However, the elevated ADCC significantly increased mouse alveolar damage and mortality than that of the PBS-vaccinated group (P < 0.0001). The phenotype was potentially due to an exaggerated inflammatory cell infiltration triggered by ADCC, as an upregulated release of cytotoxic granules (perforin) was observed in the lung tissue of E1-vaccinated mice after H1N1 influenza virus challenge. Overall, our data suggested that ADCC elicited by certain domains of HA head region might have a detrimental rather than protective effect during influenza virus infection. Thus, future design of universal influenza vaccine shall strike a balance between the induction of protective immunity and potential side effects of ADCC. url: https://doi.org/10.3389/fimmu.2017.00317 doi: 10.3389/fimmu.2017.00317 id: cord-275635-d50bxe7c author: Yuan, Xiaomin title: Efficacy and immunogenicity of recombinant swinepox virus expressing the A epitope of the TGEV S protein date: 2015-07-31 words: 3979 sentences: 212 pages: flesch: 54 cache: ./cache/cord-275635-d50bxe7c.txt txt: ./txt/cord-275635-d50bxe7c.txt summary: To explore the possibility of developing a vaccine against transmissible gastroenteritis virus (TGEV) infection, a recombinant swinepox virus (rSPV-SA) expressing a TGEV protective antigen has been constructed. Results from the passive immunity protection test of new born piglets demonstrated that the recombinant live-vector vaccine, rSPV-SA, could 100% protect piglets from the SPV infection, and there was no significant clinical symptom in the rSPV-SA treatment group during this experiment. Eight one-month-old swine (Large White) were randomly divided into four groups (2 pigs per group) and were immunized twice at 0 and 28 days with infectious rSPV-SA (1 × 10 8 PFU/ml in 2 ml of PBS), inactivated-TGEV (1 × 10 8 PFU/ml in 2 ml of PBS), wtSPV (1 × 10 8 PFU/ml in 2 ml of PBS) or PBS, each time via three routes: oral, nasal, and intraperitoneal. To explore whether mice or swine generated TGEV neutralizing antibodies, serum from the PBS, wtSPV, inactivated-TGEV and rSPV-SA treated mice and pig were collected at 0, 14, 21, 35, 42 days post-primary immunization (1:100-1:12,800 dilution in a 100 l volume). abstract: To explore the possibility of developing a vaccine against transmissible gastroenteritis virus (TGEV) infection, a recombinant swinepox virus (rSPV-SA) expressing a TGEV protective antigen has been constructed. Immune responses and protection efficacy of the vaccination vector were assessed in both mice and pig models. An indirect ELISA assay suggested that when mice were vaccinated with rSPV-SA, the level of IgG against TGEV was enhanced dramatically. The cytokine assays were employed and the results indicated that both the Th1-type and Th2-type cytokine levels raised after vaccination with rSPV-SA in mice models. Results from the passive immunity protection test of new born piglets demonstrated that the recombinant live-vector vaccine, rSPV-SA, could 100% protect piglets from the SPV infection, and there was no significant clinical symptom in the rSPV-SA treatment group during this experiment. The data suggest that the novel recombinant swinepox virus is a potential vaccine against TGEV infection. url: https://doi.org/10.1016/j.vaccine.2015.06.057 doi: 10.1016/j.vaccine.2015.06.057 id: cord-347661-q9lgliph author: Zevenhoven-Dobbe, Jessika C. title: Production of Monospecific Rabbit Antisera Recognizing Nidovirus Proteins date: 2007-11-28 words: 6866 sentences: 343 pages: flesch: 53 cache: ./cache/cord-347661-q9lgliph.txt txt: ./txt/cord-347661-q9lgliph.txt summary: The use as antigens of either synthetic peptides (coupled to a carrier protein) or proteins expressed in Escherichia coli is described, and detailed protocols for immunization and preparation of test bleeds are provided. Furthermore, in the context of specific research questions, polyclonal antisera may sometimes even be preferred over monoclonal antibodies since they contain a mixture of immunoglobulin molecules, derived from different B-cell lines in the immunized animal, often recognizing multiple epitopes of the target protein. The antiserum used here was raised against a domain in the C-terminal region of pp1a of the arterivirus EAV (8) and recognizes a large set of processing intermediates and end products, which are indicated by arrowheads: (A) Western blot analysis: EAV-and mock-infected cell lysates were prepared at 8 h postinfection, run on an SDS-polyacrylamide gel, blotted to PVDF membrane, and incubated with the postimmune serum at a 1:1000 dilution. abstract: The importance of monospecific antisera for the experimental analysis of viral proteins is undisputed. They make it possible to identify and analyze the target protein against a background of a large number of other proteins, either in whole fixed cells or in cell lysates. This chapter describes our experience with the production of such rabbit antisera directed against proteins of coronaviruses and other nidoviruses. The use as antigens of either synthetic peptides (coupled to a carrier protein) or proteins expressed in Escherichia coli is described, and detailed protocols for immunization and preparation of test bleeds are provided. For screening of the immune response following immunization, detailed protocols for three commonly used techniques are described, all of which are based on the use of infected cells or cells expressing the protein of interest, side by side with appropriate controls. The in situ immunodetection of the target in fixed cells by immunofluorescence microscopy is described, as are protocols for techniques that can be applied to cell lysates containing the target protein (Western blotting and immunoprecipitation). The latter techniques are performed in combination with polyacrylamide gel electrophoresis, thus allowing confirmation of the molecular weight of the target that is recognized by the antiserum. url: https://www.ncbi.nlm.nih.gov/pubmed/19057875/ doi: 10.1007/978-1-59745-181-9_16 id: cord-002013-rb9xdzro author: Zheng, Xuexing title: Treatment with hyperimmune equine immunoglobulin or immunoglobulin fragments completely protects rodents from Ebola virus infection date: 2016-04-12 words: 6027 sentences: 286 pages: flesch: 56 cache: ./cache/cord-002013-rb9xdzro.txt txt: ./txt/cord-002013-rb9xdzro.txt summary: To investigate whether EBOV infections can be controlled by virus neutralization alone, and to prevent the possible induction of serum sickness in humans that would be administered antisera, the post-exposure efficacy of F(ab′ ) 2 (immunoglobulin treated with pepsin to remove the Fc regions of the antibody) were also investigated side-by-side with equine antisera in all experiments as a potential alternate treatment. Three horses were immunized intramuscularly (IM) with 7 injections of eVLP over 11 weeks and the hyperimmune sera were collected from each animal at specified timepoints ( Fig. 1A) to determine the serum titers by neutralization assay against a recombinant HIV-1 virus pseudotyped with EBOV GP. The observation that administering F(ab′ ) 2 at 1 dpi is more efficacious than when the same treatment was given at 30 minutes post-exposure (Fig. 5A ) was also observed in past studies with therapeutic EBOV GP-specific monoclonal antibodies 25, 26 , and suggests that virus neutralization may play a bigger role in protection at a later timepoint after EBOV challenge. abstract: Recent successes with monoclonal antibody cocktails ZMapp(TM) and MIL77 against Ebola virus (EBOV) infections have reignited interest in antibody-based therapeutics. Since the production process for monoclonal antibodies can be prolonged and costly, alternative treatments should be investigated. We produced purified equine antisera from horses hyperimmunized with EBOV virus-like particles, and tested the post-exposure efficacy of the antisera in a mouse model of infection. BALB/c mice were given up to 2 mg of purified equine antisera per animal, at 30 minutes, 1 or 2 days post-infection (dpi), in which all animals survived. To decrease the possibility of serum sickness, the equine antisera was digested with pepsin to generate F(ab′)(2) fragments, with in vitro neutralizing activity comparable to whole immunoglobulin. Full protection was achieved with when treatment was initiated at 1 dpi, but the suboptimal protection observed with the 30 minute and 2 dpi groups demonstrate that in addition to virus neutralization, other Fc-dependent antibody mechanisms may also contribute to survival. Guinea pigs given 20 mg of antisera or F(ab′)(2) at or starting at 1 or 2 dpi were also fully protected from EBOV infection. These results justify future efficacy studies for purified equine products in NHPs. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828711/ doi: 10.1038/srep24179 id: cord-278802-bverdk5w author: Zhou, Yefei title: Immune response of AA broilers to IBV H120 vaccine and sodium new houttuyfonate date: 2010-12-31 words: 3161 sentences: 177 pages: flesch: 57 cache: ./cache/cord-278802-bverdk5w.txt txt: ./txt/cord-278802-bverdk5w.txt summary: On 0, 7, 14, 21, 28 and 35 post first vaccination, the dynamic changes of peripheral lymphocyte proliferation, cytokine assays and serum antibody titers were assayed respectively by MTT method, ELISA and hemagglutination inhibition assay (HI). The results showed that sodium new houttuyfonate significantly raised IB antibody titer in the chickens and also markedly promoted lymphocyte proliferation. Five chickens were sampled randomly from each group for assay of lymphocyte proliferation by MTT method and 10 chickens from each group for assessment of serum HI antibody titer by the micro-method and cytokines by ELISA kits at 0, 7, 14, 21 and 35 days post the primary immunization (dpi). In this study, with chicken IBV H120 strain live attenuated vaccine in chickens, by measuring peripheral blood lymphocyte proliferation and serum cytokines and antibody titers, the humoral and cellular immunity induced with SNH was researched. abstract: Abstract In this report, 120 healthy one-day-old AA broilers were divided into six groups. Groups 1–4 received 100, 200, 400 and 800mg/L of sodium new houttuyfonate (SNH) with IB vaccine H120 respectively. Group 5 received PBS and H120 and group 6 IL-2 and H120. The chickens were inoculated at 7 and 14days of age. On 0, 7, 14, 21, 28 and 35 post first vaccination, the dynamic changes of peripheral lymphocyte proliferation, cytokine assays and serum antibody titers were assayed respectively by MTT method, ELISA and hemagglutination inhibition assay (HI). The results showed that sodium new houttuyfonate significantly raised IB antibody titer in the chickens and also markedly promoted lymphocyte proliferation. The serum levels of IFN-γ and IL-4 in groups 1–4 were higher than those in groups 5 and 6. Hence, the immunologic enhancement of SNH was slightly superior to that of IL-2 adjuvant. Following challenge with IBV, chickens inoculated with SNH showed fewer and less severe clinical signs, lower death rate and less kidney pathology, as compared to those of the control groups. It indicated that SNH could enhance immune responses and increase protection against virulent IBV challenge in chickens. url: https://doi.org/10.1016/j.rvsc.2010.04.010 doi: 10.1016/j.rvsc.2010.04.010 id: cord-002583-cgcf7mgj author: Zhuo, Xun-hui title: Evaluation of potential anti-toxoplasmosis efficiency of combined traditional herbs in a mouse model date: 2017-06-01 words: 3785 sentences: 197 pages: flesch: 57 cache: ./cache/cord-002583-cgcf7mgj.txt txt: ./txt/cord-002583-cgcf7mgj.txt summary: The results showed that the survival time of mice in the 500 mg Chinese herbs group and sulfadiazine group was significantly longer than that of the PBS control group. Also the parasite load in blood and tissues of 500 mg Chinese herbs and sulfadiazine groups was significantly lower than that of PBS group at 7 days post infection (dpi), which was in accordance with the result of histological detection. Results of spleen, lung, and liver tissues presented a similar pattern in that parasite loads were all largely increased from 3 to 7 dpi, and mice of the PBS control group had statistically significantly higher parasite load compared with sulfadiazine and 500 mg Chinese herb groups (P<0.05). The lungs of sulfadiazine and Chinese herbs-treated mice possessed a significantly lower parasite load than that of the PBS control group (P<0.05) and the histological result verified this from the morphological perspective. abstract: Toxoplasma gondii is a worldwide spread protozoan and is able to infect almost all warm-blood animals. No effective drugs are available clinically on toxoplasmosis. Chinese traditional herbal medicines have provided remedies for many health problems. There exists a possibility that Chinese herbs may provide protection against T. gondii. This work aims to assess the protective efficacy of combined Chinese herbs against T. gondii. We screened five herbal medicines that have different pharmacological effects and combined them into a prescription according to the traditional Chinese medicine compatibility principle. The drug potential and protective efficacy were evaluated through a mouse model by determining the survival time, the parasite load in blood and tissues, the change of cell proportions in blood and histological detection. The results showed that the survival time of mice in the 500 mg Chinese herbs group and sulfadiazine group was significantly longer than that of the PBS control group. Also the parasite load in blood and tissues of 500 mg Chinese herbs and sulfadiazine groups was significantly lower than that of PBS group at 7 days post infection (dpi), which was in accordance with the result of histological detection. Monocyte and neutrophil of infected mice were remarkably increased while lymphocyte was dramatically decreased compared to that of blank group at 7 dpi. The results demonstrated that the 500 mg dosage of our Chinese herbs could slow down the replication of T. gondii and prolong the survival time of mice and could be considered as possible candidate drug against toxoplasmosis. url: https://link.springer.com/content/pdf/10.1631/jzus.B1600316.pdf doi: 10.1631/jzus.b1600316 id: cord-333639-usgpe1cz author: Zuwala, Kaja title: Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects date: 2018-04-10 words: 9337 sentences: 493 pages: flesch: 48 cache: ./cache/cord-333639-usgpe1cz.txt txt: ./txt/cord-333639-usgpe1cz.txt summary: title: Macromolecular prodrugs of ribavirin: Polymer backbone defines blood safety, drug release, and efficacy of anti-inflammatory effects We focus on the choice of the macromolecular backbone as a carrier for the conjugated drug and analyze blood coagulation, binding to albumin, albumin aggregation, inhibitory activity on polymerases, and cytotoxicity for polymers differed by their anionic charge (carboxylates, phosphates and phosphonates, sulfonates). As a result, we identify polymers and macromolecular prodrugs that are devoid of blood anti-coagulation activity but are strong as inhibitors of polymerases and efficacious as delivery vehicles for ribavirinthus being attractive for the development of broad-spectrum antiviral agents. This observation echoes our recent findings on the apparent unique pairing of negative character and hydrophobicity of the polymer backbone that renders PEAA an efficacious inhibitor of e.g. hepatitis C virus intracellular replication [55] and a lead polymer with broad-spectrum antiviral activity [21] . Polyanionic macromolecular prodrugs of ribavirin: antiviral agents with a broad Spectrum of activity abstract: Macromolecular (pro)drugs hold much promise as broad-spectrum antiviral agents as either microbicides or carriers for intracellular delivery of antiviral drugs. Intriguing opportunity exists in combining the two modes of antiviral activity in the same polymer structure such that the same polymer acts as a microbicide and also serves to deliver the conjugated drug (ribavirin) into the cells. We explore this opportunity in detail and focus on the polymer backbone as a decisive constituent of such formulations. Fourteen polyanions (polycarboxylates, polyphosphates and polyphosphonates, and polysulfonates) were analyzed for blood pro/anti coagulation effects, albumin binding and albumin aggregation, inhibitory activity on polymerases, cytotoxicity, and anti-inflammatory activity in stimulated macrophages. Ribavirin containing monomers were designed to accommodate the synthesis of macromolecular prodrugs with disulfide-exchange triggered drug release. Kinetics of drug release was fast in all cases however enhanced hydrophobicity of the polymer significantly slowed release of ribavirin. Results of this study present a comprehensive view on polyanions as backbone for macromolecular prodrugs of ribavirin as broad-spectrum antiviral agents. url: https://doi.org/10.1016/j.jconrel.2018.02.012 doi: 10.1016/j.jconrel.2018.02.012 id: cord-000354-05lnj3w0 author: de Vries, Erik title: Dissection of the Influenza A Virus Endocytic Routes Reveals Macropinocytosis as an Alternative Entry Pathway date: 2011-03-31 words: 10971 sentences: 561 pages: flesch: 48 cache: ./cache/cord-000354-05lnj3w0.txt txt: ./txt/cord-000354-05lnj3w0.txt summary: The sensitivity of the dynamin-independent entry pathway to inhibitors or dominant-negative mutants affecting actomyosin dynamics as well as to a number of specific inhibitors of growth factor receptor tyrosine kinases and downstream effectors thereof all point to the involvement of macropinocytosis in IAV entry. As factors present in serum are known for their potential to induce specific endocytic pathways, we further explored the conditions required for the novel DYNA-IND IAV entry pathway (using the Gluc-entry assay) by inoculating cells in PBS in the presence of increasing concentrations of fetal calf serum (FCS). Growth factor inducible activation of the tyrosine kinase src has also been linked to the induction of macropinocytosis [49] [50] [51] ; consistent with this observation the src inhibitor PP2 [52] specifically inhibited DYNA-IND entry of IAV (Fig. 9A-B) . abstract: Influenza A virus (IAV) enters host cells upon binding of its hemagglutinin glycoprotein to sialylated host cell receptors. Whereas dynamin-dependent, clathrin-mediated endocytosis (CME) is generally considered as the IAV infection pathway, some observations suggest the occurrence of an as yet uncharacterized alternative entry route. By manipulating entry parameters we established experimental conditions that allow the separate analysis of dynamin-dependent and -independent entry of IAV. Whereas entry of IAV in phosphate-buffered saline could be completely inhibited by dynasore, a specific inhibitor of dynamin, a dynasore-insensitive entry pathway became functional in the presence of fetal calf serum. This finding was confirmed with the use of small interfering RNAs targeting dynamin-2. In the presence of serum, both IAV entry pathways were operational. Under these conditions entry could be fully blocked by combined treatment with dynasore and the amiloride derivative EIPA, the hallmark inhibitor of macropinocytosis, whereas either drug alone had no effect. The sensitivity of the dynamin-independent entry pathway to inhibitors or dominant-negative mutants affecting actomyosin dynamics as well as to a number of specific inhibitors of growth factor receptor tyrosine kinases and downstream effectors thereof all point to the involvement of macropinocytosis in IAV entry. Consistently, IAV particles and soluble FITC-dextran were shown to co-localize in cells in the same vesicles. Thus, in addition to the classical dynamin-dependent, clathrin-mediated endocytosis pathway, IAV enters host cells by a dynamin-independent route that has all the characteristics of macropinocytosis. url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068995/ doi: 10.1371/journal.ppat.1001329 ==== make-pages.sh questions [ERIC WAS HERE] ==== make-pages.sh search /data-disk/reader-compute/reader-cord/bin/make-pages.sh: line 77: /data-disk/reader-compute/reader-cord/tmp/search.htm: No such file or directory Traceback (most recent call last): File "/data-disk/reader-compute/reader-cord/bin/tsv2htm-search.py", line 51, in with open( TEMPLATE, 'r' ) as handle : htm = handle.read() FileNotFoundError: [Errno 2] No such file or directory: '/data-disk/reader-compute/reader-cord/tmp/search.htm' ==== make-pages.sh topic modeling corpus Zipping study carrel