key: cord-0720808-xty16m8w
authors: Marrugal-Lorenzo, José A.; Serna-Gallego, Ana; Berastegui-Cabrera, Judith; Pachón, Jerónimo; Sánchez-Céspedes, Javier
title: Repositioning salicylanilide anthelmintic drugs to treat adenovirus infections
date: 2019-01-09
journal: Sci Rep
DOI: 10.1038/s41598-018-37290-3
sha: 51340894a896316b58653a60c48da9c16b3ad0e3
doc_id: 720808
cord_uid: xty16m8w

The repositioning of drugs already approved by regulatory agencies for other indications is an emerging alternative for the development of new antimicrobial therapies. The repositioning process involves lower risks and costs than the de novo development of novel antimicrobial drugs. Currently, infections by adenovirus show a steady increment with a high clinical impact in immunosuppressed and immunocompetent patients. The lack of a safe and efficacious drug to treat these infections supports the search for new antiviral drugs. Here we evaluated the anti-adenovirus activity of niclosanide, oxyclozanide, and rafoxanide, three salicylanilide anthelmintic drugs. Also, we carried out the cytotoxicity evaluation and partial characterization of the mechanism of action of these drugs. The salicylanilide anthelmintic drugs showed significant anti-adenovirus activity at low micromolar concentrations with little cytotoxicity. Moreover, our mechanistic assays suggest differences in the way the drugs exert anti-adenovirus activity. Niclosamide and rafoxanide target transport of the HAdV particle from the endosome to the nuclear envelope, whilst oxyclozanide specifically targets adenovirus immediately early gene E1A transcription. Data suggests that the studied salicylanilide anthelmintic drugs could be suitable for further clinical evaluation for the development of new antiviral drugs to treat infections by adenovirus in immunosuppressed patients and in immunocompetent individuals with community-acquired pneumonia.

Anti-adenovirus activity of salicylanilide anthelmintic drugs. In initial studies, we determined the inhibitory concentrations of the three anthelmintic drugs against HAdV in a plaque assay measured as the percentage of plaque formation inhibition compared to a control cells infected in the absence of drugs. The three salicylanilide anthelmintic drugs showed a dose-dependent anti-HAdV activity against both HAdV5 and HAdV16, with 100% inhibition of plaques formation at 1.25, 5 and 2.5 μM for NIC, OXY and RAF, respectively ( Fig. 2a,b) . The IC 50 values for the three anthelmintic drugs are summarized in Table 1 . We also evaluated whether these salicylanilide anthelmintic drugs were able to inhibit virus production using HAdV5, HAdV16 and HAdV19 yield reduction assays. Treatment with NIC, OXY and RAF was associated with overall reductions in virus yield from 10 to 186-fold (Table 1) .

In an assay measuring antiviral activity of the three anthelmintic drugs as a function of MOI, inhibition was inversely proportional to the number of input particles (Fig. 3 ). While they were also inhibitory at high MOI, the relationship between the number of infecting HAdV particles and the drugs concentration is less marked, as expected.

The cellular cytotoxicity of the salicylanilide drugs was also analyzed. The CC 50 values for these molecules were in all cases significantly higher than the IC 50 concentrations required for inhibition in our antiviral activity and mechanistic assays for both 293β5 cells (Table 1 ) and A549 cells (22.9 ± 9.8 µM, 76.1 ± 14.4 µM and 80.6 ± 34.7 µM for NIC, OXY and RAF, respectively).

Step in HAdV replicative cycle. As the first step toward identifying the specific step in the HAdV replicative cycle that was inhibited by these drugs, we measured the time dependence of the three anthelmintic drugs addition on their ability to block HAdV infection. A previous report showed biochemically that HAdV viral particles were internalized within 5 min of binding and reach the nuclear pore after 45 min 18 . Our results demonstrated that NIC, OXY and RAF exhibited a time-dependent decrease in their inhibitory activity (Fig. 4a) . All of them showed high inhibition of HAdV infection when added at the beginning of the 60 min incubation at 4 °C (−60 min), and when added immediately prior to warming (0 min) or after 10 min. However, when drugs were added at 60 or 120 min, only OXY still showed a significant inhibition higher than 50% which was lost for NIC and RAF (Fig. 4a) .

To support these findings a western blotting for HAdV E1A protein was run at 6 h post infection. Results obtained showed a significantly lower expression of E1A protein in samples treated with NIC and RAF compared with OXY (Fig. 4b) .

Impact on HAdV genome accessibility to the nucleus. This assay evaluated the impact of the salicylanilide anthelmintic drugs on HAdV endosomal escape. After the binding and internalization of the HAdV viral particles, the exposure of protein VI inside the endosome triggers endosomolysis and the partially decapsidated HAdV escape to the cytosol from where it is transported to the nuclear pore complex at the nuclear membrane by the microtubule network. We used a functional assay comprising HAdV-mediated co-delivery of α-sarcin in cells as a marker of the ability of these salicylanilide drugs to alter virus-mediated endosomolysis 19, 20 . No significant differences in the ID 50 (50% inhibitory doses) for HAdV-mediated endosome penetration were detected in the presence of any of the salicylanilide drugs ( Fig. 5 ) or the DMSO negative control. In contrast, the control virus Ad5ts1, an endosome penetration-defective mutant, exhibited a significant increase in the ID 50 compared to the DMSO control (Fig. 5) .

Once viral particles leave the endosome they are transported to the nuclear pore complex where HAdV genomes are imported into the nucleus 21 . We hypothesized that if any of the drugs examined was blocking a step in the HAdV entry, as expected for NIC, the number of genomes that reach the nucleus would be lower. We next evaluated the ability of these salicylanilide drugs to block HAdV genome accessibility to the nucleus by the quantification of HAdV genomes isolated from the nucleus 22 . As reflected in Fig. 6a , only NIC and RAF showed a significant block in the accessibility of HAdV genomes to the nucleus (Fig. 6a) . The DNA copy number of the cellular gene GAPDH was also evaluated in both the nucleus and the cytoplasm as a control for the purity of nuclear isolation (data not shown). Since our results indicated that NIC and RAF hindered the accessibility of HAdV genome to the nucleus while OXY did not, we resolved to determine if this anthelmintic drug affected later steps in HAdV life cycle.

Impact on HAdV replication. The next step was to examine the effect that OXY had upon efficient HAdV DNA replication using quantitative real-time PCR (qPCR). A549 cells were infected with HAdV and incubated for 2 h at 37 °C. Then, the unbound virions were washed-out and cell cultures were incubated for 24 h. HAdV DNA was extracted at that point to limit the interference caused by subsequent rounds of infection occurring 32-36 h post-infection 23 . We used quantitative PCR to quantify in a single round of infection the synthesis of new HAdV DNA copies as a measure of DNA replication efficiency. The presence of OXY (25 μM) significantly inhibited HAdV5 DNA replication by more than 50% (p < 0.05, Dunnett's Multiple Comparison test), whilst the quantification of the DNA copies of the GAPDH gene did not showed a significant effect (Fig. 6b ). This reduction in the HAdV DNA copy number at the nucleus in the presence of OXY implicated two alternatives for its mechanism of action: i) OXY could inhibit HAdV DNA replication by interfering with a protein required in this process like HAdV DNA polymerase, DNA binding protein (DBP) or terminal protein (TP) or, alternatively, ii) OXY could impact transcription of the HAdV immediate early gene E1A, which is a key step before DNA replication.

To assay the inhibition of HAdV mRNA transcription, we infected A549 cells in the presence of OXY (25 μM) for 6 h. After the infection, we quantified the RNA copy number of the E1A gene using quantitative reverse transcription (RT-PCR). As shown in Fig. 6c , OXY exerted a significant decrease in the E1A mRNAs copy number compared with the control treated with DMSO.

Based on previous works where piperazine derivatives and nucleotide and nucleoside analogues showed antiviral activity against multiple dsDNA virus including cytomegalovirus (HCMV) and HAdV 24,25 , we evaluated the inhibitory activity of NIC, OXY and RAF on HCMV DNA replication. The presence of these anthelmintic drugs generated significant reductions in the quantification of total HCMV DNA 72 h after infection of MRC-5 cells (Fig. 6d ). OXY showed a 79% decrease whilst NIC and RAF reached a 98.3% and a 98.1% decrease, respectively of HCMV DNA replication, showing no significant differences between samples for the quantification of the GAPDH gene (data not shown).

Salicylanilide anthelmintic drugs combination improves their antiviral activity. Since we found different mechanisms of action for these three drugs we hypothesize that their combination should significantly improve their antiviral activity. To evaluate our hypothesis we conducted a combination study based on the Chou-Talalay method for drug combination using the CalcuSyn software 26, 27 . The constant ration for each combination was selected based on the IC 50 values for each drug. The data for all the combinations showed good conformity to the mass action law (r = 0.978-0.999) ( Table 2 ). All the combinations were classified as synergistic (Table 2 ). For the NIC:RAF (ratio 1:2) combination the IC 50 and IC 75 levels of inhibition were classified as synergism and the IC 90 level as strong synergism (Table 2 ). Finally, the combination RAF:OXY (ratio 1:2) was classified as synergism at all the levels of inhibition (Table 2 ).

The aim of this study was to evaluate the anti-HAdV activity of NIC, a salicylanilide anthelmintic drug of human use to set the basis for its further experimental and clinical development as a potential new treatment for HAdV infections. Moreover, we included in our evaluation other two chlorinated salicylanilide anthelmintic derivatives approved for animal use, OXY and RAF, because of their closely related structure and mechanism of action with NIC. It is well-known that these drugs act as uncouplers of the oxidative phosphorylation, involving dissipation of the membrane potential 28 . In case of NIC, Jurgeitr et al. 14 previously demonstrated that its antiviral mechanism of action was specifically associated with the neutralization of the endosomal pH, thus showing a broad antiviral activity against pH-dependent viruses. Although HAdV endosomal escape is not exclusively dependent of pH, a low pH has proven to be associated with the endosomal escape of HAdV 20, 29 . With these premises, we initially assumed a probable common anti-HAdV mechanism of action for these three drugs and decided to characterize their anti-HAdV activity as a previous step before the evaluation of their safety and efficacy in the Syrian hamster model of HAdV infection.

Here, we show that NIC, OXY and RAF exert significant anti-HAdV and anti-HCMV activity at low concentrations. To put this data into perspective, it is noteworthy that the reported IC 50 values for cidofovir, the drug of choice for the treatment of HAdV infections, are higher than those shown by these three salicylanilide drugs 30, 31 . In addition, following our own methodologies, the IC 50 value for cidofovir was 24.06 ± 5.9 µM, significantly higher than the values obtained for the three salicylanilide drugs. As for their mechanism of action, the data obtained from this work demonstrates that one of these three closely-related drugs did not share the expected mode of action. We have confirmed in our work that NIC, and as a novelty RAF, acts to decrease the number of HAdV genomes associated with the host nucleus, however, as demonstrated by our physiologic assay using the ribotoxin α-sarcin NIC and RAF may act in a later step after HAdV endosomal escape. Unlike NIC and RAF, OXY did not inhibit the access of HAdV genomes to the nucleus. This observation was confirmed in their time-course assay where we found that, for NIC and RAF inhibition occurred at earliest times of the HAdV replicative cycle than for OXY as well as in the western-blot assay at 6 hpi that showed higher inhibition of the E1A gene expression for NIC and RAF. As shown by our results, the high inhibition in the HAdV DNA replication generated by OXY may be the consequence of the previous and significant inhibition of the E1A gene transcription, which is supported by our results showing a clear inhibition of the E1A transcription at 6 hpi, both by quantitative real-time PCR and by western-blot. It is well known that prior to HAdV DNA replication, transcription of E1A by cellular RNA polymerase II takes place from the E1A promoter 32 . Then, E1A protein promotes its own transcription and is needed for the subsequent expression of the early genes E1B, E2, E3 and E4 from different promoters as well as for DNA replication and that is probably why we observed that significant inhibition on HAdV DNA replication. The existence of different mechanisms for the antiviral activity of these three drugs is supported by the significant combinatory index values obtained using the CalcuSyn software for all the drug combinations ( Table 2 ). The three anthelmintic drugs showed a moderate synergistic to a strong synergistic activity when they were combined in pairs, which was especially strong at all the levels of inhibition evaluated for the NIC-OXY combination. Likewise, using the combination of the three of them they showed a strong synergistic activity at all the levels of inhibition evaluated.

Repositioning of drugs for diseases different than those they were approved for is a valuable alternative for drug discovery and development since it reduces significantly the high cost and the time-consumption of developing a new drug [33] [34] [35] [36] . In case of NIC and other anthelmintic drugs, numerous reports support their repurposing as anti-cancer drugs due to their cancer inhibitory properties [37] [38] [39] [40] . NIC is an FDA-approved drug that has been used for many years to treat helminthic infections in humans and has previously demonstrated its antiviral potential against different viruses such as Japanese encephalitis flavivirus, zika virus, coronavirus, human rhinovirus or influenza virus [14] [15] [16] [17] . In rats, NIC is known to exert low in vivo toxicity, with a median lethal dose 50% (LD 50 ) of 5,000 mg/kg body weight and generate peak serum concentrations between 1.08 µM and 25 µM, depending on the dose and the administration route 40, 41 . In healthy humans orally treated with 750-2,000 mg NIC per person, no signs of intoxication were seen 42 , and the drug remained detectable for 1-2 days. Peak serum concentrations between 0.8-18 µM were reported 42, 43 . As shown in our results, these serum concentrations will be enough to reach the IC 50 for HAdV (Table 1) . OXY and RAF are other FDA-approved drugs for veterinary use to treat helminthic infections. For OXY, high serum concentrations ranging from 12.26 µM to 41.69 µM have been reported in sheep and goats after a single oral dose of 15 mg/kg 44 . In the case of RAF, an intravenous single dose of 10 mg/kg in goats generated serum concentrations ranging from 2.8 µM to 139.98 µM registered at 0.08 h and 12 h, respectively 45 . After a single oral dose of 22.5 mg/kg also in goats, the maximum serum concentrations obtained were 49.33 µM and 21.40 µM at 36 h and 168 h, respectively 45 . In both cases, OXY and RAF serum concentrations are significantly higher than their IC 50 for HAdV ( Table 1) . As for their toxicity, LD 50 of RAF has been reported to be higher than 2,000 mg/kg of body weight in rats while for OXY, according to the European Medicines Agency (EMEA), this LD 50 would be higher than 3,000 mg/kg of body weight (also in rats) 46 .

Our findings show a significant anti-HAdV activity for the three salicylanilide drugs targeting different steps on the HAdV life cycle. NIC and RAF would mainly block HAdV infection at some point between endosomal escape and DNA release into the nucleus, whilst the activity of OXY would be specifically targeting HAdV immediately early gene E1A transcription. Our findings support the evaluation of these three drugs in the Syrian hamster model of HAdV infection to evaluate their efficacy and safety. The pharmacokinetic profile of these salicylanilide drugs showing low water solubility and oral bioavailability may hamper its further clinical development 39 . In this situation, the generation of derivatives of these salicylanilide drugs based on rational chemical approaches may improve their poor pharmacokinetics, increasing their solubility and bioavailability as potential clinical candidates for antiviral therapy. Wild-type HAdV5 (species C), HAdV16 (species B), HAdV19 (species D), and human cytomegalovirus (HCMV) AD169 were obtained from the ATCC. The HAdV5-GFP and HAdV16-GFP used in this study are replication-defective viruses with a CMV promoter-driven enhanced green fluorescent protein (eGFP) reporter gene cassette in place of the E1/E3 region 48 . HAdV were propagated in 293β5 cells and isolated from the cellular lysate by cesium chloride (CsCl) density gradient combined with ultracentrifugation. Virus concentration in mg/ mL was calculated using the Bio-Rad Protein Assay (Bio-Rad Laboratories) and converted to virus particles/mL (vp/mL) using 4 × 10 12 vp/mg. Cytotoxicity assay. NIC, OXY and RAF cytotoxicity was evaluated using the Alamar Blue Cell Viability Assay (Invitrogen) according to the manufacturer's instructions. Actively dividing A549 or 293β5 cells were incubated with the salicylanilide anthelmintic drugs for 48 h. After this incubation, the Alamar Blue Reagent was added to the cells (1/10th Alamar Blue Reagent in culture medium) for an extra 4 h. Their 50% cytotoxic concentration (CC 50 ) was calculated as previously reported by Cheng et al. 49 . The selectivity index (SI) was calculated as the ratio of CC 50 to IC 50 , where the IC 50 is defined as the concentration of the anthelmintic drug that inhibits HAdV infection by 50%.

HAdV plaque assay. Anthelmintic drugs were tested in a dose-response assay using an MOI of 0.06 vp/cell and drug concentrations ranging from 10 to 0.1 μM in a plaque assay. Briefly, a density of 4 × 10 5 293β5 cells per well were seeded in 6-well plates. At 80-90% confluency they were infected with HAdV5-GFP or HAdV16-GFP (0.06 vp/cell) and rocked for 2 h at 37 °C. After this incubation wells were washed-out with PBS. Then, cells were carefully overlaid with 4 mL/well of equal parts of 1.6% (water/vol) Difco Agar Noble (Becton, Dickinson & Co., Sparks, MD) and 2× EMEM (Minimum Essential Medium Eagle, BioWhittaker) supplemented with 2 × penicillin/streptomycin, 2× L-glutamine, and 10% FBS. The mixture also contained the drugs in concentrations ranging from 10 to 0.15 μM. After incubation for 7 days at 37 °C, virus plaques were scanned with a Typhoon 9410 imager (GE Healthcare Life Sciences), and quantified with ImageJ 50 .

To determine the time course of the three anthelmintic drugs-mediated inhibition, parallel samples of wild-type HAdV5 were incubated with or without 5 μM of NIC and 25 μM of RAF or OXY in complete DMEM at 4 °C for 1 h. Virus (100 vp/cell) was then added to A549 cells (150,000 cells/well in a 24-well plate) and incubated at 37 °C. Anthelmintic drugs were added at the indicated time points (−60, 0, 10, 60, 120 and 360 min) before or during this incubation. After incubation at 37 °C and 5% CO 2 for 24 h DNA was purified from the cell lysate using the QIAamp DNA Mini Kit (QIAGEN, Valencia, CA) following the manufacturer's instructions, and the DNA was quantified by quantitative PCR following the above described protocol.

Analysis of anthelmintic drug combinations. The software packet Calcusyn (BioSoft, Ferguson, MO, USA), which compares the drug concentrations required in combination to generate a given effect to the drug concentration that would be needed individually to achieve that same effect was used. For this assay a plaque dose-response assay was carried out using all the possible combination of the three drugs starting from twice the IC 50 obtained previously for each compound and the ratio of those concentrations. CalcuSyn software interpolates the drugs concentrations needed in combination at the selected ratio to generate effects of 50%, 75% and 90% inhibition and compares these combined drug concentrations with the concentrations from the three drugs' individual dose-response curves required to achieve the same inhibition. The combination effect of the three drugs was reported by the combination index (CI) value, a quantitative estimation of the pharmacological interaction which uses the potency (IC 50 ) and the shape of the dose-response curve of each individual drug and their combinations. The CI value was interpreted in accordance with Matthews et al. 27 .

Nuclear-associated HAdV genomes. The nuclear accessibility of HAdV genomes was evaluated by real-time PCR following a previously described protocol with a few modifications 22 . Briefly, 1 × 10 6 A549 cells in 6-well plates were infected with wild-type HAdV5 (MOI 2,000 vp/cell) in the presence of 5 μM NIC or 25 μM OXY and RAF, or the same volume of DMSO for negative control. Forty-five minutes after infection, A549 cells were trypsinized and collected, and then washed twice with PBS. Then, nuclear and cytoplasmic fractions were separated using a hypotonic buffer solution consisting of 20 mM Tris-HCl pH 7.4, 10 mM NaCl, and 3 mM MgCl 2 .

The cell pellet was resuspended in 500 μL of 1 × hypotonic buffer and incubated for 15 min at 4 °C. Then, 25 μL of NP-40 was added and the samples were vortexed. The homogenates were then centrifuged for 10 min at 835 g at 4 °C. HAdV DNA was isolated from the nuclear (pellet) and the cytoplasmic fractions (supernatant) using the QIAamp DNA Mini Kit (QIAGEN, Valencia, CA).

To measure endosome disruption, HAdV-mediated ribotoxin (α-sarcin) delivery assays were performed as previously described 51 HAdV DNA and mRNA quantification by real-time PCR. For DNA quantification, 150,000 A549 cells/ well in a 24-well plate were infected with 100 vp/cell (wild-type HAdV5) and incubated for 2 h at 37 °C in complete DMEM. Then, the excess of virus was washed-out, and the medium was replaced with 500 μL of complete DMEM containing 50 μM of either anthelmintic drugs or the same volume of DMSO (negative control). All samples were done in triplicate. After 24 h of incubation at 37 °C and 5% CO 2 , DNA was purified from the cell lysate using the QIAamp DNA Mini Kit (QIAGEN, Valencia, CA) following the manufacturer's instructions. TaqMan primers, probes and PCR conditions were like those previously reported 51 .

For the evaluation of RNA expression, same conditions of infection applied for the DNA quantification were used. Six hours after infection, RNA was purified with the miRCURY RNA Isolation Kit (Exiqon Inc., MA) following the manufacturer's instructions. Quantification of RNA copy numbers was performed using primers in conditions previously reported for E1A 52 .

Human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was used as internal control. Primers, probes and conditions applied for GAPDH were those previously reported by Rivera et al. 52 . For quantification, gene fragments of hexon and GAPDH were cloned into the pGEM-T Easy vector (Promega), and known concentrations of those vectors were used to generate a standard curve for each experiment. All assays were performed in a C1000 thermal cycler apparatus (BioRad).

A burst assay was used to assay the effect of the three anthelmintic drugs on virus production. A549 cells were infected with wild-type HAdV5, wild-type HAdV16 or wild-type HAdV19 in the presence or absence of 5 μM NIC or 25 μM OXY and RAF. After incubation for 48 h, cells were harvested and subjected to three rounds of freeze/thaw. Then, serial dilutions of clarified lysates were titrated on A549 cells, and TCID 50 values were calculated using a previously reported end-point dilution method 53 .

To test the anti-HCMV activity of these anthelmintic drugs, MRC-5 cells were seeded in a 6-well plate (1.75 × 10 5 cells/well), infected with HCMV (MOI of 0.05 vp/ cell) and incubated in complete DMEM in the presence of 5 μM NIC or 25 μM in case of OXY and RAF or the same volume of DMSO in triplicate. Then, cells were incubated for 72 h at 37 °C and 5% CO 2 and HCMV DNA was purified from the cell lysate using the QIAamp DNA Mini Kit (Qiagen, Valencia, CA) following the manufacturer's instructions. Real-time PCR primers, mixtures and protocols were the same as previously reported 25 . Statistical Analyses. Statistical analyses were carried out using the GraphPad Prism 6 suite. Data are presented as the mean of triplicate samples ± standard deviation (SD), unless otherwise indicated. P < 0.05 was considered statistically significant.

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Supported by Plan Nacional de I + D + i 2013-2016 and Instituto de Salud Carlos III, Ministerio de Economía, Industria y Competitividad, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/0009)co-financed by "A way to achieve Europe" ERDF, the Instituto de Salud Carlos III, Proyectos de Investigación en Salud (PI15/00489) and Proyectos de Desarrollo Tecnológico en Salud (DTS17/00130), and the Spanish Adenovirus Network (AdenoNet, BIO2015/68990-REDT). J.S.C. is supported by the "Contract to Access to the Spanish System of Research and Innovation of the Program of R + D + i of the University of Seville" (USE-13901-D) grant.

J.A.M.L. and A.S.G. have made substantial contributions to acquisition and analysis of data, as well as in the preparation of the manuscript. J.B.C. helped with the acquisition of data. J.P. has made substantial contributions to conception, design and interpretation of data. J.S.C. designed and coordinated the work and the preparation of the manuscript.

Supplementary information accompanies this paper at https://doi.org/10.1038/s41598-018-37290-3.

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