key: cord-0979544-b9na3yf6 authors: Yong, Suh Kuan; Su, Ping‐Chia; Yang, Yuh‐Shyong title: Molecular Targets for the Testing of COVID‐19 date: 2020-05-18 journal: Biotechnol J DOI: 10.1002/biot.202000152 sha: 828947e95ae780f8484d60720d05e3049baa95df doc_id: 979544 cord_uid: b9na3yf6 The pandemic outbreaks of coronavirus disease 2019 (COVID‐19), caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), spread all over the world in a short period of time. Efficient identification of the infection by SARS‐CoV‐2 has been one of the most important tasks to facilitate all the following counter measurements in dealing with the infectious disease. In Taiwan, a COVID‐19 Open Science Platform adheres to the spirit of open science: sharing sources, data, and methods to promote progress in academic research while corroborating findings from various disciplines has established in mid‐February 2020, for collaborative research in support of the development of detection methods, therapeutics, and a vaccine for COVID‐19. Research priorities include infection control, epidemiology, clinical characterization and management, detection methods (including viral RNA detection, viral antigen detection, and serum antibody detection), therapeutics (neutralizing antibody and small molecule drugs), vaccines, and SARS‐CoV‐2 pathogenesis. In addition, research on social ethics and the law are included to take full account of the impact of the COVID‐19 virus. The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/biot.202000152 DOI: 10.1002/biot.202000152 structure that composes four types of protein, such as spike glycoprotein (S), envelope protein (E), membrane protein (M), and nucleocapsid protein (N). The S protein is playing an important role in invading into the host, by interacting with human receptor angiotensin-converting enzyme 2 (ACE2). The receptor-binding domain (RBD) of S protein contributed its immunogenic that attracted many neutralizing antibodies. [5, 6] They are all potential molecular targets for the identification of SARS-CoV-2 infection. Currently, there is no specific therapeutic drug or vaccine for COVID-19; therefore, it is necessary to deploy a robust diagnostic methodology which is rapid, accurate, and ultrasensitive to isolate infected patients from the healthy population. The testing of SARS-CoV-2 is grouped into molecular testing and serology testing. The molecular testing includes nucleic acid amplification test (NAAT) such as real-time reverse-transcription polymerase chain reaction (rRT-PCR). [7] According to World Health Organization (WHO) interim guidance on laboratory testing of COVID-19 in suspected human, [7] the respiratory materials were required to collect to perform NAAT. The unique sequence RNA of the virus including nucleocapsid (N), envelope (E), spike protein (S), and RNA-dependent RNA-polymerase (RdRP) genes are targeted to analyze using rRT-PCR. [8] On January 23, 2020, the first COVID-19 detection kit using rRT-PCR was published which targeted RdRP, N, and E genes of SARS-CoV-2. [8] As of now, there are many in-house or commercial COVID-19 molecular assays available from worldwide, for instance, 1) "CDC 2019-nCoV real-time reverse transcriptase PCR diagnostic panel" was developed by the United States Centers for Disease Control and Prevention. This diagnostic panel is working with Applied Biosystems 7500 Fast DX Real-Time PCR Instrument with SDS 1.4 software; 2) "New coronavirus nucleic acid assay" which targeted on ORF1ab and N genes was developed by Chinese National Institute for Viral Disease Control and Prevention; 3) Molecular test kits from four companies such as Seegene Inc., Kogene Biotech Co. Ltd., Sd Biosensor Inc., and Solgent Co. were approved by Ministry Food and Drug Safety and Korea Centers for Disease Control and Prevention which are now widely being used in South Korea. [9] Primer and probe design are critical for the detection of or viral RNA that is easy to mutate. Taiwan Centers for Disease Control provides rRT-PCR primers targeting www.advancedsciencenews.com www.biotechnology-journal.com E, RdRp, and N genes for first-line screening, confirmatory, and additional confirmatory assay, respectively. The outbreaks of the COVID-19 pandemic have led to an increase of thousands of active cases every day all over the world, and we are racing against time to find a test to quickly detect the virus and isolate the infected patient from healthy population to stop the virus transmission from a further outbreak. The United States Food and Drug Administration is moving fast to approve a few COVID-19 molecular test kits under Emergency Use Authorization powers. Cepheid Inc., Mesa Biotech Inc., and BioFire Defense LLC were recently granted Food and Drug Administration (FDA) approval of their rapid diagnostic test that could give the test result reduced to 1 h compared to traditional RT-PCR methods that required 3-4 h. On March 27, 2020, Abbott announced the launch of a molecular point-of-care test, which uses an isothermal RNA amplification method to deliver positive results in 5 min and negative results in 13 min. It is expected to produce about 5 million tests per month (https://www.abbott.com/corpnewsroom/productand-innovation/detect-covid-19-in-as-little-as-5-minutes.html). In addition to its RNA, the S and the N proteins are frequent targets for the detection of conorovirus. In contrast to that of the RNA, the development of a detection kit on viral proteins is still in progress. A probe, usually a specific antibody, is needed before a successful viral protein detection method can be developed. In early March 2020, Academia Sinica, Taiwan, reported the first monoclonal antibody against N protein of Sars-CoV-2. With their antibody library in hand, the team screened against N proteins from seven different viral species to obtain 1 antibody against only SARS-CoV-2 N protein, 9 against only SARS-CoV N protein, and 36 against both SARS-CoV-2 and SARS-CoV N proteins. [10] The results indicated that rapid immune-based test kit of SARS-CoV-2 coronavirus can be developed in the future. It also shows the complexity and time consumed in obtaining and screening an antibody for an unbiased test targeting specific viral protein. The procedure for the preparation of specific antibody from laboratory animal has been very well established and it could be expected that numerous antibodies specific for a SARS-CoV-2 protein will be reported soon. 25 strains of antibodies from three COVID-19 patients have also been prepared from Chang Gung Memorial Hospital, Taiwan. There are 13 strains of monoclonal antibodies (mAbs) targeting on S protein, and 12 strains of mAbs targeting on N protein of the SARS-CoV-2. These antibodies, especially those targeting on S protein, can be a potential probe for the detection of S protein or the whole SARS-CoV-2 virus. The advantage of immune-based vial detection is its simplicity and speed (within 15 min). However, the antibodies prepared from SARS-CoV-2 protein antigen may cross-react with proteins from other similar viruses such as SARS-CoV and MERS, and thus a tedious screening procedure is needed before a specific testing kit can be developed. As aforementioned, the serology testing of COVID-19 is not targeting the virus itself but the antibodies such as immunoglobulin M (IgM) and immunoglobulin G (IgG) induced following viral infection. These immunoglobulins were serological testing markers for after the patient has early (3-6 days after exposure to the virus, IgM) and late virus infections (after 8 days, IgG) response respectively. [11] The serological testing is crucial to identify active patients, asymptomatic carriers or convalescent persons, and provide population surveillance. These data could be used to analyze and estimate the SARS-CoV-2 epidemiology and virology [12] and help to contain the outbreak of the pandemic. The highly reactive human could be the donor of convalescent serum for therapeutic. [13] The WHO interim guidance on COVID-19 www.advancedsciencenews.com www.biotechnology-journal.com testing suggested collecting blood, stool, or autopsy materials such as lungs (deceased patients) as serology testing specimens. [7] As it has been reported that several factors could contribute to a high false-negative rate when using NAAT, serology testing should also be taken into consideration as alternative testing or correlation testing. [14] There are companies such as Guangzhou Wondfo Biotech, China; Innovita Biological Technology, China; Pharma (Berlin), Germany; and RayBiotech Inc., USA, that have released various types of test kits that specifically test on COVID-19 IgM and IgG. Specificity and sensitivity are two fundamental requirements for an effective diagnosis. It is also important that the testing method is user friendly. RNA detection is the most frequently used method for the identification of COVID-19 patients because this method is extremely sensitive due to the power of nucleic acid amplification and also highly specific by using complementary nucleic acid probe/primer for the identification of a particular RNA. The major drawback in such an emergency situation is probably the requirement of well-trained personnel and lengthy testing time (usually 3-4 h) to run the test. However, it has been announced that positive/negative COVID-19 can be determined in about 10 min by using the isothermal amplification method. This may due to the simplification of the NAAT procedure and the high amount of the SARS-CoV-2 at the beginning of the infection to be detected. Detections on viral proteins, such as S and N proteins, give complementary information to that of RNA detection from the same sample. This method is more direct (without amplification), but is less sensitive. It needs more effort to obtain a suitable probe (usually antibody), but the testing method can be simple. Recent developments in biosensing technologies can significantly improve the protein sensing sensitivity, such as the use of magnetic bead to concentrate the protein molecules or by applying nanowire field-effect transistor as a transducer. Many of the entrepreneurs may take this opportunity to fasten their product development. Serology testings targeting on viral-induced antibodies are given different information as those for viral RNA and proteins from SARS-CoV-2. Although the protein testing method is similar, the targets are not part of the virus and the testing specimens used can be quite different as compared to those for viral protein detection. It is unfortunate that the world is currently suffering from the COVID-19 epidemic. However, we should expect that such an incident would reappear. We wish that the world would be better prepared every time we face a potential spread of an infectious disease. Biosensing technologies have progressed rapidly in the past decade. The pandemic outbreaks of COVID-19 continue to remind us that diagnostic tools are critical and needed to be prepared in advance. Suh Kuan Yong, Ping-Chia Su and Yuh-Shyong Yang World Health Organization, Coronavirus disease 2019 (COVID-19) Situation Report World Health Organization, Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases: Interim World Health Organization, Coronavirus disease 2019 (COVID-19) Situation Report Proceedings of the National Academy of Sciences 2020 This work was supported by the Ministry of Science and Technology, Taiwan (Grant No: 108-2218-E-009-003). The authors declare no conflict of interest.Keywords coronavirus, COVID-19, molecular testing, rapid-diagnostic test (RDT), SARS-CoV-2, serology testing