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Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research and antiviral discovery are hampered by the lack of a cell-based virus replication system that can be readily adopted without biosafety level 3 (BSL-3) restrictions. Here, the construction of a noninfectious SARS-CoV-2 reporter re...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053989/ https://www.ncbi.nlm.nih.gov/pubmed/33766889 http://dx.doi.org/10.1073/pnas.2025866118 |
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author | He, Xi Quan, Shuo Xu, Min Rodriguez, Silveria Goh, Shih Lin Wei, Jiajie Fridman, Arthur Koeplinger, Kenneth A. Carroll, Steve S. Grobler, Jay A. Espeseth, Amy S. Olsen, David B. Hazuda, Daria J. Wang, Dai |
author_facet | He, Xi Quan, Shuo Xu, Min Rodriguez, Silveria Goh, Shih Lin Wei, Jiajie Fridman, Arthur Koeplinger, Kenneth A. Carroll, Steve S. Grobler, Jay A. Espeseth, Amy S. Olsen, David B. Hazuda, Daria J. Wang, Dai |
author_sort | He, Xi |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research and antiviral discovery are hampered by the lack of a cell-based virus replication system that can be readily adopted without biosafety level 3 (BSL-3) restrictions. Here, the construction of a noninfectious SARS-CoV-2 reporter replicon and its application in deciphering viral replication mechanisms and evaluating SARS-CoV-2 inhibitors are presented. The replicon genome is replication competent but does not produce progeny virions. Its replication can be inhibited by RdRp mutations or by known SARS-CoV-2 antiviral compounds. Using this system, a high-throughput antiviral assay has also been developed. Significant differences in potencies of several SARS-CoV-2 inhibitors in different cell lines were observed, which highlight the challenges of discovering antivirals capable of inhibiting viral replication in vivo and the importance of testing compounds in multiple cell culture models. The generation of a SARS-CoV-2 replicon provides a powerful platform to expand the global research effort to combat COVID-19. |
format | Online Article Text |
id | pubmed-8053989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-80539892021-05-04 Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing He, Xi Quan, Shuo Xu, Min Rodriguez, Silveria Goh, Shih Lin Wei, Jiajie Fridman, Arthur Koeplinger, Kenneth A. Carroll, Steve S. Grobler, Jay A. Espeseth, Amy S. Olsen, David B. Hazuda, Daria J. Wang, Dai Proc Natl Acad Sci U S A Biological Sciences Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) research and antiviral discovery are hampered by the lack of a cell-based virus replication system that can be readily adopted without biosafety level 3 (BSL-3) restrictions. Here, the construction of a noninfectious SARS-CoV-2 reporter replicon and its application in deciphering viral replication mechanisms and evaluating SARS-CoV-2 inhibitors are presented. The replicon genome is replication competent but does not produce progeny virions. Its replication can be inhibited by RdRp mutations or by known SARS-CoV-2 antiviral compounds. Using this system, a high-throughput antiviral assay has also been developed. Significant differences in potencies of several SARS-CoV-2 inhibitors in different cell lines were observed, which highlight the challenges of discovering antivirals capable of inhibiting viral replication in vivo and the importance of testing compounds in multiple cell culture models. The generation of a SARS-CoV-2 replicon provides a powerful platform to expand the global research effort to combat COVID-19. National Academy of Sciences 2021-04-13 2021-03-25 /pmc/articles/PMC8053989/ /pubmed/33766889 http://dx.doi.org/10.1073/pnas.2025866118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences He, Xi Quan, Shuo Xu, Min Rodriguez, Silveria Goh, Shih Lin Wei, Jiajie Fridman, Arthur Koeplinger, Kenneth A. Carroll, Steve S. Grobler, Jay A. Espeseth, Amy S. Olsen, David B. Hazuda, Daria J. Wang, Dai Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title | Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title_full | Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title_fullStr | Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title_full_unstemmed | Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title_short | Generation of SARS-CoV-2 reporter replicon for high-throughput antiviral screening and testing |
title_sort | generation of sars-cov-2 reporter replicon for high-throughput antiviral screening and testing |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053989/ https://www.ncbi.nlm.nih.gov/pubmed/33766889 http://dx.doi.org/10.1073/pnas.2025866118 |
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