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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
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.
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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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