Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis
Favipiravir (T-705) is an inhibitor of viral RNA-dependent-RNA-polymerases (RdRp) and clinical trials for the treatment of COVID-19 are ongoing. Here, the authors show that SARS-CoV nsp12 is the fastest known viral RdRp and they provide insights into the mechanism of action of Favipiravir, demonstra...
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Nature Portfolio
2020
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oai:doaj.org-article:6f077279cc5545ac8b6524fe1944a7d72021-12-02T17:23:48ZRapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis10.1038/s41467-020-18463-z2041-1723https://doaj.org/article/6f077279cc5545ac8b6524fe1944a7d72020-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18463-zhttps://doaj.org/toc/2041-1723Favipiravir (T-705) is an inhibitor of viral RNA-dependent-RNA-polymerases (RdRp) and clinical trials for the treatment of COVID-19 are ongoing. Here, the authors show that SARS-CoV nsp12 is the fastest known viral RdRp and they provide insights into the mechanism of action of Favipiravir, demonstrating that its antiviral effect on SARS-CoV-2 is primarily mediated through lethal mutagenesis.Ashleigh ShannonBarbara SeliskoNhung-Thi-Tuyet LeJohanna HuchtingFranck TouretGéraldine PiorkowskiVéronique FattoriniFrançois FerronEtienne DecrolyChris MeierBruno CoutardOlve PeersenBruno CanardNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-9 (2020) |
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Science Q Ashleigh Shannon Barbara Selisko Nhung-Thi-Tuyet Le Johanna Huchting Franck Touret Géraldine Piorkowski Véronique Fattorini François Ferron Etienne Decroly Chris Meier Bruno Coutard Olve Peersen Bruno Canard Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
description |
Favipiravir (T-705) is an inhibitor of viral RNA-dependent-RNA-polymerases (RdRp) and clinical trials for the treatment of COVID-19 are ongoing. Here, the authors show that SARS-CoV nsp12 is the fastest known viral RdRp and they provide insights into the mechanism of action of Favipiravir, demonstrating that its antiviral effect on SARS-CoV-2 is primarily mediated through lethal mutagenesis. |
format |
article |
author |
Ashleigh Shannon Barbara Selisko Nhung-Thi-Tuyet Le Johanna Huchting Franck Touret Géraldine Piorkowski Véronique Fattorini François Ferron Etienne Decroly Chris Meier Bruno Coutard Olve Peersen Bruno Canard |
author_facet |
Ashleigh Shannon Barbara Selisko Nhung-Thi-Tuyet Le Johanna Huchting Franck Touret Géraldine Piorkowski Véronique Fattorini François Ferron Etienne Decroly Chris Meier Bruno Coutard Olve Peersen Bruno Canard |
author_sort |
Ashleigh Shannon |
title |
Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
title_short |
Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
title_full |
Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
title_fullStr |
Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
title_full_unstemmed |
Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis |
title_sort |
rapid incorporation of favipiravir by the fast and permissive viral rna polymerase complex results in sars-cov-2 lethal mutagenesis |
publisher |
Nature Portfolio |
publishDate |
2020 |
url |
https://doaj.org/article/6f077279cc5545ac8b6524fe1944a7d7 |
work_keys_str_mv |
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