Nature Communications (Sep 2020)

Rapid incorporation of Favipiravir by the fast and permissive viral RNA polymerase complex results in SARS-CoV-2 lethal mutagenesis

  • 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

DOI
https://doi.org/10.1038/s41467-020-18463-z
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 9

Abstract

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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.