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Remdesivir Metabolite GS-441524 Efficiently Inhibits SARS-CoV-2 Infection in Mouse Model
Yingjun Li; Liu Cao; Ge Li; Feng Cong; Yunfeng Li; Jing Sun; Yinzhu Luo; Guijiang Chen; Guanguan Li; Ping Wang; Fan Xing; Yanxi Ji; Jincun Zhao; Yu Zhang; Deyin Guo; Xumu Zhang.
Afiliación
  • Yingjun Li; Southern University of Science and Technology
  • Liu Cao; Sun Yat-sen University
  • Ge Li; Guangdong Laboratory Animals Monitoring Institute
  • Feng Cong; Guangdong Laboratory Animals Monitoring Institute
  • Yunfeng Li; Guangdong Laboratory Animals Monitoring Institute
  • Jing Sun; National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention
  • Yinzhu Luo; Guangdong Laboratory Animals Monitoring Institute
  • Guijiang Chen; Guangdong Laboratory Animals Monitoring Institute
  • Guanguan Li; Southern University of Science and Technology
  • Ping Wang; Southern University of Science and Technology
  • Fan Xing; Sun Yat-sen University
  • Yanxi Ji; Sun Yat-sen University
  • Jincun Zhao; GIRH
  • Yu Zhang; Guangdong Laboratory Animals Monitoring Institute
  • Deyin Guo; Sun Yat-sen University
  • Xumu Zhang; Southern University of Science and Technology
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-353300
ABSTRACT
The outbreak of coronavirus disease 2019 (COVID-19) rapidly spreads across worldwide and becomes a global pandemic. Remdesivir is the only COVID-19 treatment approved by U.S. Food and Drug Administration (FDA); however, its effectiveness is still under questioning as raised by the results of a large WHO Solidarity Trial. Herein, we report that the parent nucleotide of remdesivir, GS-441524, potently inhibits the replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in Vero E6 and other cells. It exhibits good plasma distribution and longer half-life (t1/2=4.8h) in rat PK study. GS-441524 is highly efficacious against SARS-CoV-2 in AAV-hACE2 transduced mice and murine hepatitis virus (MHV) in mice, reducing the viral titers in CoV-attacked organs, without noticeable toxicity. Given that GS-441524 was the predominant metabolite of remdesivir in the plasma, the anti-COVID-19 effect of remdesivir may partly come from the effect of GS-441524. Our results also supported that GS-441524 as a promising and inexpensive drug candidate in the treatment of COVID-19 and future emerging CoVs diseases.
Licencia
cc_by_nc_nd
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Rct Idioma: En Año: 2020 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Rct Idioma: En Año: 2020 Tipo del documento: Preprint