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Maraviroc inhibits SARS-CoV-2 multiplication and s-protein mediated cell fusion in cell culture
Kenneth Risner; Katie V Tieu; Yafei Wang; Michael Getz; Allison Bakovic; Nishank Bhalla; Steven Nathan; Daniel E Conway; Paul Macklin; Aarthi Narayanan.
Afiliação
  • Kenneth Risner; George Mason University
  • Katie V Tieu; Virginia Commonwealth University
  • Yafei Wang; Indiana University
  • Michael Getz; Indiana University
  • Allison Bakovic; George Mason University
  • Nishank Bhalla; George Mason University
  • Steven Nathan; INOVA Fairfax Hospital
  • Daniel E Conway; Virginia Commonwealth University
  • Paul Macklin; Indiana University
  • Aarthi Narayanan; George Mason University
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-246389
ABSTRACT
In an effort to identify therapeutic intervention strategies for the treatment of COVID-19, we have investigated a selection of FDA-approved small molecules and biologics that are commonly used to treat other human diseases. A investigation into 18 small molecules and 3 biologics was conducted in cell culture and the impact of treatment on viral titer was quantified by plaque assay. The investigation identified 4 FDA-approved small molecules, Maraviroc, FTY720 (Fingolimod), Atorvastatin and Nitazoxanide that were able to inhibit SARS-CoV-2 infection. Confocal microscopy with over expressed S-protein demonstrated that Maraviroc reduced the extent of S-protein mediated cell fusion as observed by fewer multinucleate cells in the context of drugtreatment. Mathematical modeling of drug-dependent viral multiplication dynamics revealed that prolonged drug treatment will exert an exponential decrease in viral load in a multicellular/tissue environment. Taken together, the data demonstrate that Maraviroc, Fingolimod, Atorvastatin and Nitazoxanide inhibit SARS-CoV-2 in cell culture.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
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