Molnupiravir inhibits SARS-CoV-2 variants including Omicron in the hamster model

  • JCI Insight. 2022 Jul 8;7(13):e160108. doi: 10.1172/jci.insight.160108.
Kyle Rosenke  1 Atsushi Okumura  1 Matthew C Lewis  1 Friederike Feldmann  2 Kimberly Meade-White  1 W Forrest Bohler  1 Amanda Griffin  1 Rebecca Rosenke  2 Carl Shaia  2 Michael A Jarvis  1  3  4 Heinz Feldmann  1
Affiliations
  • 1. Laboratory of Virology and.
  • 2. Rocky Mountain Veterinary Branch, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Hamilton, Montana, USA.
  • 3. School of Biomedical Sciences, University of Plymouth, Plymouth, United Kingdom.
  • 4. The Vaccine Group, Plymouth, United Kingdom.
Abstract

The recent emergence of the SARS-CoV-2 Omicron variant of concern (VOC), which contains a heavily mutated spike protein capable of escaping preexisting immunity, identifies a continued need for interventional measures. Molnupiravir (MK-4482), an orally administered nucleoside analog, has demonstrated efficacy against earlier SARS-CoV-2 lineages and was recently approved for SARS-CoV-2 infections in high-risk adults. Here, we assessed the efficacy of MK-4482 against the earlier Alpha, Beta, and Delta VOCs and Omicron in the hamster COVID-19 model. Omicron replication and associated lung disease in vehicle-treated hamsters was reduced compared with replication and lung disease associated with earlier VOCs. MK-4482 treatment inhibited virus replication in the lungs of hamsters infected with Alpha, Beta, or Delta VOCs. Importantly, MK-4482 profoundly inhibited virus replication in the upper and lower respiratory tract of hamsters infected with the Omicron VOC. Consistent with its mutagenic mechanism, MK-4482 treatment had a more pronounced inhibitory effect on infectious titers compared with viral RNA genome load. Histopathologic analysis showed that MK-4482 treatment caused a concomitant reduction in the level of lung disease and viral antigen load in infected hamsters across all VOCs examined. Together, our data indicate the potential of MK-4482 as an effective Antiviral against known SARS-CoV-2 VOCs, especially Omicron, and likely future SARS-CoV-2 variants.

Keywords
COVID-19; Drug therapy; Mouse models; Virology.
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