Characterization of susceptibility variants of poliovirus grown in the presence of favipiravir.

J Microbiol Immunol Infect

Department of Virology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan. Electronic address:

Published: October 2018

AI Article Synopsis

  • T-705 (favipiravir) effectively inhibits RNA-dependent RNA polymerases in influenza viruses and has not shown any signs of developing resistance.
  • In a study with poliovirus I (Sabin strain), variants resistant to favipiravir were isolated and analyzed for susceptibility and RNA polymerase mutations.
  • The findings suggest that favipiravir acts as a chain terminator, preventing the lethal mutagenesis seen with ribavirin, and although some mutations occurred, they were detrimental to the virus's RNA polymerase function.

Article Abstract

Background: T-705 (favipiravir) is a potent inhibitor of RNA-dependent RNA polymerases of influenza viruses and no favipiravir-resistant virus has been isolated. Poliovirus RNA polymerase has been well characterized and isolation of resistant virus was examined in poliovirus.

Methods: Susceptibility variants of poliovirus I (Sabin strain) were isolated during passages in the presence of favipiravir and characterized for their susceptibility and the sequence of RNA polymerase.

Results: Five variants with 0.47-1.88 times the 50% inhibitory concentration for plaque formation of the parent poliovirus had amino acid variations in the 3D gene of the RNA polymerase. The distribution of amino acid variations was not related to ribavirin resistance, and two amino acid variation sites were found near the finger domain.

Conclusion: Favipiravir as a chain terminator would not be incorporated and replicate to cause lethal mutagenesis as a mutagen like ribavirin, and resistant mutants were not isolated. A high replication level would generate mutations leading to favipiravir resistance as ribavirin resistance was generated, but generated mutations would be lethal to the RNA polymerase function.

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Source
http://dx.doi.org/10.1016/j.jmii.2017.03.004DOI Listing

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