TY - JOUR
T1 - Murine norovirus (MNV-1) exposure in vitro to the purine nucleoside analog Ribavirin increases quasispecies diversity
AU - Julian, Timothy R.
AU - Baugher, Joseph D.
AU - Rippinger, Christine M.
AU - Pinekenstein, Rebecca
AU - Kolawole, Abimbola O.
AU - Mehoke, Thomas S.
AU - Wobus, Christiane E.
AU - Feldman, Andrew B.
AU - Pineda, Fernando J.
AU - Schwab, Kellogg J.
N1 - Funding Information:
This work was supported by the Defense Advanced Research Projects Agency (DARPA) Contract HR0011-11-C-0093 and The Johns Hopkins Water Institute. We would like to thank J. Max Trumble, and Jason Bishai for technical laboratory support.
Publisher Copyright:
© 2015 Elsevier B.V..
PY - 2016/1/4
Y1 - 2016/1/4
N2 - Ribavirin is a pharmaceutical antiviral used for the treatment of RNA virus infections including norovirus, hepatitis C virus, hepatitis E virus, Lassa virus, respiratory syncytial virus, and rhinovirus. Despite the drug's history and documented efficacy, the antiviral mechanism of Ribavirin remains unclear. Mechanisms proposed include depletion of the intracellular GTP pool, immunomodulatory effects, induction of error catastrophe, inhibition of viral polymerase activity, and/or inhibition of viral capping. In the present study, we leveraged deep sequencing data to demonstrate that Ribavirin increases murine norovirus (MNV-1) viral diversity. By serial passaging MNV-1 in RAW 264.7 cells for twenty generations in the presence of Ribavirin, we demonstrated statistically significant increases in both the number of unique haplotypes and the average pairwise difference (APD). Based on statistically significant differences in the probability of nucleotide mutations based on Roche 454 sequencing, we also demonstrated that single nucleotide substitutions are increased in the presence of Ribavirin. Finally, we demonstrated Ribavirin's impact on statistically significantly reducing the relative proportion of the dominant sequence within the quasispecies.
AB - Ribavirin is a pharmaceutical antiviral used for the treatment of RNA virus infections including norovirus, hepatitis C virus, hepatitis E virus, Lassa virus, respiratory syncytial virus, and rhinovirus. Despite the drug's history and documented efficacy, the antiviral mechanism of Ribavirin remains unclear. Mechanisms proposed include depletion of the intracellular GTP pool, immunomodulatory effects, induction of error catastrophe, inhibition of viral polymerase activity, and/or inhibition of viral capping. In the present study, we leveraged deep sequencing data to demonstrate that Ribavirin increases murine norovirus (MNV-1) viral diversity. By serial passaging MNV-1 in RAW 264.7 cells for twenty generations in the presence of Ribavirin, we demonstrated statistically significant increases in both the number of unique haplotypes and the average pairwise difference (APD). Based on statistically significant differences in the probability of nucleotide mutations based on Roche 454 sequencing, we also demonstrated that single nucleotide substitutions are increased in the presence of Ribavirin. Finally, we demonstrated Ribavirin's impact on statistically significantly reducing the relative proportion of the dominant sequence within the quasispecies.
KW - MNV-1
KW - Norovirus
KW - Quasispecies
KW - Ribavirin
KW - Serial passaging
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U2 - 10.1016/j.virusres.2015.10.016
DO - 10.1016/j.virusres.2015.10.016
M3 - Article
C2 - 26494169
AN - SCOPUS:84951849369
SN - 0168-1702
VL - 211
SP - 165
EP - 173
JO - Virus Research
JF - Virus Research
ER -