| Literature DB >> 31541547 |
Anton Chesnokov1,2, Mira C Patel1,3, Vasiliy P Mishin1, Juan A De La Cruz1,3, Lori Lollis1,3, Ha T Nguyen1,3, Vivien Dugan1, David E Wentworth1, Larisa V Gubareva1.
Abstract
Susceptibility of influenza A viruses to baloxavir can be affected by changes at amino acid residue 38 in the polymerase acidic (PA) protein. Information on replicative fitness of PA-I38-substituted viruses remains sparse. We demonstrated that substitutions I38L/M/S/T not only had a differential effect on baloxavir susceptibility (9- to 116-fold) but also on in vitro replicative fitness. Although I38L conferred undiminished growth, other substitutions led to mild attenuation. In a ferret model, control viruses outcompeted those carrying I38M or I38T substitutions, although their advantage was limited. These findings offer insights into the attributes of baloxavir-resistant viruses needed for informed risk assessment. Published by Oxford University Press for the Infectious Diseases Society of America 2019.Entities:
Keywords: baloxavir acid; drug resistance; ferret; influenza; polymerase acidic protein
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Year: 2020 PMID: 31541547 PMCID: PMC8851376 DOI: 10.1093/infdis/jiz472
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226