tetano
Editor, Senior Moderator
J Gen Virol
. 2021 Oct;102(10).
doi: 10.1099/jgv.0.001659.
Replication and transmission of an influenza A(H3N2) virus harboring the polymerase acidic I38T substitution, in guinea pigs
Zeineb Mhamdi[SUP] 1 [/SUP], Julie Carbonneau[SUP] 1 [/SUP], Marie-Christine Venable[SUP] 1 [/SUP], Mariana Baz[SUP] 1 [/SUP], Yacine Abed[SUP] 1 [/SUP], Guy Boivin[SUP] 1 [/SUP]
Affiliations
Abstract
The polymerase acidic (PA) I38T substitution is a dominant marker of resistance to baloxavir. We evaluated the impact of I38T on the fitness of a contemporary influenza A(H3N2) virus. Influenza A/Switzerland/9715293/2013 (H3N2) wild-type (WT) virus and its I38T mutant were rescued by reverse genetics. Replication kinetics were compared using ST6GalI-MDCK and A549 cells and infectivity/contact transmissibility were evaluated in guinea pigs. Nasal wash (NW) viral titres were determined by TCID50 ml[SUP]-1[/SUP] in ST6GalI-MDCK cells. Competition experiments were performed and the evolution of viral population was assessed by droplet digital RT-PCR. I38T did not alter in vitro replication. I38T induced comparable titres vs the WT in guinea pigs NWs and the two viruses transmitted equally by direct contact. However, a 50 %:50 % mixture inoculum evolved to mean WT/I38T ratios of 71 %:29 % and 66.4 %:33.6 % on days 4 and 6 p.i., respectively. Contemporary influenza A(H3N2)-I38T PA variants may conserve a significant level of viral fitness.
Keywords: H3N2; I38T; Influenza; baloxavir; fitness; guinea pigs; marboxil.
. 2021 Oct;102(10).
doi: 10.1099/jgv.0.001659.
Replication and transmission of an influenza A(H3N2) virus harboring the polymerase acidic I38T substitution, in guinea pigs
Zeineb Mhamdi[SUP] 1 [/SUP], Julie Carbonneau[SUP] 1 [/SUP], Marie-Christine Venable[SUP] 1 [/SUP], Mariana Baz[SUP] 1 [/SUP], Yacine Abed[SUP] 1 [/SUP], Guy Boivin[SUP] 1 [/SUP]
Affiliations
- PMID: 34661516
- DOI: 10.1099/jgv.0.001659
Abstract
The polymerase acidic (PA) I38T substitution is a dominant marker of resistance to baloxavir. We evaluated the impact of I38T on the fitness of a contemporary influenza A(H3N2) virus. Influenza A/Switzerland/9715293/2013 (H3N2) wild-type (WT) virus and its I38T mutant were rescued by reverse genetics. Replication kinetics were compared using ST6GalI-MDCK and A549 cells and infectivity/contact transmissibility were evaluated in guinea pigs. Nasal wash (NW) viral titres were determined by TCID50 ml[SUP]-1[/SUP] in ST6GalI-MDCK cells. Competition experiments were performed and the evolution of viral population was assessed by droplet digital RT-PCR. I38T did not alter in vitro replication. I38T induced comparable titres vs the WT in guinea pigs NWs and the two viruses transmitted equally by direct contact. However, a 50 %:50 % mixture inoculum evolved to mean WT/I38T ratios of 71 %:29 % and 66.4 %:33.6 % on days 4 and 6 p.i., respectively. Contemporary influenza A(H3N2)-I38T PA variants may conserve a significant level of viral fitness.
Keywords: H3N2; I38T; Influenza; baloxavir; fitness; guinea pigs; marboxil.