tetano
Editor, Senior Moderator
Virology. 2016 Nov 24;501:92-101. doi: 10.1016/j.virol.2016.11.008. [Epub ahead of print]
[h=1]PB2 substitutions V598T/I increase the virulence of H7N9 influenza A virus in mammals.[/h] Hu M[SUP]1[/SUP], Yuan S[SUP]1[/SUP], Zhang K[SUP]1[/SUP], Singh K[SUP]2[/SUP], Ma Q[SUP]3[/SUP], Zhou J[SUP]4[/SUP], Chu H[SUP]5[/SUP], Zheng BJ[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PB2 is one of the subunits of the influenza A virus (IAV) polymerase complex. By bioinformatics analysis we identified PB2 substitutions at positions 389 and 598 among IAV isolates from humans, which might associate with viral pathogenicity. To evaluate the biological significance of these substitutions, PB2-K389R and -V598T/I mutant viruses of avian H7N9 IAVs were generated by reverse genetics. Compared to the wild type, the mutant viruses displayed an enhanced growth capacity in human and mammalian cells. Meanwhile, they presented increased transcription and replication by producing higher levels of viral mRNA, cRNA and vRNA. Minireplicon assays indicated that the polymerase activity was elevated by these substitutions. Notably, the PB2-V598T/I substitutions substantially increased virus replication and virulence in mice. Together, we demonstrated that the substitutions PB2-V598T/I contributed to higher IAV replication and virulence in mammals, which added to the knowledge of IAV virulence determinants and benefited the surveillance of IAVs.
Copyright © 2016 Elsevier Inc. All rights reserved.
[h=4]KEYWORDS:[/h] Influenza A virus; PB2; PB2-K389R; PB2-V598T/I; Virulence
PMID: 27889648 DOI: 10.1016/j.virol.2016.11.008
[PubMed - as supplied by publisher]
[h=1]PB2 substitutions V598T/I increase the virulence of H7N9 influenza A virus in mammals.[/h] Hu M[SUP]1[/SUP], Yuan S[SUP]1[/SUP], Zhang K[SUP]1[/SUP], Singh K[SUP]2[/SUP], Ma Q[SUP]3[/SUP], Zhou J[SUP]4[/SUP], Chu H[SUP]5[/SUP], Zheng BJ[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PB2 is one of the subunits of the influenza A virus (IAV) polymerase complex. By bioinformatics analysis we identified PB2 substitutions at positions 389 and 598 among IAV isolates from humans, which might associate with viral pathogenicity. To evaluate the biological significance of these substitutions, PB2-K389R and -V598T/I mutant viruses of avian H7N9 IAVs were generated by reverse genetics. Compared to the wild type, the mutant viruses displayed an enhanced growth capacity in human and mammalian cells. Meanwhile, they presented increased transcription and replication by producing higher levels of viral mRNA, cRNA and vRNA. Minireplicon assays indicated that the polymerase activity was elevated by these substitutions. Notably, the PB2-V598T/I substitutions substantially increased virus replication and virulence in mice. Together, we demonstrated that the substitutions PB2-V598T/I contributed to higher IAV replication and virulence in mammals, which added to the knowledge of IAV virulence determinants and benefited the surveillance of IAVs.
Copyright © 2016 Elsevier Inc. All rights reserved.
[h=4]KEYWORDS:[/h] Influenza A virus; PB2; PB2-K389R; PB2-V598T/I; Virulence
PMID: 27889648 DOI: 10.1016/j.virol.2016.11.008
[PubMed - as supplied by publisher]