tetano
Editor, Senior Moderator
Int J Mol Sci. 2017 Dec 29;19(1). pii: E96. doi: 10.3390/ijms19010096.
[h=1]Evolution and Virulence of Influenza A Virus Protein PB1-F2.[/h] Kamal RP[SUP]1,[/SUP][SUP]2[/SUP], Alymova IV[SUP]3[/SUP], York IA[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PB1-F2 is an accessory protein of most human, avian, swine, equine, and canine influenza A viruses (IAVs). Although it is dispensable for virus replication and growth, it plays significant roles in pathogenesis by interfering with the host innate immune response, inducing death in immune and epithelial cells, altering inflammatory responses, and promoting secondary bacterial pneumonia. The effects of PB1-F2 differ between virus strains and host species. This can at least partially be explained by the presence of multiple PB1-F2 sequence variants, including premature stop codons that lead to the expression of truncated PB1-F2 proteins of different lengths and specific virulence-associated residues that enhance susceptibility to bacterial superinfection. Although there has been a tendency for human seasonal IAV to gradually reduce the number of virulence-associated residues, zoonotic IAVs contain a reservoir of PB1-F2 proteins with full length, virulence-associated sequences. Here, we review the molecular mechanisms by which PB1-F2 may affect influenza virulence, and factors associated with the evolution and selection of this protein.
[h=4]KEYWORDS:[/h] PB1-F2; influenza; pathogenesis; virulence
PMID: 29286299 DOI: 10.3390/ijms19010096
[h=1]Evolution and Virulence of Influenza A Virus Protein PB1-F2.[/h] Kamal RP[SUP]1,[/SUP][SUP]2[/SUP], Alymova IV[SUP]3[/SUP], York IA[SUP]4[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] PB1-F2 is an accessory protein of most human, avian, swine, equine, and canine influenza A viruses (IAVs). Although it is dispensable for virus replication and growth, it plays significant roles in pathogenesis by interfering with the host innate immune response, inducing death in immune and epithelial cells, altering inflammatory responses, and promoting secondary bacterial pneumonia. The effects of PB1-F2 differ between virus strains and host species. This can at least partially be explained by the presence of multiple PB1-F2 sequence variants, including premature stop codons that lead to the expression of truncated PB1-F2 proteins of different lengths and specific virulence-associated residues that enhance susceptibility to bacterial superinfection. Although there has been a tendency for human seasonal IAV to gradually reduce the number of virulence-associated residues, zoonotic IAVs contain a reservoir of PB1-F2 proteins with full length, virulence-associated sequences. Here, we review the molecular mechanisms by which PB1-F2 may affect influenza virulence, and factors associated with the evolution and selection of this protein.
[h=4]KEYWORDS:[/h] PB1-F2; influenza; pathogenesis; virulence
PMID: 29286299 DOI: 10.3390/ijms19010096