tetano
Editor, Senior Moderator
PLoS One. 2017 Apr 14;12(4):e0175655. doi: 10.1371/journal.pone.0175655. eCollection 2017.
[h=1]Evolution of the neuraminidase gene of seasonal influenza A and B viruses in Thailand between 2010 and 2015.[/h] Tewawong N[SUP]1[/SUP], Vichiwattana P[SUP]1[/SUP], Korkong S[SUP]1[/SUP], Klinfueng S[SUP]1[/SUP], Suntronwong N[SUP]1[/SUP], Thongmee T[SUP]1[/SUP], Theamboonlers A[SUP]1[/SUP], Vongpunsawad S[SUP]1[/SUP], Poovorawan Y[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The neuraminidase inhibitors (NAIs) oseltamivir and zanamivir are commonly used for the treatment and control of influenza A and B virus infection. However, the emergence of new influenza virus strains with reduced susceptibility to NAIs may appear with the use of these antivirals or even naturally. We therefore screened the neuraminidase (NA) sequences of seasonal influenza virus A(H1N1), A(H1N1)pdm09, A(H3N2), and influenza B virus strains identified in Thailand for the presence of substitutions previously reported to reduce susceptibility to NAIs. We initially examined oseltamivir resistance (characterized by the H275Y mutation in the NA gene) in 485 A(H1N1)pdm09 strains circulating in Thailand and found that 0.82% (4/485) had this substitution. To further evaluate the evolution of the NA gene, we also randomly selected 98 A(H1N1)pdm09, 158 A(H3N2), and 69 influenza B virus strains for NA gene amplification and sequencing, which revealed various amino acid mutations in the active site of the NA protein previously shown to be associated with reduced susceptibility to NAIs. Phylogenetic analysis of the influenza virus strains from this study and elsewhere around the world, together with the estimations of nucleotide substitution rates and selection pressure, and the predictions of B-cell epitopes and N-linked glycosylation sites all provided evidence for the ongoing evolution of NA. The overall rates of NA evolution for influenza A viruses were higher than for influenza B virus at the nucleotide level, although influenza B virus possessed more genealogical diversity than that of influenza A viruses. The continual surveillance of the antigenic changes associated with the NA protein will not only contribute to the influenza virus database but may also provide a better understanding of selection pressure exerted by antiviral use.
PMID: 28410396 DOI: 10.1371/journal.pone.0175655
[h=1]Evolution of the neuraminidase gene of seasonal influenza A and B viruses in Thailand between 2010 and 2015.[/h] Tewawong N[SUP]1[/SUP], Vichiwattana P[SUP]1[/SUP], Korkong S[SUP]1[/SUP], Klinfueng S[SUP]1[/SUP], Suntronwong N[SUP]1[/SUP], Thongmee T[SUP]1[/SUP], Theamboonlers A[SUP]1[/SUP], Vongpunsawad S[SUP]1[/SUP], Poovorawan Y[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The neuraminidase inhibitors (NAIs) oseltamivir and zanamivir are commonly used for the treatment and control of influenza A and B virus infection. However, the emergence of new influenza virus strains with reduced susceptibility to NAIs may appear with the use of these antivirals or even naturally. We therefore screened the neuraminidase (NA) sequences of seasonal influenza virus A(H1N1), A(H1N1)pdm09, A(H3N2), and influenza B virus strains identified in Thailand for the presence of substitutions previously reported to reduce susceptibility to NAIs. We initially examined oseltamivir resistance (characterized by the H275Y mutation in the NA gene) in 485 A(H1N1)pdm09 strains circulating in Thailand and found that 0.82% (4/485) had this substitution. To further evaluate the evolution of the NA gene, we also randomly selected 98 A(H1N1)pdm09, 158 A(H3N2), and 69 influenza B virus strains for NA gene amplification and sequencing, which revealed various amino acid mutations in the active site of the NA protein previously shown to be associated with reduced susceptibility to NAIs. Phylogenetic analysis of the influenza virus strains from this study and elsewhere around the world, together with the estimations of nucleotide substitution rates and selection pressure, and the predictions of B-cell epitopes and N-linked glycosylation sites all provided evidence for the ongoing evolution of NA. The overall rates of NA evolution for influenza A viruses were higher than for influenza B virus at the nucleotide level, although influenza B virus possessed more genealogical diversity than that of influenza A viruses. The continual surveillance of the antigenic changes associated with the NA protein will not only contribute to the influenza virus database but may also provide a better understanding of selection pressure exerted by antiviral use.
PMID: 28410396 DOI: 10.1371/journal.pone.0175655