tetano
Editor, Senior Moderator
PLoS One. 2015 Oct 6;10(10):e0139958. doi: 10.1371/journal.pone.0139958. eCollection 2015.
[h=1]Assessing Antigenic Drift of Seasonal Influenza A(H3N2) and A(H1N1)pdm09 Viruses.[/h] Tewawong N[SUP]1[/SUP], Prachayangprecha S[SUP]1[/SUP], Vichiwattana P[SUP]1[/SUP], Korkong S[SUP]1[/SUP], Klinfueng S[SUP]1[/SUP], Vongpunsawad S[SUP]1[/SUP], Thongmee T[SUP]1[/SUP], Theamboonlers A[SUP]1[/SUP], Poovorawan Y[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Under selective pressure from the host immune system, antigenic epitopes of influenza virus hemagglutinin (HA) have continually evolved to escape antibody recognition, termed antigenic drift. We analyzed the genomes of influenza A(H3N2) and A(H1N1)pdm09 virus strains circulating in Thailand between 2010 and 2014 and assessed how well the yearly vaccine strains recommended for the southern hemisphere matched them. We amplified and sequenced the HA gene of 120 A(H3N2) and 81 A(H1N1)pdm09 influenza virus samples obtained from respiratory specimens and calculated the perfect-match vaccine efficacy using the pepitope model, which quantitated the antigenic drift in the dominant epitope of HA. Phylogenetic analysis of the A(H3N2) HA1 genes classified most strains into genetic clades 1, 3A, 3B, and 3C. The A(H3N2) strains from the 2013 and 2014 seasons showed very low to moderate vaccine efficacy and demonstrated antigenic drift from epitopes C and A to epitope B. Meanwhile, most A(H1N1)pdm09 strains from the 2012-2014 seasons belonged to genetic clades 6A, 6B, and 6C and displayed the dominant epitope mutations at epitopes B and E. Finally, the vaccine efficacy for A(H1N1)pdm09 (79.6-93.4%) was generally higher than that of A(H3N2). These findings further confirmed the accelerating antigenic drift of the circulating influenza A(H3N2) in recent years.
PMID: 26440103 [PubMed - in process] Free full text
[h=1]Assessing Antigenic Drift of Seasonal Influenza A(H3N2) and A(H1N1)pdm09 Viruses.[/h] Tewawong N[SUP]1[/SUP], Prachayangprecha S[SUP]1[/SUP], Vichiwattana P[SUP]1[/SUP], Korkong S[SUP]1[/SUP], Klinfueng S[SUP]1[/SUP], Vongpunsawad S[SUP]1[/SUP], Thongmee T[SUP]1[/SUP], Theamboonlers A[SUP]1[/SUP], Poovorawan Y[SUP]1[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Under selective pressure from the host immune system, antigenic epitopes of influenza virus hemagglutinin (HA) have continually evolved to escape antibody recognition, termed antigenic drift. We analyzed the genomes of influenza A(H3N2) and A(H1N1)pdm09 virus strains circulating in Thailand between 2010 and 2014 and assessed how well the yearly vaccine strains recommended for the southern hemisphere matched them. We amplified and sequenced the HA gene of 120 A(H3N2) and 81 A(H1N1)pdm09 influenza virus samples obtained from respiratory specimens and calculated the perfect-match vaccine efficacy using the pepitope model, which quantitated the antigenic drift in the dominant epitope of HA. Phylogenetic analysis of the A(H3N2) HA1 genes classified most strains into genetic clades 1, 3A, 3B, and 3C. The A(H3N2) strains from the 2013 and 2014 seasons showed very low to moderate vaccine efficacy and demonstrated antigenic drift from epitopes C and A to epitope B. Meanwhile, most A(H1N1)pdm09 strains from the 2012-2014 seasons belonged to genetic clades 6A, 6B, and 6C and displayed the dominant epitope mutations at epitopes B and E. Finally, the vaccine efficacy for A(H1N1)pdm09 (79.6-93.4%) was generally higher than that of A(H3N2). These findings further confirmed the accelerating antigenic drift of the circulating influenza A(H3N2) in recent years.
PMID: 26440103 [PubMed - in process] Free full text