Positive Selection on Hemagglutinin and Neuraminidase Genes of H1N1 Influenza Viruses

Hdl Handle:
http://hdl.handle.net/10147/129409
Title:
Positive Selection on Hemagglutinin and Neuraminidase Genes of H1N1 Influenza Viruses
Authors:
Li, Wenfu; Shi, Weifeng; Qiao, Huijie; Ho, Simon Y.W.; Luo, Arong; Zhang, Yanzhou; Zhu, Chaodong
Citation:
Virology Journal. 2011 Apr 21;8(1):183
Issue Date:
21-Apr-2011
URI:
http://hdl.handle.net/10147/129409
Abstract:
Abstract Background Since its emergence in March 2009, the pandemic 2009 H1N1 influenza A virus has posed a serious threat to public health. To trace the evolutionary path of these new pathogens, we performed a selection-pressure analysis of a large number of hemagglutinin (HA) and neuraminidase (NA) gene sequences of H1N1 influenza viruses from different hosts. Results Phylogenetic analysis revealed that both HA and NA genes have evolved into five distinct clusters, with further analyses indicating that the pandemic 2009 strains have experienced the strongest positive selection. We also found evidence of strong selection acting on the seasonal human H1N1 isolates. However, swine viruses from North America and Eurasia were under weak positive selection, while there was no significant evidence of positive selection acting on the avian isolates. A site-by-site analysis revealed that the positively selected sites were located in both of the cleaved products of HA (HA1 and HA2), as well as NA. In addition, the pandemic 2009 strains were subject to differential selection pressures compared to seasonal human, North American swine and Eurasian swine H1N1 viruses. Conclusions Most of these positively and/or differentially selected sites were situated in the B-cell and/or T-cell antigenic regions, suggesting that selection at these sites might be responsible for the antigenic variation of the viruses. Moreover, some sites were also associated with glycosylation and receptor-binding ability. Thus, selection at these positions might have helped the pandemic 2009 H1N1 viruses to adapt to the new hosts after they were introduced from pigs to humans. Positive selection on position 274 of NA protein, associated with drug resistance, might account for the prevalence of drug-resistant variants of seasonal human H1N1 influenza viruses, but there was no evidence that positive selection was responsible for the spread of the drug resistance of the pandemic H1N1 strains.
Item Type:
Journal Article

Full metadata record

DC FieldValue Language
dc.contributor.authorLi, Wenfu-
dc.contributor.authorShi, Weifeng-
dc.contributor.authorQiao, Huijie-
dc.contributor.authorHo, Simon Y.W.-
dc.contributor.authorLuo, Arong-
dc.contributor.authorZhang, Yanzhou-
dc.contributor.authorZhu, Chaodong-
dc.date.accessioned2011-05-11T10:39:58Z-
dc.date.available2011-05-11T10:39:58Z-
dc.date.issued2011-04-21-
dc.identifierhttp://dx.doi.org/10.1186/1743-422X-8-183-
dc.identifier.citationVirology Journal. 2011 Apr 21;8(1):183-
dc.identifier.urihttp://hdl.handle.net/10147/129409-
dc.description.abstractAbstract Background Since its emergence in March 2009, the pandemic 2009 H1N1 influenza A virus has posed a serious threat to public health. To trace the evolutionary path of these new pathogens, we performed a selection-pressure analysis of a large number of hemagglutinin (HA) and neuraminidase (NA) gene sequences of H1N1 influenza viruses from different hosts. Results Phylogenetic analysis revealed that both HA and NA genes have evolved into five distinct clusters, with further analyses indicating that the pandemic 2009 strains have experienced the strongest positive selection. We also found evidence of strong selection acting on the seasonal human H1N1 isolates. However, swine viruses from North America and Eurasia were under weak positive selection, while there was no significant evidence of positive selection acting on the avian isolates. A site-by-site analysis revealed that the positively selected sites were located in both of the cleaved products of HA (HA1 and HA2), as well as NA. In addition, the pandemic 2009 strains were subject to differential selection pressures compared to seasonal human, North American swine and Eurasian swine H1N1 viruses. Conclusions Most of these positively and/or differentially selected sites were situated in the B-cell and/or T-cell antigenic regions, suggesting that selection at these sites might be responsible for the antigenic variation of the viruses. Moreover, some sites were also associated with glycosylation and receptor-binding ability. Thus, selection at these positions might have helped the pandemic 2009 H1N1 viruses to adapt to the new hosts after they were introduced from pigs to humans. Positive selection on position 274 of NA protein, associated with drug resistance, might account for the prevalence of drug-resistant variants of seasonal human H1N1 influenza viruses, but there was no evidence that positive selection was responsible for the spread of the drug resistance of the pandemic H1N1 strains.-
dc.titlePositive Selection on Hemagglutinin and Neuraminidase Genes of H1N1 Influenza Viruses-
dc.typeJournal Article-
dc.language.rfc3066en-
dc.rights.holderLi et al.; licensee BioMed Central Ltd.-
dc.description.statusPeer Reviewed-
dc.date.updated2011-05-10T16:04:28Z-
All Items in Lenus, The Irish Health Repository are protected by copyright, with all rights reserved, unless otherwise indicated.