Large scale genome analysis shows that the epitopes for broadly cross-reactive antibodies are predominant in the pandemic 2009 influenza virus A H1N1 strain
- PMID: 24257096
- PMCID: PMC3856415
- DOI: 10.3390/v5112796
Large scale genome analysis shows that the epitopes for broadly cross-reactive antibodies are predominant in the pandemic 2009 influenza virus A H1N1 strain
Abstract
The past pandemic strain H1N1 (A (H1N1)pdm09) has now become a common component of current seasonal influenza viruses. It has changed the pre-existing immunity of the human population to succeeding infections. In the present study, a total of 14,210 distinct sequences downloaded from National Center for Biotechnology Information (NCBI) database were used for the analysis. The epitope compositions in A (H1N1)pdm09, classic seasonal strains, swine strains as well as highly virulent avian strain H5N1, identified with the aid of the Immune Epitope DataBase (IEDB), were compared at genomic level. The result showed that A (H1N1) pdm09 contains the 90% of B-cell epitopes for broadly cross-reactive antibodies (EBCA), which is in consonance with the recent reports on the experimental identification of new epitopes or antibodies for this virus and the binding tests with influenza virus protein HA of different subtypes. Our analysis supports that high proportional EBCA depends on the epitope pattern of A (H1N1)pdm09 virus. This study may be helpful for better understanding of A (H1N1)pdm09 and the production of new influenza vaccines.
Similar articles
-
Molecular basis for broad neuraminidase immunity: conserved epitopes in seasonal and pandemic H1N1 as well as H5N1 influenza viruses.J Virol. 2013 Aug;87(16):9290-300. doi: 10.1128/JVI.01203-13. Epub 2013 Jun 19. J Virol. 2013. PMID: 23785204 Free PMC article.
-
Cross-reactive immunity against influenza viruses in children and adults following 2009 pandemic H1N1 infection.Antiviral Res. 2015 Feb;114:106-12. doi: 10.1016/j.antiviral.2014.12.008. Epub 2014 Dec 13. Antiviral Res. 2015. PMID: 25513756
-
Pre-existing immunity with high neutralizing activity to 2009 pandemic H1N1 influenza virus in Shanghai population.PLoS One. 2013;8(3):e58810. doi: 10.1371/journal.pone.0058810. Epub 2013 Mar 19. PLoS One. 2013. PMID: 23527030 Free PMC article.
-
One step closer to universal influenza epitopes.Expert Rev Anti Infect Ther. 2009 Aug;7(6):687-90. doi: 10.1586/eri.09.48. Expert Rev Anti Infect Ther. 2009. PMID: 19681695 Review.
-
Immunity to seasonal and pandemic influenza A viruses.Microbes Infect. 2011 May;13(5):489-501. doi: 10.1016/j.micinf.2011.01.007. Epub 2011 Feb 2. Microbes Infect. 2011. PMID: 21295153 Free PMC article. Review.
Cited by
-
Heterologous Humoral Response against H5N1, H7N3, and H9N2 Avian Influenza Viruses after Seasonal Vaccination in a European Elderly Population.Vaccines (Basel). 2017 Jul 17;5(3):17. doi: 10.3390/vaccines5030017. Vaccines (Basel). 2017. PMID: 28714923 Free PMC article.
References
-
- Centers for Disease Control and Prevention. National and Regional Level Outpatient Illness and Viral Surveillance. [(accessed on 10 November 2012)]. Available online: http://gis.cdc.gov/grasp/fluview/fluportaldashboard.html.
-
- Wrammert J., Koutsonanos D., Li G.M., Edupuganti S., Sui J., Morrissey M., McCausland M., Skountzou I., Hornig M., Lipkin W.I., et al. Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection. J. Exp. Med. 2011;208:181–193. doi: 10.1084/jem.20101352. - DOI - PMC - PubMed
-
- Li G.M., Chiu C., Wrammert J., McCausland M., Andrews S.F., Zheng N.Y., Lee J.H., Huang M., Qu X., Edupuganti S., et al. Pandemic H1N1 influenza vaccine induces a recall response in humans that favors broadly cross-reactive memory B cells. Proc. Natl. Acad. Sci. USA. 2012;109:9047–9052. doi: 10.1073/pnas.1118979109. - DOI - PMC - PubMed
-
- Chen Y., Qin K., Wu W.L., Li G., Zhang J., Du H., Ng M.H., Shih J.W., Peiris J.S., Guan Y., et al. Broad cross-protection against H5N1 avian influenza virus infection by means of monoclonal antibodies that map to conserved viral epitopes. J. Infect. Dis. 2009;199:49–58. doi: 10.1086/594374. - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous