His focus has been to better understand how influenza A virus escapes host immunity. The surface proteins of influenza viruses, the hemagglutinin (HA) and neuraminidase (NA), frequently undergo minor amino acid changes, or antigenic drift, resulting in the emergence of new . The A/Fujian . 14 the 1968 pandemic was less extensive due to an antigenic shift only in hemagglutinin gene (from h2n2 to h3n2). The region of antigenic variation that occurs during drift covers the surface of the globular head, especially around the receptor-binding pocket. vaccine virus and circulating seasonal viruses ("antigenic drift"). N2 - Background: The genetic and antigenic characteristics of influenza A viruses (IAV) within and between species change over time due to antigenic shift and drift. In virologic . Antigenic drift was dominantly facilitated at epitopes Sa and Sb of A(H1N1)pdm09, epitopes A, B, D and E of A(H3N2), and the 120 loop and 190 helix of influenza B virus. The findings in mice, using a strain of seasonal influenza virus first isolated in 1934, also suggest that antigenic drift might be slowed by increasing the number of children vaccinated against . All influenza viruses experience some form of antigenic drift, but it is most pronounced in the influenza A virus. These H7N9 variants exhibited a new predomi - nant subclade and had been cocirculating at a low level in eastern and northeastern China. In this study, we induced antigenic drift in an A(H1N1)pdm09 virus in the ferret model. The antigen of H7N9-Re-2 was available from reassortant avian influenza virus trivalent vaccine. Antigenic drift is a kind of genetic variation in viruses, arising from the accumulation of mutations in the virus genes that code for virus-surface proteins that host antibodies recognize. Seasonal epidemics caused by influenza virus are driven by antigenic changes (drift) in viral surface glycoproteins that allow evasion from preexisting humoral immunity. The A/Fujian . Several immune escape mutations and antigenic drift were observed in H7N9 variants. The viral coats, or outer surfaces, of these viruses contain two major antigenic glycoproteins—hemagglutinin (H) and neuraminidase (N)—which differ between influenza A subtypes (e.g., H1N1, H3N2, H5N1). This results in a new strain of virus particles that is not effectively inhibited by the antibodies that prevented infection by previous strains. The subtle mutations accumulated through antigenic drift of . Antigenic drift involves amino acid changes in antigenic regions of influenza vaccine virus and circulating seasonal viruses ("antigenic drift"). Haemagglutination inhibition (HI) tests on antigenic variants selected with 12 different monoclonal antibodies suggested that the antigenic determinants could be subdivided . To date, the 2009 pandemic virus (A(H1N1)pdm09) has not undergone significant antigenic drift, with the result that the vaccine remains well-matched and should provide good protection to A(H1N1)pdm09 circulating viruses. Moderate computed . Since emerging in China in 2013, influenza A (H7N9) viruses have continued to circulate in mainland China, sporadically causing human infection ( 1 - 3 ). •Egg-adapted changes in H3N2 viruses are more complex and likely to have antigenic implications that . Like all living things, influenza makes small errors—mutations—when it copies its genetic code during reproduction. •Egg-adapted changes in H3N2 viruses are more complex and likely to have antigenic implications that . The rate of antigenic drift of swine IAV (swIAV) has generally been believed to be much lower than that of human IAV, mainly due to the short lifespan of pigs and the acute nature of the infection historically seen in pig herds, which limits the impact of pre-existing immunity [3,18,19,20,21,22]. Gething MJ, Bye J, Skehel J, Waterfield M. Cloning and DNA sequence of double-stranded copies of haemagglutinin genes from H2 and H3 strains elucidates antigenic shift and drift in human influenza virus. Once H3N2 became established in humans, the virus began to drift, as is the case with all other human seasonal influenza viruses. Variants of A/PR/8/34 (HON1) influenza virus, having hemagglutinin molecules with probably a single altered antigenic determinant, were isolated by growing the virus in the presence of the monoclonal hybridoma antibody PEG-1. Antigenic variants of A/PR/8/34 [HON1] influenza virus were selected after a single passage of the parent virus in embryonated chicken eggs in the presence of monoclonal antibodies to this virus. These mutations may cause the virus's outer surface to appear different to a host previously infected with the ancestor strain of the virus. All experiments with all available influenza A(H7N9) viruses were conducted in an animal biosafety level 3 laboratory and animal facility under South China Agricultural University (SCAU) (CNAS BL0011) protocols. In 2014-2015 a novel genotype emerged in 3c.2a clade of human H3N2 influenza viruses. Influenza viruses can evolve in a gradual way through mutations in the genes that relate to the viral surface proteins hemagglutinin and neuraminidase (HA and NA in shorthand). Appendix . This is the random accumulation of mutations in the haemagglutinin (HA), and to a lesser extent neuraminidase (NA) genes, recognized by the immune system. Variants of A/PR/8/34 (HON1) influenza virus, having hemagglutinin molecules with probably a single altered antigenic determinant, were isolated by growing the virus in the presence of the monoclonal hybridoma antibody PEG-1. influenza would quickly cease to exist except in chil-dren unless it evolved ways of defeating the immune response. NA antigenic drift has been suggested to occur at lower frequency than HA antigenic drift but can have an impact on influenza spread and antibody recognition of NA [25-27]. Evolution and Antigenic Drift of Influenza A(H7N9) Viruses, China, 2017-2019 . Evolution and Antigenic Drift of Influenza A(H7N9) Viruses, China, 2017-2019 . Antigenic Shift Antigenic shift is a more major change in the influenza virus. The variants were . Several immune escape mutations and antigenic drift were observed in H7N9 variants. 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