Cell host & microbe, Volume 34, Issue 1, 1 1 2026, Pages 103-115.e9 Molecular basis of 60 years of antigenic evolution of human influenza A(H3N2) virus neuraminidase. Rosu ME, Westgeest KB, de Graaf M, Hauser BM, Tureli S, James S, Sinartio FF, Bestebroer TM, Lexmond P, Pronk MR, van der Vliet S, Skepner E, Spronken MIJ, Mühlemann B, Richard M, Jones TC, Smith DJ, Herfst S, Fouchier RAM
Human influenza A viruses escape antibody-mediated immunity through changes in the hemagglutinin (HA) and neuraminidase (NA) glycoproteins. HA antigenic evolution has been studied extensively, with more recent interest in NA due to its importance in influenza vaccine efficacy. Here, the antigenic properties of the NA of more than 300 A(H3N2) and A(H2N2) viruses isolated since 1957 were quantified with a NA inhibition enzyme-linked lectin assay and visualized using antigenic cartography, with follow-up molecular studies using recombinant viruses. The antigenic evolution of N2 NA was more gradual than that described for H3 HA, and antigenic changes in NA and HA were discordant. Multiple substitutions around the NA active site and tetramer lateral side that alter the charge, volume, or hydropathy of amino acids collectively determined antigenic properties. These data facilitate sequence-based genomic surveillance and inference of antigenic phenotypes from genotypes and offer opportunities to improve influenza vaccine effectiveness through increased focus on NA.
