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Recent H3N2 Influenza Virus Clinical Isolates Rapidly Acquire Hemagglutinin or Neuraminidase Mutations When Propagated for Antigenic Analyses
Author(s) -
Benjamin S. Chambers,
Yang Li,
Richard L. Hodinka,
Scott E. Hensley
Publication year - 2014
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01077-14
Subject(s) - biology , virology , neuraminidase , avidity , hemagglutinin (influenza) , virus , antigenic drift , h5n1 genetic structure , serology , antigenic shift , influenza a virus , microbiology and biotechnology , orthomyxoviridae , antigen , epitope , antibody , immunology , covid-19 , infectious disease (medical specialty) , pathology , medicine , disease
Prior to serological testing, influenza viruses are typically propagated in eggs or cell culture. Recent human H3N2 strains bind to cells with low avidity. Here, we isolated nine primary H3N2 viral isolates from respiratory secretions of children. Upon propagation in vitro, five of these isolates acquired hemagglutinin or neuraminidase mutations that increased virus binding to cell surfaces. These mutations can potentially confound serological assays commonly used to identify antigenically novel influenza viruses.

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