Predicting the antigenic evolution of seasonal influenza viruses using phylogenetic convergence

The antigenic evolution of human seasonal influenza viruses is primarily driven by single amino acid substitutions immediately adjacent to the receptor binding site in the hemagglutinin (HA) protein. The ability to predict these substitutions would allow vaccine strains to be selected with an understanding of likely future antigenic variation. Here, we estimate the effect of HA substitutions on viral fitness using measurements of convergent evolution in a large phylogeny. We show that the substitutions which have historically caused major antigenic changes in H3N2 influenza viruses were nearly always one of few substitutions near the HA receptor binding site estimated to be under positive selection in sequences collected before the antigenic transition, based on convergent acquisition of the substitution in multiple independent lineages. Furthermore, this signal predates the establishment of the major clade containing the antigenic substitution by more than one year, so is highly informative for prospective prediction.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-04-10
DOI
https://doi.org/10.64898/2026.04.10.717627
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Predicting the antigenic evolution of seasonal influenza viruses using phylogenetic convergence

David J. Pattinson, Samuel A. Turner, Derek J. Smith, Ron A. M. Fouchier
bioRxiv (Cold Spring Harbor Laboratory)
Influenza Virus Research Studies
article

Predicting the antigenic evolution of seasonal influenza viruses using phylogenetic convergence

David J. Pattinson, Samuel A. Turner, Derek J. Smith, Ron A. M. Fouchier
article en

Abstract

The antigenic evolution of human seasonal influenza viruses is primarily driven by single amino acid substitutions immediately adjacent to the receptor binding site in the hemagglutinin (HA) protein. The ability to predict these substitutions would allow vaccine strains to be selected with an understanding of likely future antigenic variation. Here, we estimate the effect of HA substitutions on viral fitness using measurements of convergent evolution in a large phylogeny. We show that the substitutions which have historically caused major antigenic changes in H3N2 influenza viruses were nearly always one of few substitutions near the HA receptor binding site estimated to be under positive selection in sequences collected before the antigenic transition, based on convergent acquisition of the substitution in multiple independent lineages. Furthermore, this signal predates the establishment of the major clade containing the antigenic substitution by more than one year, so is highly informative for prospective prediction.

bioRxiv (Cold Spring Harbor Laboratory)
University of Wisconsin–Madison (US), University of Cambridge (GB), Erasmus MC (NL), Erasmus University Rotterdam (NL)
Openalex Percentile: Top 24%
Influenza Virus Research Studies
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