Impact of naturally occurring hemagglutinin substitutions on antigenicity and fitness of influenza A(H5N1) virus

In 2024, a human infection with clade 2.3.4.4b highly pathogenic avian influenza A(H5N1) virus was identified in the United States in an individual with no known exposure. Genetic analysis revealed two hemagglutinin (HA) substitutions, P136S and A156T, which may alter viral antigenicity. Virus isolation was unsuccessful, preventing timely serologic analysis. To overcome this limitation, we generated recombinant viruses by reverse genetics and characterized the effects of the substitutions on antigenicity, receptor binding, and replicative fitness. The A156T substitution introduced a potential N-linked glycosylation site, resulting in altered antigenicity and reduced replication in primary human nasal epithelial cells and ferrets. Importantly, the A(H5N1) candidate vaccine virus (CVV) IDCDC-RG80A, which possesses HA-T156, remained antigenically effective against viruses with and without these substitutions. These findings highlight the importance of sequencing, reverse-genetics approaches, and antigenically similar CVVs such as IDCDC-RG80A, for pandemic preparedness against evolving clade 2.3.4.4b A(H5N1) viruses.

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Publication Details

Journal
npj Viruses
Published
2025-10-01
DOI
https://doi.org/10.1038/s44298-025-00154-5
Citations
3
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
4.06

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article

Impact of naturally occurring hemagglutinin substitutions on antigenicity and fitness of influenza A(H5N1) virus

Chenchen Feng, Sanjay Vashee, Ying Huang, Juan A. De La Cruz et al.
3 citations
npj Viruses
Influenza Virus Research Studies
4.06
article

Impact of naturally occurring hemagglutinin substitutions on antigenicity and fitness of influenza A(H5N1) virus

Chenchen Feng, Sanjay Vashee, Ying Huang, Juan A. De La Cruz, Jaber Hossain, James Stevens, Xudong Lin, Benjamin L. Rambo‐Martin, Yasuko Hatta, Vivien G. Dugan, Nacyra Assad-Garcia, Bin Zhou, P.J. Carney, Gene S. Tan, Juliana DaSilva, C. Todd Davis, Julia C. Frederick, Kristine A. Lacek, Lisa M. Keong, Masato Hatta, Marie K. Kirby, Ginger Atteberry, Jieru Wang, Malania Wilson, Li Wang, Monique Johnson, Michael Currier, Han Di, Rebecca Hart, Sydney Sheffield, Melvyn R Almanzar-Jordan
article en
3 citations

Abstract

In 2024, a human infection with clade 2.3.4.4b highly pathogenic avian influenza A(H5N1) virus was identified in the United States in an individual with no known exposure. Genetic analysis revealed two hemagglutinin (HA) substitutions, P136S and A156T, which may alter viral antigenicity. Virus isolation was unsuccessful, preventing timely serologic analysis. To overcome this limitation, we generated recombinant viruses by reverse genetics and characterized the effects of the substitutions on antigenicity, receptor binding, and replicative fitness. The A156T substitution introduced a potential N-linked glycosylation site, resulting in altered antigenicity and reduced replication in primary human nasal epithelial cells and ferrets. Importantly, the A(H5N1) candidate vaccine virus (CVV) IDCDC-RG80A, which possesses HA-T156, remained antigenically effective against viruses with and without these substitutions. These findings highlight the importance of sequencing, reverse-genetics approaches, and antigenically similar CVVs such as IDCDC-RG80A, for pandemic preparedness against evolving clade 2.3.4.4b A(H5N1) viruses.

npj VirusesVol. 3(1)
Centers for Disease Control and Prevention (US), J. Craig Venter Institute (US), National Center for Immunization and Respiratory Diseases (US), University of California San Diego (US), Office of Readiness and Response (US), Centers for Disease Control and Prevention (UG)
U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, Agency for Toxic Substances and Disease Registry
Openalex Percentile: Top 5%
Influenza Virus Research Studies
4.06
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