The hemagglutinin proteins of clades 1 and 2.3.4.4b H5N1 highly pathogenic avian influenza viruses exhibit comparable attachment patterns to avian and mammalian tissues

The outbreaks of H5N1 highly pathogenic avian influenza (HPAI) virus among US dairy cattle since 2024 have raised concerns of the potential changes in HA receptor binding specificity and tissue tropism. Using insect-cell-expressed recombinant HA proteins derived from clade 1 and circulating clade 2.3.4.4b H5N1 viruses, we showed that the dairy cattle H5 protein retained binding specificity for the avian-like α2,3-linked sialoside 3'SLN over the human-like α2,6-linked sialoside 6'SLNLN, with higher binding affinity to 3'SLN than the other H5 proteins. Clade 1 and 2.3.4.4b H5 proteins showed comparable attachment patterns to the mammary tissues of lactating dairy cattle, which showed high expression of α2,3-linked and α2,6-linked sialyl glycans. All H5 proteins also showed comparable attachment patterns to the lungs of cat, cattle, chicken, ferret, human, and pig. Our results suggest that the recent H5N1 outbreaks in dairy cattle may be related to ecological factors rather than changes in HA receptor binding specificity.

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Publication Details

Journal
Journal of Virology
Published
2025-09-23
DOI
https://doi.org/10.1128/jvi.00976-25
Citations
1
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
1.35
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article

The hemagglutinin proteins of clades 1 and 2.3.4.4b H5N1 highly pathogenic avian influenza viruses exhibit comparable attachment patterns to avian and mammalian tissues

Gilles Foucras, Malik Peiris, Kevin Fung, Christopher J. Brackman et al.
1 citations
Journal of Virology
Influenza Virus Research Studies
1.35
article

The hemagglutinin proteins of clades 1 and 2.3.4.4b H5N1 highly pathogenic avian influenza viruses exhibit comparable attachment patterns to avian and mammalian tissues

Gilles Foucras, Malik Peiris, Kevin Fung, Christopher J. Brackman, Agnès Poujade, Mariette Ducatez, John M. Nicholls, Hui‐Ling Yen, Julia A. Beatty, Nicolas Gaide, Bingkuan Zhu, Hailey Huiyi Feng, Thomas H. C. Sit, Anne C. N. Tse, F. Hill, Shih-Chieh Ti
article en
1 citations

Abstract

The outbreaks of H5N1 highly pathogenic avian influenza (HPAI) virus among US dairy cattle since 2024 have raised concerns of the potential changes in HA receptor binding specificity and tissue tropism. Using insect-cell-expressed recombinant HA proteins derived from clade 1 and circulating clade 2.3.4.4b H5N1 viruses, we showed that the dairy cattle H5 protein retained binding specificity for the avian-like α2,3-linked sialoside 3'SLN over the human-like α2,6-linked sialoside 6'SLNLN, with higher binding affinity to 3'SLN than the other H5 proteins. Clade 1 and 2.3.4.4b H5 proteins showed comparable attachment patterns to the mammary tissues of lactating dairy cattle, which showed high expression of α2,3-linked and α2,6-linked sialyl glycans. All H5 proteins also showed comparable attachment patterns to the lungs of cat, cattle, chicken, ferret, human, and pig. Our results suggest that the recent H5N1 outbreaks in dairy cattle may be related to ecological factors rather than changes in HA receptor binding specificity.

Journal of VirologyVol. 99(10)
City University of Hong Kong (HK), École Nationale Vétérinaire de Toulouse (FR), Chinese University of Hong Kong (HK), Agriculture Fisheries and Conservation Department (CN), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), University of Hong Kong (HK)
Openalex Percentile: Top 15%
Influenza Virus Research Studies
1.35
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