4.6 Article

H10Nx avian influenza viruses detected in wild birds in China pose potential threat to mammals

Journal

ONE HEALTH
Volume 16, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.onehlt.2023.100515

Keywords

Avian influenza virus; H10 subtype; Wild birds; Phylogeography; Pathogenicity

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In this study, we analyzed the transmission pattern of H10 avian influenza viruses from wild birds to poultry to humans. We identified eight genotypes of H10Nx viruses and found that they replicated efficiently in the respiratory system of mice with low pathogenicity. These wild-bird-origin H10Nx viruses showed asymptomatic shedding in chickens and good adaptation in mice, increasing the risk of transmission to humans and posing a threat to public health.
H10 subtype avian influenza viruses (AIVs) have been isolated from wild and domestic avian species worldwide and have occasionally crossed the species barrier to mammalian hosts. Fatal human cases of H10N8 infections and the recent detection of human H10N3 infections have drawn widespread public attention. In this study, 25 H10Nx viruses were isolated from wild waterfowl in China during a long-term surveillance of AIVs. We con-ducted phylogenetic and phylogeographic studies of the hemagglutinin (HA) genes of global H10 viruses to determine the spatiotemporal patterns of spread and the roles of different hosts in viral transmission. We found the pattern of AIV transmission from wild birds to poultry to humans, and Anatidae have acted as the seeding population in the spread of the virus. Phylogenetic incongruence indicated complex reassortment events and our isolates were divided into eight genotypes (G1-8). We also found that the HA genes of the G8 viruses belonged to the North American lineage, indicating that intercontinental gene flow has occurred. Their receptor-binding specificity showed that the G1/4/5/6/7/8 viruses bind to both human-type & alpha;2,6-linked sialic acid receptors and avian-type & alpha;2,3-linked sialic acid receptors. Mouse studies indicated that the H10Nx isolates replicated efficiently in the respiratory system without preadaptation, but showed low pathogenicity in mice. The H10Nx isolates showed no (G2/4/7) or low pathogenicity (G1/3/5/6/8) in chickens, and the G6 and G8 viruses could be transmitted to chickens through direct contact. The asymptomatic shedding of these wild-bird-origin H10Nx isolates in chickens and their good adaptation in mice should increase the ease of their transmission to humans, and they therefore pose a threat to public health. Our findings demonstrate a further understanding of wild bird-origin H10 viruses and provide information for the continuous surveillance of H10 subtype viruses.

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