| Literature DB >> 34542812 |
Kaituo Liu1, Pingyun Ding1, Yuru Pei1, Ruyi Gao1,2,3, Wenwen Han1, Huafen Zheng1, Zhuxing Ji1, Miao Cai1, Jinyuan Gu1, Xiuli Li1, Min Gu1,2,3, Jiao Hu1,2,3, Xiaowen Liu1,2,3, Shunlin Hu1,2,3, Pinghu Zhang4, Xiaobo Wang1, Xiaoquan Wang5,6,7, Xiufan Liu8,9,10.
Abstract
Decades have passed since the first discovery of H10-subtype avian influenza virus (AIV) in chickens in 1949, and it has been detected in many species including mammals such as minks, pigs, seals and humans. Cases of human infections with H10N8 viruses identified in China in 2013 have raised widespread attention. Two novel reassortant H10N3 viruses were isolated from chickens in December 2019 in eastern China during routine surveillance for AIVs. The internal genes of these viruses were derived from genotype S (G57) H9N2 and were consistent with H5N6, H7N9 and H10N8, which cause fatal infections in humans. Their viral pathogenicity and transmissibility were further studied in different animal models. The two H10N3 isolates had low pathogenicity in chickens and were transmitted between chickens via direct contact. These viruses were highly pathogenic in mice and could be transmitted between guinea pigs via direct contact and respiratory droplets. More importantly, these viruses can bind to both human-type SAα-2,6-Gal receptors and avian-type SAα-2,3-Gal receptors. Asymptomatic shedding in chickens and good adaptability to mammals of these H10N3 isolates would make it easier to transmit to humans and pose a threat to public health.Entities:
Keywords: H10N3; H9N2; pathogenicity; receptor binding; respiratory droplet transmissibility
Mesh:
Year: 2021 PMID: 34542812 DOI: 10.1007/s11427-020-1981-5
Source DB: PubMed Journal: Sci China Life Sci ISSN: 1674-7305 Impact factor: 6.038