Phylogenetic and phenotypic characterization of two novel clade 2.3.2.1 H5N2 subtype avian influenza viruses from chickens in China

文献类型： 外文期刊

第一作者： Ge, Zhichuang

作者： Ge, Zhichuang;Xu, Lijun;Hu, Xiaomiao;Zhu, Shanshan;Zhao, Ying;Li, Yang;Liu, Kaituo;Gao, Ruyi;Wang, Xiaoquan;Hu, Jiao;Liu, Xiaowen;Hu, Shunlin;Peng, Daxin;Gu, Min;Liu, Xiufan;Xu, Lijun;Hu, Xiaomiao;Gao, Ruyi;Wang, Xiaoquan;Hu, Jiao;Liu, Xiaowen;Hu, Shunlin;Peng, Daxin;Gu, Min;Liu, Xiufan

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关键词： Avian influenza; Clade 2.3.2.1; Novel H5N2; Phylogenetic analysis; Pathogenicity

期刊名称：INFECTION GENETICS AND EVOLUTION （ 影响因子：4.393； 五年影响因子：3.656 ）

ISSN： 1567-1348

年卷期： 2022 年 98 卷

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收录情况： SCI

摘要： The extended co-circulation of H5 subtype highly pathogenic avian influenza (HPAI) viruses and H9N2 low pathogenic avian influenza (LPAI) viruses has inevitably facilitated gene reassortment between the two subtypes in fields. And, novel reassortant H5NX viruses harboring partial or even whole sets of H9N2 internal genes have continuously been detected, such as clade 2.3.4.4 H5N2 or H5N6 reassortants. Here, we report two novel H5N2 subtype HPAI isolates of HF9 and QY5 from chickens in live poultry markets during routine surveillance in 2018. Phylogenetic analysis showed that those two H5N2 strains both possessed the HA genes from clade 2.3.2.1e of H5N1 viruses but all the other seven gene segments consistently from the endemic S genotype of H9N2 subtype viruses. Further analysis revealed that HF9 and QY5 differed only in six sites including K353R, A588T and T661I in PB2, I682V and L704S in PB1 plus G631S in PA at the amino acid level. A chicken regression experiment confirmed that both HF9 and QY5 were lethal infection to all tested chickens via contact transmission. Moreover, those two isolates could immediately replicate in mice lungs without adaptation. However, mortality rate of those two variants were distinct in mice model, HF9 with 100% but QY5 with just 20% at the infection dosage of 106.0EID50 per mouse. We suppose that the phenotypic difference may probably be attributed to the amino acid substitutions in the polymerase genes between the two isolates that constitute of a subject of further ongoing research

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