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中国两株新型 2.3.2.1 分支 H5N2 亚型禽流感病毒的系统进化和表型特征。

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

机构信息

Animal Infectious Diseases Laboratory, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China.

Animal Infectious Diseases Laboratory, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China; Yangzhou Customs, Yangzhou, Jiangsu 225009, China.

出版信息

Infect Genet Evol. 2022 Mar;98:105205. doi: 10.1016/j.meegid.2022.105205. Epub 2022 Jan 5.

Abstract

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 10EID 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.

摘要

H5 亚型高致病性禽流感(HPAI)病毒和 H9N2 低致病性禽流感(LPAI)病毒的广泛共同循环不可避免地促进了这两种亚型在田间的基因重组。而且,不断检测到携带部分甚至整套 H9N2 内部基因的新型重配 H5NX 病毒,例如 2.3.4.4 分支的 H5N2 或 H5N6 重配体。在这里,我们报告了 2018 年在活禽市场常规监测中从鸡中分离到的两种新型 H5N2 亚型 HPAI 分离株 HF9 和 QY5。系统进化分析表明,这两种 H5N2 株均具有来自 H5N1 病毒 2.3.2.1e 分支的 HA 基因,但其他七个基因片段均来自 H9N2 亚型病毒的地方性 S 基因型。进一步分析表明,HF9 和 QY5 仅在六个位点上存在差异,包括 PB2 中的 K353R、A588T 和 T661I,PB1 中的 I682V 和 L704S 以及 PA 中的 G631S。鸡回归实验证实,HF9 和 QY5 均可通过接触传播对所有测试鸡造成致死性感染。此外,这两种分离株无需适应即可立即在小鼠肺部复制。然而,这两种变异体在小鼠模型中的死亡率存在明显差异,HF9 的死亡率为 100%,QY5 的死亡率为 20%,感染剂量为每只小鼠 10EID。我们假设表型差异可能归因于这两种分离株聚合酶基因中的氨基酸替换,这是我们正在进行的进一步研究的主题。

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