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利用小鼠模型评估从蒙古野鸭蛋粪便中分离出的新型高致病性禽流感(H5N6)病毒的潜在致病性。

Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model.

机构信息

Zoonosis Research Center, Department of Infection Biology, School of Medicine, Wonkwang University, Iksan, Korea.

State Central Veterinary Laboratory, Zaisan, Ulaanbaatar, Mongolia.

出版信息

Emerg Microbes Infect. 2022 Dec;11(1):1425-1434. doi: 10.1080/22221751.2022.2069515.

Abstract

Several novel highly pathogenic avian influenza (HPAIVs) A(H5N6) viruses were reported in Mongolia in 2020, some of which included host-specific markers associated with mammalian infection. However, their pathogenicity has not yet been investigated. Here, we isolated and evaluate two novel genotypes of A(H5N6) subtype in Mongolia during 2018-2019 (A/wildDuck/MN/H5N6/2018-19). Their evolution pattern and molecular characteristics were evaluated using gene sequencing and their pathogenicity was determined using a mouse model. We also compared their antigenicity with previous H5 Clade 2.3.4.4 human isolates by cross-hemagglutination inhibition (HI). Our data suggests that A/wildDuck/MN/H5N6/2018-19 belongs to clade 2.3.4.4h, and maintains several residues associated with mammal adaptation. In addition, our evaluations revealed that their isolates are less virulent in mice than the previously identified H5 human isolates. However, their antigenicity is distinct from other HPAIVs H5 clade 2.3.4.4, thus supporting their continued evaluation as potential infection risks and the preparation of novel candidate vaccines for their neutralization.

摘要

2020 年,蒙古报告了几株新型高致病性禽流感(HPAIV)A(H5N6)病毒,其中一些病毒包含与哺乳动物感染相关的宿主特异性标记物。然而,它们的致病性尚未得到研究。在这里,我们在 2018-2019 年期间从蒙古分离和评估了两种新型的 A(H5N6)亚型的基因型(A/野禽/MN/H5N6/2018-19)。我们通过基因测序评估了它们的进化模式和分子特征,并使用小鼠模型确定了它们的致病性。我们还通过血凝抑制(HI)交叉试验比较了它们与以前的 H5 分支 2.3.4.4 人类分离株的抗原性。我们的数据表明,A/野禽/MN/H5N6/2018-19 属于 2.3.4.4h 分支,并且保持了与哺乳动物适应相关的几个残基。此外,我们的评估结果表明,与之前鉴定的 H5 人类分离株相比,这些分离株在小鼠中的毒力较低。然而,它们的抗原性与其他 HPAIVs H5 分支 2.3.4.4 不同,因此支持继续评估它们作为潜在感染风险的候选,并为它们的中和作用制备新型候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7616/9154755/7d13445e68d2/TEMI_A_2069515_F0001_OC.jpg

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