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新兴小核糖核酸病毒的遗传多样性与进化。

Genetic diversity and evolution of the emerging picornavirus .

机构信息

Embrapa Swine and Poultry, Concórdia, Santa Catarina, Brazil.

Department of Veterinary and Biomedical Sciences, Animal Disease Research and Diagnostic Laboratory, South Dakota State University, Brookings, SD 57007, USA.

出版信息

J Gen Virol. 2020 Feb;101(2):175-187. doi: 10.1099/jgv.0.001360. Epub 2019 Dec 20.

Abstract

(SVA) is an emerging picornavirus that causes vesicular disease (VD) in swine. The virus has been circulating in swine in the United Stated (USA) since at least 1988, however, since 2014 a marked increase in the number of SVA outbreaks has been observed in swine worldwide. The factors that led to the emergence of SVA remain unknown. Evolutionary changes that accumulated in the SVA genome over the years may have contributed to the recent increase in disease incidence. Here we compared full-genome sequences of historical SVA strains (identified before 2010) from the USA and global contemporary SVA strains (identified after 2011). The results from the genetic analysis revealed 6.32 % genetic divergence between historical and contemporary SVA isolates. Selection pressure analysis revealed that the SVA polyprotein is undergoing selection, with four amino acid (aa) residues located in the VP1 (aa 735), 2A (aa 941), 3C (aa 1547) and 3D (aa 1850) coding regions being under positive/diversifying selection. Several aa substitutions were observed in the structural proteins (VP1, VP2 and VP3) of contemporary SVA isolates when compared to historical SVA strains. Some of these aa substitutions led to changes in the surface electrostatic potential of the structural proteins. This work provides important insights into the molecular evolution and epidemiology of SVA.

摘要

(SVA) 是一种新兴的小核糖核酸病毒,可引起猪的水疱病 (VD)。自 1988 年以来,该病毒一直在美国的猪群中传播,但自 2014 年以来,全球范围内 SVA 的爆发数量明显增加。导致 SVA 出现的因素仍不清楚。SVA 基因组中多年来积累的进化变化可能导致了最近疾病发病率的增加。在这里,我们比较了来自美国的历史 SVA 株(2010 年前鉴定)和全球当代 SVA 株(2011 年后鉴定)的全基因组序列。遗传分析的结果显示,历史和当代 SVA 分离株之间存在 6.32%的遗传差异。选择压力分析表明,SVA 多蛋白正在经历选择,VP1(aa735)、2A(aa941)、3C(aa1547)和 3D(aa1850)编码区的四个氨基酸 (aa) 残基受到正/多样化选择的影响。与历史 SVA 株相比,当代 SVA 分离株的结构蛋白(VP1、VP2 和 VP3)中观察到一些 aa 取代。这些 aa 取代中的一些导致结构蛋白表面静电势发生变化。这项工作为 SVA 的分子进化和流行病学提供了重要的见解。

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