Insights into the individual evolutionary origins of Yersinia virulence factor effector proteins

IF 1.8 4区 生物学 Q3 GENETICS & HEREDITY Plasmid Pub Date : 2021-03-01 DOI:10.1016/j.plasmid.2021.102562
Veronica R. Moorman , James I. Cohen
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引用次数: 3

Abstract

Pathogenic Yersinia bacteria, including Y. pseudotubuclosis Y. enterocolitica, and Y. pestis, contain the mosaic plasmid pYV that encodes for, among other things, a number of proteinaceous virulence factors. While the evolutionary histories of many of the biovars and strains of pathogenic Yersinia species are well documented, the origins of many of the individual virulence factors have not been comprehensively examined. Here, the evolutionary origins of the genes coding for a set of Yersinia outer protein (Yop) virulence factors were investigated through phylogenetic reconstruction and subsequence analysis. It was found that many of these genes had only a few sequenced homologs and none of the resolved phylogenies recovered the same relationships as was resolved from chromosomal analyses. Many of the evolutionary relationships differ greatly among genes on the plasmid, and variation is also found across different domains of the same gene, which provides evidence of the mosaic nature of the plasmid as well as multiple genes on the plasmid. This mosaic aspect also relates to patterns of selection, which vary among the studied domains.

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耶尔森氏菌毒力因子效应蛋白的个体进化起源
致病性耶尔森氏菌,包括假管耶尔森氏菌、小肠结肠炎耶尔森氏菌和鼠疫耶尔森氏菌,含有编码多种蛋白毒力因子的镶嵌质粒pYV。虽然许多致病性耶尔森菌物种的生物变种和菌株的进化历史已被很好地记录下来,但许多单个毒力因素的起源尚未得到全面检查。本文通过系统发育重建和子序列分析,研究了一组耶尔森菌外蛋白(Yop)毒力因子编码基因的进化起源。结果发现,其中许多基因只有少数同源序列,没有一个已确定的系统发育恢复了从染色体分析中确定的相同关系。许多进化关系在质粒上的基因之间差异很大,并且在同一基因的不同结构域之间也发现了变异,这为质粒以及质粒上的多个基因的马赛克性质提供了证据。这个镶嵌的方面也涉及到选择的模式,在不同的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plasmid
Plasmid 生物-遗传学
CiteScore
4.70
自引率
3.80%
发文量
21
审稿时长
53 days
期刊介绍: Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.
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