非志贺氧致肠聚集性大肠杆菌O104:H4爆发株毒力质粒的遗传和表型分析。

IF 2.6 4区 生物学 Q3 MICROBIOLOGY
Rachel Whelan, Martyna Cyganek, Charlotte L Oxley, Benjamin Dickins, Jonathan C Thomas, Gareth McVicker
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引用次数: 0

摘要

肠聚集性大肠杆菌O104:H4最为人所知的是,它在2011年引发了一次全球疫情,原因是它获得了一种志贺样毒素,同时具有传统的肠聚集性毒力特征;然而,尽管对2011年爆发的菌株进行了充分的研究,但对O104:H4的毒力质粒进行的实验分析却少得多。在本文中,我们分析了pAA毒力质粒对非志贺氧原性O104:H4菌株(1070/13)的遗传和表型贡献,尽管如此,该菌株仍与2013年英国大规模暴发有关。我们发现pAA1070在88%的质粒序列上与2011年爆发菌株的pTY2有99.95%的相同,每条染色体的拷贝数约为2-3个质粒分子。我们证明pAA1070携带功能性CcdAB质粒成瘾系统,在测试条件下仅对其稳定性产生轻微影响。质粒编码的其他毒素-抗毒素系统似乎都不起作用,尽管我们注意到质粒在体外具有惊人的高稳定性。我们证明了pAA1070对肠细胞粘附的预期贡献,但发现它对生物膜的形成没有贡献。在评估pAA1070对运动性的影响时,我们发现O104:H4染色体的一个区域可以被切除,通过截断fliR基因来消除运动性。最终,这项工作证明了移动遗传元件对肠聚集性大肠杆菌作为其自身的致病变种的重要性,并强调了为了了解毒力表型,通过实验表征真正的爆发菌株而不是实验室菌株的复杂性和必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic and phenotypic analysis of the virulence plasmid of a non-Shigatoxigenic enteroaggregative Escherichia coli O104:H4 outbreak strain.

Enteroaggregative Escherichia coli O104:H4 is best known for causing a worldwide outbreak in 2011 due to the acquisition of a Shiga-like toxin alongside traditional enteroaggregative virulence traits; however, whilst the 2011 outbreak strain has been well studied, the virulence plasmid of O104:H4 has been subjected to far less experimental analysis. In this paper, we analyse the genetic and phenotypic contribution of the pAA virulence plasmid to a non-Shigatoxigenic O104:H4 strain (1070/13) that was nonetheless implicated in a substantial UK outbreak in 2013. We find that pAA1070 is 99.95% identical across 88% of the plasmid sequence to pTY2 from the 2011 outbreak strain and has a copy number of ~2-3 plasmid molecules per chromosome. We demonstrate that pAA1070 carries a functional CcdAB plasmid addiction system that only marginally impacts its stability under the conditions tested. None of the other toxin-antitoxin systems encoded by the plasmid appear to be functional, though we note a surprisingly high stability of the plasmid in vitro regardless. We demonstrate the expected contribution of pAA1070 to intestinal cell adhesion but find that it does not contribute to biofilm formation. When assessing the impact of pAA1070 on motility, we discovered a region of the O104:H4 chromosome that can be excised, abolishing motility via truncation of the fliR gene. Ultimately, this work demonstrates the importance of mobile genetic elements to enteroaggregative E. coli as a pathovar in its own right and highlights the complexity but necessity of experimentally characterizing genuine outbreak strains rather than laboratory strains in order to understand virulence phenotypes.

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来源期刊
Microbiology-Sgm
Microbiology-Sgm 生物-微生物学
CiteScore
4.60
自引率
7.10%
发文量
132
审稿时长
3.0 months
期刊介绍: We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms. Topics include but are not limited to: Antimicrobials and antimicrobial resistance Bacteriology and parasitology Biochemistry and biophysics Biofilms and biological systems Biotechnology and bioremediation Cell biology and signalling Chemical biology Cross-disciplinary work Ecology and environmental microbiology Food microbiology Genetics Host–microbe interactions Microbial methods and techniques Microscopy and imaging Omics, including genomics, proteomics and metabolomics Physiology and metabolism Systems biology and synthetic biology The microbiome.
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