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大肠杆菌 ST131 的进化之谜。

The evolutionary puzzle of Escherichia coli ST131.

机构信息

Department of Pathology and Laboratory Medicine, Cummings School of Medicine, 3330 Hospital Dr NW, Calgary, Alberta T2N 4N1, Canada; Department of Medical Microbiology, University of Pretoria, Pretoria, Gauteng, South Africa; Division of Microbiology, Alberta Precision Laboratories, 3535 Research Rd NW, Calgary, Alberta T2L 2K8, Canada.

Department of Microbiology, Immunology & Infectious Diseases, Cummings School of Medicine, 3330 Hospital Dr NW, Calgary, Alberta T2N 4N1, Canada.

出版信息

Infect Genet Evol. 2020 Jul;81:104265. doi: 10.1016/j.meegid.2020.104265. Epub 2020 Feb 26.

Abstract

The abrupt expansion of Escherichia coli sequence type (ST) 131 is unmatched among Gram negative bacteria. In many ways, ST131 can be considered a real-world model for the complexities involved in the evolution of a multidrug resistant pathogen. While much progress has been made on our insights into the organism's population structure, pathogenicity and drug resistance profile, significant gaps in our knowledge remain. Whole genome studies have shed light on key mutations and genes that have been selected against the background of antibiotics, but in most cases such events are inferred and not supported by experimental data. Notable examples include the unknown fitness contribution made by specific plasmids, genomic islands and compensatory mutations. Furthermore, questions remain like why this organism in particular achieved such considerable success in such a short time span, compared to other more pathogenic and resistant clones. Herein, we document what is known regarding the genetics of this organism since its first description in 2008, but also highlight where work remains to be done for a truly comprehensive understanding of the biology of ST131, in order to account for its dramatic rise to prominence.

摘要

大肠杆菌序列型(ST)131 的突然扩张在革兰氏阴性菌中是无与伦比的。在许多方面,ST131 可以被视为一个多药耐药病原体进化过程中所涉及的复杂性的真实世界模型。尽管我们对该生物的种群结构、致病性和耐药性特征有了很多了解,但仍存在许多知识空白。全基因组研究揭示了在抗生素背景下被选择的关键突变和基因,但在大多数情况下,这些事件是推断出来的,而不是由实验数据支持的。值得注意的例子包括特定质粒、基因组岛和补偿突变的未知适应度贡献。此外,还有一些问题仍然存在,例如为什么与其他更具致病性和耐药性的克隆相比,这种生物在如此短的时间内取得了如此大的成功。本文记录了自 2008 年首次描述以来该生物的遗传学研究进展,但也强调了为了全面了解 ST131 的生物学特性,仍有工作需要做,以解释其为何如此迅速地引人注目。

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