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细胞内寄生,嗜肺军团菌和军团菌属进化的驱动力。

Intracellular parasitism, the driving force of evolution of Legionella pneumophila and the genus Legionella.

机构信息

Institut Pasteur, Biologie des Bactéries Intracellulaires and CNRS UMR 3525, 75724, Paris, France.

出版信息

Genes Immun. 2019 May;20(5):394-402. doi: 10.1038/s41435-019-0074-z. Epub 2019 May 4.

Abstract

Legionella pneumophila is an intracellular pathogen that causes a severe pneumonia called Legionnaires' disease that is often fatal when not promptly diagnosed and treated. However, L. pneumophila is mainly an environmental pathogen of protozoa. This bacterium parasitizes free-living amoeba and other aquatic protozoa with which it co-evolved over an evolutionary long time. Due to the close relationship between hosts and pathogens, their co-evolution leads to molecular interactions such as the exchange of genetic material through horizontal gene transfer (HGT). Those genes that confer an advantage to the bacteria were fixed in their genomes and help these pathogens to subvert host functions to their advantage. Genome sequencing of L. pneumophila and recently of the entire genus Legionella that comprises over 60 species revealed that Legionellae have co-opted genes and thus cellular functions from their eukaryotic hosts to a surprisingly high extent never observed before for an prokaryotic organism. Acquisition and loss of these eukaryotic-like genes and eukaryotic domains is an ongoing process underlining the highly dynamic nature of the Legionella genomes. Although the large amount and diversity of HGT that occurred between Legionella and their protozoan hosts seems to be unique in the prokaryotic world, the analyses of more and more genomes from environmental organisms and symbionts of amoeba revealed that such genetic exchanges occur among all amoeba-associated bacteria and also among the different microorganisms that infect amoeba such as viruses. This dynamic reshuffling and gene-acquisition has led to the emergence of major human pathogens such as Legionella and may lead to the emergence of new human pathogens from the environment.

摘要

嗜肺军团菌是一种细胞内病原体,可引起严重肺炎,称为军团病,如果不及时诊断和治疗,通常是致命的。然而,嗜肺军团菌主要是原生动物的环境病原体。这种细菌寄生在自由生活的变形虫和其他水生原生动物中,与它们共同进化了很长时间。由于宿主和病原体之间的密切关系,它们的共同进化导致了分子相互作用,例如通过水平基因转移(HGT)交换遗传物质。那些赋予细菌优势的基因在其基因组中固定下来,帮助这些病原体颠覆宿主功能以获得优势。嗜肺军团菌的基因组测序以及最近对整个军团菌属(包含 60 多种物种)的基因组测序表明,军团菌从其真核宿主中获得了基因,并因此获得了细胞功能,这在以前从未观察到过原核生物。这些真核样基因和真核结构域的获得和丧失是一个持续的过程,强调了军团菌基因组高度动态的性质。尽管军团菌与其原生动物宿主之间发生的大量和多样化的 HGT 似乎在原核世界中是独一无二的,但对越来越多的来自环境生物和变形虫共生体的基因组进行分析表明,这种遗传交换发生在所有与变形虫相关的细菌之间,也发生在感染变形虫的不同微生物(如病毒)之间。这种动态重排和基因获取导致了主要人类病原体的出现,如军团菌,并且可能导致来自环境的新的人类病原体的出现。

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