David Sophia, Rusniok Christophe, Mentasti Massimo, Gomez-Valero Laura, Harris Simon R, Lechat Pierre, Lees John, Ginevra Christophe, Glaser Philippe, Ma Laurence, Bouchier Christiane, Underwood Anthony, Jarraud Sophie, Harrison Timothy G, Parkhill Julian, Buchrieser Carmen
Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA Cambridge, United Kingdom.
Public Health England, NW9 5HT London, United Kingdom.
Genome Res. 2016 Nov;26(11):1555-1564. doi: 10.1101/gr.209536.116. Epub 2016 Sep 23.
Legionella pneumophila is an environmental bacterium and the leading cause of Legionnaires' disease. Just five sequence types (ST), from more than 2000 currently described, cause nearly half of disease cases in northwest Europe. Here, we report the sequence and analyses of 364 L. pneumophila genomes, including 337 from the five disease-associated STs and 27 representative of the species diversity. Phylogenetic analyses revealed that the five STs have independent origins within a highly diverse species. The number of de novo mutations is extremely low with maximum pairwise single-nucleotide polymorphisms (SNPs) ranging from 19 (ST47) to 127 (ST1), which suggests emergences within the last century. Isolates sampled geographically far apart differ by only a few SNPs, demonstrating rapid dissemination. These five STs have been recombining recently, leading to a shared pool of allelic variants potentially contributing to their increased disease propensity. The oldest clone, ST1, has spread globally; between 1940 and 2000, four new clones have emerged in Europe, which show long-distance, rapid dispersal. That a large proportion of clinical cases is caused by recently emerged and internationally dispersed clones, linked by convergent evolution, is surprising for an environmental bacterium traditionally considered to be an opportunistic pathogen. To simultaneously explain recent emergence, rapid spread and increased disease association, we hypothesize that these STs have adapted to new man-made environmental niches, which may be linked by human infection and transmission.
嗜肺军团菌是一种环境细菌,也是军团病的主要病因。在目前已描述的2000多种序列类型中,仅有5种序列类型导致了西北欧近一半的病例。在此,我们报告了364个嗜肺军团菌基因组的序列及分析结果,其中包括来自5种与疾病相关的序列类型的337个基因组,以及代表物种多样性的27个基因组。系统发育分析表明,这5种序列类型在一个高度多样化的物种中具有独立的起源。从头突变的数量极低,最大成对单核苷酸多态性(SNP)范围从19(ST47)到127(ST1),这表明它们是在上个世纪出现的。地理上相距遥远的分离株仅相差少数几个SNP,这表明其传播速度很快。这5种序列类型最近一直在发生重组,导致形成了一个等位基因变体共享库,这可能有助于它们增加致病倾向。最古老的克隆株ST1已在全球传播;在1940年至2000年期间,欧洲出现了4个新的克隆株,它们表现出远距离、快速传播。对于一种传统上被认为是机会性病原体的环境细菌而言,很大一部分临床病例是由最近出现且在国际上传播的、通过趋同进化联系在一起的克隆株引起的,这令人惊讶。为了同时解释其近期出现、快速传播和增加的疾病关联性,我们推测这些序列类型已经适应了新的人造环境生态位,这可能与人类感染和传播有关。