Han Haihong, Wong Hin-Chung, Kan Biao, Guo Zhaobiao, Zeng Xiaotao, Yin Shengjun, Liu Xiumei, Yang Ruifu, Zhou Dongsheng
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, PR China.
BMC Genomics. 2008 Nov 28;9:570. doi: 10.1186/1471-2164-9-570.
Outbreak of V. parahaemolyticus infections occurred since 1996 was linked to a proposed clonal complex, the pandemic group. The whole genome sequence provides an unprecedented opportunity for dissecting genome plasticity and phylogeny of the populations of V. parahaemolyticus. In the present work, a whole-genome cDNA microarray was constructed to compare the genomic contents of a collection of 174 strains of V. parahaemolyticus.
Genes that present variably in the genome accounted for about 22% of the whole gene pool on the genome. The phylogenetic analysis of microarray data generated a minimum spanning tree that depicted the phylogenetic structure of the 174 strains. Strains were assigned into five complexes (C1 to C5), and those in each complex were related genetically and phylogenetically. C3 and C4 represented highly virulent clinical clones. C2 and C3 constituted two different clonal complexes 'old-O3:K6 clone' and 'pandemic clone', respectively. C3 included all the 39 pandemic strains tested (trh-, tdh+ and GS-PCR+), while C2 contained 12 pre-1996 'old' O3:K6 strains (trh+, tdh- and GS-PCR-) tested herein. The pandemic clone (post-1996 'new' O3:K6 and its derivates O4:K68, O1:K25, O1:KUT and O6:K18) might be emerged from the old-O3:K6 clone, which was promoted by acquisition of toxRS/new sequence and genomic islands. A phylogenetic intermediate O3:K6 clade (trh-, tdh- and GS-PCR+) was identified between the pandemic and old-O3:K6 clones.
A comprehensive overview of genomic contents in a large collection of global isolates from the microarray-based comparative genomic hybridization data enabled us to construct a phylogenetic structure of V. parahaemolyticus and an evolutionary history of the pandemic group (clone) of this pathogen.
自1996年以来发生的副溶血性弧菌感染暴发与一个假定的克隆复合体即大流行群有关。全基因组序列为剖析副溶血性弧菌群体的基因组可塑性和系统发育提供了前所未有的机会。在本研究中,构建了全基因组cDNA微阵列以比较174株副溶血性弧菌的基因组内容。
基因组中可变存在的基因约占基因组全基因库的22%。对微阵列数据的系统发育分析生成了一棵最小生成树,描绘了174株菌株的系统发育结构。菌株被分为五个复合体(C1至C5),每个复合体中的菌株在遗传和系统发育上相关。C3和C4代表高毒力临床克隆。C2和C3分别构成两个不同的克隆复合体“旧O3:K6克隆”和“大流行克隆”。C3包括所有测试的39株大流行菌株(trh-、tdh+和GS-PCR+),而C2包含本文测试的12株1996年前的“旧”O3:K6菌株(trh+、tdh-和GS-PCR-)。大流行克隆(1996年后的“新”O3:K6及其衍生物O4:K68、O1:K25、O1:KUT和O6:K18)可能起源于旧O3:K6克隆,这是通过获得toxRS/new序列和基因组岛而促进的。在大流行克隆和旧O3:K6克隆之间鉴定出一个系统发育中间型O3:K6分支(trh-、tdh-和GS-PCR+)。
基于微阵列的比较基因组杂交数据对大量全球分离株的基因组内容进行全面概述,使我们能够构建副溶血性弧菌的系统发育结构以及该病原体大流行群(克隆)的进化史。