Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
PLoS Pathog. 2011 Apr;7(4):e1002018. doi: 10.1371/journal.ppat.1002018. Epub 2011 Apr 7.
Citrobacter rodentium is a natural mouse pathogen that causes attaching and effacing (A/E) lesions. It shares a common virulence strategy with the clinically significant human A/E pathogens enteropathogenic E. coli (EPEC) and enterohaemorrhagic E. coli (EHEC) and is widely used to model this route of pathogenesis. We previously reported the complete genome sequence of C. rodentium ICC168, where we found that the genome displayed many characteristics of a newly evolved pathogen. In this study, through PFGE, sequencing of isolates showing variation, whole genome transcriptome analysis and examination of the mobile genetic elements, we found that, consistent with our previous hypothesis, the genome of C. rodentium is unstable as a result of repeat-mediated, large-scale genome recombination and because of active transposition of mobile genetic elements such as the prophages. We sequenced an additional C. rodentium strain, EX-33, to reveal that the reference strain ICC168 is representative of the species and that most of the inactivating mutations were common to both isolates and likely to have occurred early on in the evolution of this pathogen. We draw parallels with the evolution of other bacterial pathogens and conclude that C. rodentium is a recently evolved pathogen that may have emerged alongside the development of inbred mice as a model for human disease.
柠檬酸杆菌是一种天然的鼠病原体,可引起附着和消蚀(AE)病变。它与临床上重要的人类 AE 病原体肠致病性大肠杆菌(EPEC)和肠出血性大肠杆菌(EHEC)具有共同的毒力策略,被广泛用于模拟这种发病途径。我们之前报道了柠檬酸杆菌 ICC168 的全基因组序列,在其中我们发现该基因组显示出许多新进化病原体的特征。在这项研究中,通过 PFGE、分离株变异的测序、全基因组转录组分析以及移动遗传元件的检查,我们发现,与我们之前的假设一致,柠檬酸杆菌的基因组由于重复介导的大规模基因组重组以及噬菌体等移动遗传元件的活跃转座而不稳定。我们还对另一个柠檬酸杆菌菌株 EX-33 进行了测序,结果表明参考菌株 ICC168 代表了该物种,并且大多数失活突变在该病原体的进化早期就已经存在于两个分离株中。我们与其他细菌病原体的进化进行了类比,并得出结论,柠檬酸杆菌是一种最近进化的病原体,可能与近交系小鼠的发展同时出现,作为人类疾病的模型。