University of Maryland School of Medicine, Institute for Genome Sciences and Department of Microbiology, Baltimore, USA.
N Engl J Med. 2011 Aug 25;365(8):709-17. doi: 10.1056/NEJMoa1106920. Epub 2011 Jul 27.
A large outbreak of diarrhea and the hemolytic-uremic syndrome caused by an unusual serotype of Shiga-toxin-producing Escherichia coli (O104:H4) began in Germany in May 2011. As of July 22, a large number of cases of diarrhea caused by Shiga-toxin-producing E. coli have been reported--3167 without the hemolytic-uremic syndrome (16 deaths) and 908 with the hemolytic-uremic syndrome (34 deaths)--indicating that this strain is notably more virulent than most of the Shiga-toxin-producing E. coli strains. Preliminary genetic characterization of the outbreak strain suggested that, unlike most of these strains, it should be classified within the enteroaggregative pathotype of E. coli.
We used third-generation, single-molecule, real-time DNA sequencing to determine the complete genome sequence of the German outbreak strain, as well as the genome sequences of seven diarrhea-associated enteroaggregative E. coli serotype O104:H4 strains from Africa and four enteroaggregative E. coli reference strains belonging to other serotypes. Genomewide comparisons were performed with the use of these enteroaggregative E. coli genomes, as well as those of 40 previously sequenced E. coli isolates.
The enteroaggregative E. coli O104:H4 strains are closely related and form a distinct clade among E. coli and enteroaggregative E. coli strains. However, the genome of the German outbreak strain can be distinguished from those of other O104:H4 strains because it contains a prophage encoding Shiga toxin 2 and a distinct set of additional virulence and antibiotic-resistance factors.
Our findings suggest that horizontal genetic exchange allowed for the emergence of the highly virulent Shiga-toxin-producing enteroaggregative E. coli O104:H4 strain that caused the German outbreak. More broadly, these findings highlight the way in which the plasticity of bacterial genomes facilitates the emergence of new pathogens.
一种由产志贺毒素大肠杆菌(O104:H4)的不常见血清型引起的大规模腹泻和溶血性尿毒综合征疫情于 2011 年 5 月在德国爆发。截至 7 月 22 日,已报告大量产志贺毒素大肠杆菌引起的腹泻病例 - 3167 例无溶血性尿毒综合征(16 例死亡)和 908 例溶血性尿毒综合征(34 例死亡) - 表明该菌株的毒力明显高于大多数产志贺毒素大肠杆菌菌株。对疫情菌株的初步遗传特征分析表明,与大多数菌株不同,它应归类于肠聚集型大肠杆菌。
我们使用第三代单分子实时 DNA 测序来确定德国疫情株的全基因组序列,以及来自非洲的 7 株腹泻相关肠聚集型大肠杆菌 O104:H4 血清型菌株和 4 株属于其他血清型的肠聚集型大肠杆菌参考株的基因组序列。使用这些肠聚集型大肠杆菌基因组以及 40 株先前测序的大肠杆菌分离株进行全基因组比较。
肠聚集型大肠杆菌 O104:H4 菌株密切相关,在大肠杆菌和肠聚集型大肠杆菌菌株中形成一个独特的分支。然而,德国疫情株的基因组可以与其他 O104:H4 菌株区分开来,因为它包含编码志贺毒素 2 的噬菌体和一组独特的额外毒力和抗生素耐药性因子。
我们的研究结果表明,水平基因交换允许产生高毒力产志贺毒素肠聚集型大肠杆菌 O104:H4 菌株,该菌株引发了德国疫情。更广泛地说,这些发现强调了细菌基因组的可塑性如何促进新病原体的出现。