Isogenic Strain of Escherichia coliO157:H7 That Has Lost both Shiga Toxin 1 and 2 Genes

P. Feng, M. Dey, A. Abe, T. Takeda
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引用次数: 63

Abstract

ABSTRACT An Escherichia coli O157:H7 strain isolated from a patient with hemorrhagic colitis was found to exhibit two slightly different colony morphology types on differential medium. Each morphological type, designated TT12A and TT12B, was isolated, and serological testing using various assays confirmed that both strains carried the O157 and the H7 antigens. Biochemical testing showed that the strains had identical profiles on AP120E analysis and, like typical O157:H7 strains, did not ferment sorbitol or exhibit β-glucuronidase activity. Analysis with a multiplex PCR assay showed that TT12B did not carry the gene for either Shiga toxin 1 (Stx1) or Stx2, whereas these genes were present in TT12A and the toxins were produced. Apart from that, both strains carried the +93 gusA mutation, the cluster I ehxA gene for enterohemolysin, and theeae gene for γ-intimin, which are all characteristics of the O157:H7 serotype. Phenotypic assays confirmed that both strains exhibited enterohemolysin activity and the attachment and effacing lesion on HeLa cells. Multilocus enzyme electrophoresis analysis showed that the strains are closely related genetically and belong in the same clonal group. Pulsed-field gel electrophoresis (PFGE) typing ofXbaI-digested genomic DNA revealed that the two strains differed by two bands but shared 90% similarity and clustered in the same clade. All other non-Stx-producing O157:H7 strains examined clustered in a major clade that was distinct from that of Stx-producing O157:H7 strains. The findings that TT12B was identical to TT12A, except for Stx production, and its PFGE profile is also more closely related to that of Stx-producing O157:H7 strains suggest that TT12B was derived from TT12A by the loss of both stx genes.
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丢失志贺毒素1和2基因的大肠杆菌等基因菌株o157:H7
从出血性结肠炎患者分离的大肠杆菌O157:H7菌株在差异培养基上表现出两种略有不同的菌落形态类型。分别分离出TT12A和TT12B两种形态型,采用多种方法进行血清学检测,证实两种菌株均携带O157和H7抗原。生化试验表明,菌株在AP120E分析中具有相同的特征,并且与典型的O157:H7菌株一样,不发酵山梨醇或表现出β-葡萄糖醛酸酶活性。多重PCR分析表明,TT12B不携带志贺毒素1 (Stx1)或Stx2基因,而TT12A中存在这些基因,并产生了毒素。此外,两株菌株均携带+93 gusA突变、I簇肠溶血素ehxA基因和γ-intimin eae基因,均具有O157:H7血清型的特征。表型分析证实,这两种菌株均表现出肠溶血素活性,并对HeLa细胞产生附着和消退损伤。多位点酶电泳分析表明,两株菌株亲缘关系密切,属同一克隆类群。对xbai消化的基因组DNA进行脉冲场凝胶电泳(PFGE)分型,结果显示两株菌株有两个条带不同,但相似性为90%,属于同一进化支。所有其他非产stx的O157:H7菌株都聚集在一个与产stx的O157:H7菌株不同的主要分支中。TT12B与TT12A除产生Stx外基本一致,其PFGE谱也与产生Stx的O157:H7菌株更为接近,这表明TT12B是由TT12A缺失两个Stx基因衍生而来。
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