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Characterization of the Escherichia coli O157:H7 Outbreak Strain Whose Shiga Toxin 2 Gene Is Inactivated by IS1203v Insertion

机译:大肠杆菌O157:H7爆发株的志贺毒素2基因通过IS1203v插入被灭活的表征

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References(30) Cited-By(2) A total of 12 enterohemorrhagic Escherichia coli (EHEC) O157:H7 strains were isolated during a recent outbreak in a nursery school in Ehime Prefecture, Japan. These isolates were considered to be derived from a common strain when analyzed using an IS-printing method and pulsed-field gel electrophoresis. PCR analysis revealed that the isolates harbor stx1, stx2, eae, and hlyA. However, assessment of the production of the Stx proteins revealed that these isolates produced Stx1 but not Stx2. We determined their stx2 variants such as stx2c and found that the size of the PCR product was much larger than the expected size. Sequencing of the entire stx2 gene revealed that a 1310-bp fragment was inserted into the coding region of the Stx2A subunit and that the sequences of the insert were identical to those of IS1203v. According to the sequences around the insertion site, additional amino acid residues should be attached at the C-terminus of the A subunit, which may hamper the Stx2 complex formation. Finally, this study also suggested that such an insertion may lead to the misinterpretation of results when screening EHEC isolates for virulence genes by PCR.
机译:参考文献(30)被引(2)在日本爱媛县的一所托儿所最近爆发的期间,共分离出了12株肠出血性大肠杆菌(EHEC)O157:H7菌株。当使用IS印刷方法和脉冲场凝胶电泳进行分析时,这些分离株被认为是来自普通菌株。 PCR分析表明,分离株带有stx1,stx2,eae和hlyA。但是,对Stx蛋白产生的评估表明,这些分离物产生了Stx1,但没有产生Stx2。我们确定了它们的stx2变体,例如stx2c,发现PCR产物的大小比预期的大小大得多。整个stx2基因的测序表明,一个1310 bp的片段被插入到Stx2A亚基的编码区域中,并且插入的序列与IS1203v的序列相同。根据插入位点周围的序列,应在A亚基的C末端连接其他氨基酸残基,这可能会阻碍Stx2复合物的形成。最后,这项研究还表明,当通过PCR筛选EHEC分离株的毒力基因时,这种插入可能导致对结果的错误解释。

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