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DNA fingerprinting of Escherichia coli O157:H7 strains by pulsed-field gel electrophoresis.

机译:大肠杆菌O157:H7菌株的DNA指纹图谱通过脉冲场凝胶电泳分析。

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摘要

Pulsed-field gel electrophoresis of genomic DNA was carried out on Escherichia coli O157:H7 strains from different geographic locations to determine its value in an epidemiological survey of O157 infections. Pulsed-field gel electrophoresis of XbaI-digested DNA fragments clearly separated E. coli O157:H7 strains from nontoxigenic E. coli O157:H19, O157:H43, and O157:H45 strains and from Shiga-like-toxin-producing E. coli strains of other serogroups. However, among the E. coli O157:H7 strains, the restriction patterns either were identical or differed only by a few fragment bands. In some cases, it was therefore impossible to distinguish among epidemiologically unrelated strains. Hybridization experiments with a DNA probe complementary to Shiga-like toxin II sequences revealed that the Shiga-like toxin II genes were located on DNA fragments of different lengths. Our data show that for a single highly conserved clone, such as E. coli O157:H7, other typing techniques may need to be performed in addition to DNA fingerprinting in epidemiological surveys.
机译:在来自不同地理位置的大肠杆菌O157:H7菌株上进行了基因组DNA的脉冲场凝胶电泳,以确定其在O157感染的流行病学调查中的价值。 XbaI消化的DNA片段的脉冲场凝胶电泳清楚地将E. coli O157:H7菌株与非毒素O.:H19、O157:H43和O157:H45菌株以及产志贺样毒素的E.coli分离开其他血清群的菌株。但是,在大肠杆菌O157:H7菌株中,限制性酶切模式是相同的或仅在几个片段带上有所不同。因此,在某些情况下,不可能区分与流行病学无关的菌株。用与志贺样毒素II序列互补的DNA探针进行的杂交实验表明,志贺样毒素II基因位于不同长度的DNA片段上。我们的数据表明,对于单个高度保守的克隆,例如大肠杆菌O157:H7,除流行病学调查中的DNA指纹识别外,可能还需要执行其他分型技术。

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