Böhm H, Karch H
Institut für Hygiene und Mikrobiologie, Universität Würzburg, Germany.
J Clin Microbiol. 1992 Aug;30(8):2169-72. doi: 10.1128/jcm.30.8.2169-2172.1992.
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.
对来自不同地理位置的大肠杆菌O157:H7菌株进行了基因组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。用XbaI酶切的DNA片段进行脉冲场凝胶电泳,能清楚地将大肠杆菌O157:H7菌株与非产毒的大肠杆菌O157:H19、O157:H43和O157:H45菌株以及其他血清型的产志贺样毒素大肠杆菌菌株区分开来。然而,在大肠杆菌O157:H7菌株中,限制性酶切图谱要么完全相同,要么仅相差几条片段带。因此,在某些情况下,无法区分流行病学上无关的菌株。用与志贺样毒素II序列互补的DNA探针进行杂交实验表明,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,对于单一高度保守的克隆,如大肠杆菌O157:H7,在流行病学调查中,除了DNA指纹分析外,可能还需要进行其他分型技术。