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用于鉴定产志贺样毒素大肠杆菌的寡核苷酸探针的评估

Evaluation of oligonucleotide probes for identification of shiga-like-toxin-producing Escherichia coli.

作者信息

Karch H, Meyer T

机构信息

Institut für Medizinische Mikrobiologie und Immunologie, Universitätskrankenhaus Eppendorf, Universität Hamburg, Federal Republic of Germany.

出版信息

J Clin Microbiol. 1989 Jun;27(6):1180-6. doi: 10.1128/jcm.27.6.1180-1186.1989.

Abstract

Four synthetic oligonucleotide probes representing different regions of the Shiga-like toxin I (SLT-I) structural genes and one oligonucleotide derived from the SLT-II gene of Escherichia coli serotype O157:H7 strain 933 were examined for the identification of E. coli strains that produce cytotoxins for Vero or HeLa cells. E. coli strains that synthesize SLT-I alone or O157:H7 isolates that coexpress SLT-I and SLT-II hybridized with all four probes that were complementary to the SLT-I genes, suggesting that they have toxin genes with great homology in all the regions examined. In colony hybridization tests, these oligonucleotide probes did not react with E. coli strains that were nontoxigenic for Vero cells or that produced cytotoxins belonging to the SLT-II family. The probe derived from the slt-IIA gene distinguished E. coli strains that produced SLT-II alone from SLT-I-producing strains and hybridized to all E. coli O157:H7 strains that produced both SLT-I and SLT-II. Using two of these oligonucleotide probes that were complementary to slt-IA or slt-IIA sequences, we identified 50 of 52 cytotoxin-producing strains, whereas none of 416 nontoxigenic E. coli strains was reactive. The colony blot hybridization with the oligonucleotide probes described here can serve as a specific and sensitive test with potential diagnostic value.

摘要

检测了代表志贺样毒素I(SLT-I)结构基因不同区域的四种合成寡核苷酸探针以及一种源自大肠杆菌O157:H7血清型933菌株SLT-II基因的寡核苷酸,以鉴定能产生针对Vero或HeLa细胞的细胞毒素的大肠杆菌菌株。单独合成SLT-I的大肠杆菌菌株或同时表达SLT-I和SLT-II的O157:H7分离株与所有四种与SLT-I基因互补的探针杂交,这表明它们在所检测的所有区域都具有高度同源的毒素基因。在菌落杂交试验中,这些寡核苷酸探针与对Vero细胞无毒性或产生属于SLT-II家族细胞毒素的大肠杆菌菌株不发生反应。源自slt-IIA基因的探针可区分单独产生SLT-II的大肠杆菌菌株和产生SLT-I的菌株,并与所有同时产生SLT-I和SLT-II的大肠杆菌O157:H7菌株杂交。使用其中两种与slt-IA或slt-IIA序列互补的寡核苷酸探针,我们在52株产生细胞毒素的菌株中鉴定出50株,而416株无毒性的大肠杆菌菌株均无反应。本文所述的寡核苷酸探针进行的菌落印迹杂交可作为一种具有潜在诊断价值的特异性和灵敏性检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0abe/267523/dec532289296/jcm00066-0058-a.jpg

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