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志贺样毒素II的变体是溶血性尿毒症综合征患者来源的大肠杆菌O157菌株中的主要毒素成分。

Variants of Shiga-like toxin II constitute a major toxin component in Escherichia coli O157 strains from patients with haemolytic uraemic syndrome.

作者信息

Rüssmann H, Schmidt H, Heesemann J, Caprioli A, Karch H

机构信息

Institut für Hygiene und Mikrobiologie, Universität Würzburg, Germany.

出版信息

J Med Microbiol. 1994 May;40(5):338-43. doi: 10.1099/00222615-40-5-338.

Abstract

The prevalence and genotype of Shiga-like toxins (SLTs) in Escherichia coli (O)157 strains from patients in Germany with haemolytic uraemic syndrome (HUS) were investigated. This was done by PCR amplification of the B-subunit genes with two primer pairs--one complementary to slt-IB, and the other homologous to both slt-IIB and slt-IIvB sequences. To distinguish between slt-II and slt-IIv, the amplified DNA was digested with restriction endonucleases HaeIII and FokI. Of the 38 strains examined, 17 harboured sequences for slt-IIv; four contained only slt-IIv, three carried both slt-IIv and slt-I, and 10 strains had slt-IIv and slt-II. A further three genotypes (slt-I, slt-II, slt-I/slt-II) were found in the remaining 21 strains resulting in a total of six slt genotypes. To determine whether the slt genes were expressed, and whether genotypes correlated with phenotypes, all strains were subjected to cytotoxicity assays and colony ELISA. All 38 strains displayed cytotoxic activity to Vero cells in similar quantities. The SLT-I-specific monoclonal antibody (MAb)13C4 reacted with all 10 strains in which slt-I sequences were identified. Colony blot ELISA with the SLT-II specific MAb11E10 detected 27 of 28 strains with slt-II sequences, but did not react with any of the seven strains that carried slt-IIv, or slt-I and slt-IIv. The high SLT variability shown here has diagnostic implications and may well have consequences for the host response in infections associated with these pathogens.

摘要

对德国溶血尿毒综合征(HUS)患者的大肠杆菌(O)157菌株中志贺样毒素(SLTs)的流行情况和基因型进行了调查。通过使用两对引物对B亚基基因进行PCR扩增来完成此项调查,一对引物与slt-IB互补,另一对引物与slt-IIB和slt-IIvB序列同源。为了区分slt-II和slt-IIv,用限制性内切酶HaeIII和FokI对扩增的DNA进行消化。在所检测的38株菌株中,17株含有slt-IIv序列;4株仅含有slt-IIv,3株同时携带slt-IIv和slt-I,10株含有slt-IIv和slt-II。在其余21株菌株中发现了另外三种基因型(slt-I、slt-II、slt-I/slt-II),总共产生了六种slt基因型。为了确定slt基因是否表达,以及基因型是否与表型相关,对所有菌株进行了细胞毒性试验和菌落ELISA。所有38株菌株对Vero细胞均表现出相似数量的细胞毒性活性。SLT-I特异性单克隆抗体(MAb)13C4与所有鉴定出slt-I序列的10株菌株发生反应。用SLT-II特异性MAb11E10进行的菌落印迹ELISA检测到28株含有slt-II序列的菌株中的27株,但未与携带slt-IIv或slt-I和slt-IIv的7株菌株中的任何一株发生反应。此处显示的高SLT变异性具有诊断意义,并且很可能对与这些病原体相关的感染中的宿主反应产生影响。

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