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Clonal structure and pathogenicity of Shiga-like toxin-producing, sorbitol-fermenting Escherichia coli O157:H-.
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Alteration of the glycolipid binding specificity of the pig edema toxin from globotetraosyl to globotriaosyl ceramide alters in vivo tissue targetting and results in a verotoxin 1-like disease in pigs.猪水肿毒素的糖脂结合特异性从球四糖神经酰胺改变为球三糖神经酰胺,会改变体内组织靶向性,并导致猪出现类志贺毒素1型疾病。
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Whole-cell repetitive element sequence-based polymerase chain reaction allows rapid assessment of clonal relationships of bacterial isolates.基于全细胞重复元件序列的聚合酶链反应可快速评估细菌分离株的克隆关系。
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Expression of A and B subunits of Shiga-like toxin II as fusions with glutathione S-transferase and their potential for use in seroepidemiology.志贺样毒素II A和B亚基与谷胱甘肽S-转移酶融合表达及其在血清流行病学中的应用潜力。
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Evidence that verotoxins (Shiga-like toxins) from Escherichia coli bind to P blood group antigens of human erythrocytes in vitro.有证据表明,大肠杆菌产生的志贺毒素(类志贺毒素)在体外可与人红细胞的P血型抗原结合。
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Sequence heterogeneity of the eae gene and detection of verotoxin-producing Escherichia coli using serotype-specific primers.eae基因的序列异质性以及使用血清型特异性引物检测产志贺毒素大肠杆菌
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Isolation of Vero cytotoxin-producing Escherichia coli serotypes O9ab:H- and O101:H-carrying VT2 variant gene sequences from a patient with haemolytic uraemic syndrome.从一名溶血性尿毒综合征患者中分离出携带VT2变异基因序列的产维罗细胞毒素大肠杆菌血清型O9ab:H-和O101:H- 。
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人源和猪源产志贺样毒素大肠杆菌O101菌株的克隆相关性

Clonal relatedness of Shiga-like toxin-producing Escherichia coli O101 strains of human and porcine origin.

作者信息

Franke S, Harmsen D, Caprioli A, Pierard D, Wieler L H, Karch H

机构信息

Institut für Hygiene und Mikrobiology, Universität Würzburg, Germany.

出版信息

J Clin Microbiol. 1995 Dec;33(12):3174-8. doi: 10.1128/jcm.33.12.3174-3178.1995.

DOI:10.1128/jcm.33.12.3174-3178.1995
PMID:8586696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC228667/
Abstract

Shiga-like toxin (SLT)-producing Escherichia coli (SLTEC) O101 has recently been associated with hemorrhagic colitis and hemolytic-uremic syndrome in humans. In this study, SLTEC O101 strains from humans and pigs were characterized for clonal relatedness by nucleotide sequence analysis of their slt genes, DNA finger-printing of genomic DNA, and determination of virulence factors. The slt genes of five E. coli O101 strains were cloned and sequenced. For all strains, the deduced amino acid sequences of the B subunits were identical to those of the SLT-IIe present in the classical SLTEC O139 strains that cause edema disease in pigs. The A subunit revealed more than 99% homology to that of SLT-IIe. DNA fingerprinting revealed a high degree of genetic relatedness between the human and porcine O101 isolates. None of the O101 strains investigated had virulence factors frequently found in porcine (F107 fimbriae or heat-stable or heat-labile enterotoxins) or human SLTEC strains (eaeA or enterohemorrhagic E. coli hemolysin). The absence of virulence factors typical of SLT-I- and SLT-II-producing E. Coli together with the presence of SLT-IIe, a toxin previously seen only in porcine E. coli, suggests a new pathogenic mechanism for E. coli O101 infection of humans. For diagnostic purposes, we recommend the use of PCR primers and DNA probes complementary to slt-IIe to correctly identify such strains and to further evaluate their role in human diseases.

摘要

产志贺样毒素(SLT)的大肠杆菌(SLTEC)O101最近被认为与人类出血性结肠炎和溶血尿毒综合征有关。在本研究中,通过对来自人和猪的SLTEC O101菌株的slt基因进行核苷酸序列分析、对基因组DNA进行DNA指纹图谱分析以及确定毒力因子,来鉴定它们的克隆相关性。对五株大肠杆菌O101菌株的slt基因进行了克隆和测序。对于所有菌株,B亚基推导的氨基酸序列与在引起猪水肿病的经典SLTEC O139菌株中存在的SLT-IIe的序列相同。A亚基与SLT-IIe的A亚基有超过99%的同源性。DNA指纹图谱显示人和猪的O101分离株之间存在高度的遗传相关性。所研究的O101菌株均未发现猪源(F107菌毛或耐热或不耐热肠毒素)或人源SLTEC菌株(eaeA或肠出血性大肠杆菌溶血素)中常见的毒力因子。缺乏产SLT-I和SLT-II的大肠杆菌典型的毒力因子,同时存在以前仅在猪大肠杆菌中发现的毒素SLT-IIe,提示了大肠杆菌O101感染人类的一种新的致病机制。为了诊断目的,我们建议使用与slt-IIe互补的PCR引物和DNA探针来正确鉴定此类菌株,并进一步评估它们在人类疾病中的作用。