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The place of electrolyte studies in surgical patients.电解质研究在外科患者中的地位。
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2
Shiga toxin activatable by intestinal mucus in Escherichia coli isolated from humans: predictor for a severe clinical outcome.从人类分离出的大肠杆菌中可被肠道黏液激活的志贺毒素:严重临床结局的预测指标。
Clin Infect Dis. 2006 Nov 1;43(9):1160-7. doi: 10.1086/508195. Epub 2006 Oct 2.
3
Rapid identification and differentiation of clinical isolates of enteropathogenic Escherichia coli (EPEC), atypical EPEC, and Shiga toxin-producing Escherichia coli by a one-step multiplex PCR method.通过一步多重聚合酶链反应方法快速鉴定和区分致病性大肠杆菌(EPEC)、非典型EPEC和产志贺毒素大肠杆菌的临床分离株。
J Clin Microbiol. 2006 Jul;44(7):2626-9. doi: 10.1128/JCM.00895-06.
4
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FEMS Microbiol Lett. 2006 Jan;254(1):12-8. doi: 10.1111/j.1574-6968.2005.00005.x.
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Shiga toxin 2e-producing Escherichia coli isolates from humans and pigs differ in their virulence profiles and interactions with intestinal epithelial cells.从人类和猪身上分离出的产志贺毒素2e大肠杆菌菌株在毒力特征以及与肠道上皮细胞的相互作用方面存在差异。
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6
Pigeons as a possible reservoir of Shiga toxin 2f-producing Escherichia coli pathogenic to humans.鸽子可能是对人类致病的产志贺毒素2f大肠杆菌的宿主。
Berl Munch Tierarztl Wochenschr. 2005 Nov-Dec;118(11-12):464-70.
7
Molecular profiling and phenotype analysis of Escherichia coli O26:H11 and O26:NM: secular and geographic consistency of enterohemorrhagic and enteropathogenic isolates.大肠杆菌O26:H11和O26:NM的分子谱分析及表型分析:肠出血性和肠致病性分离株的长期及地理一致性
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Occurrence of hlyA and sheA genes in extraintestinal Escherichia coli strains.肠外大肠杆菌菌株中hlyA和sheA基因的存在情况。
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9
Enteropathogenic and enterohemorrhagic Escherichia coli infections: translocation, translocation, translocation.肠道致病性和肠出血性大肠杆菌感染:易位,易位,易位。
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10
Pathogenesis of Afa/Dr diffusely adhering Escherichia coli.Afa/Dr弥漫性黏附大肠杆菌的发病机制。
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通过使用新型单步多重PCR鉴定表达中等毒力因子谱的非常规肠道致病性大肠杆菌分离株。

Identification of unconventional intestinal pathogenic Escherichia coli isolates expressing intermediate virulence factor profiles by using a novel single-step multiplex PCR.

作者信息

Müller Daniel, Greune Lilo, Heusipp Gerhard, Karch Helge, Fruth Angelika, Tschäpe Helmut, Schmidt M Alexander

机构信息

Institut für Infektiologie, Zentrum für Molekularbiologie der Entzündung (ZMBE), Von-Esmarch-Str. 56, D-48149 Münster, Germany.

出版信息

Appl Environ Microbiol. 2007 May;73(10):3380-90. doi: 10.1128/AEM.02855-06. Epub 2007 Mar 30.

DOI:10.1128/AEM.02855-06
PMID:17400780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1907121/
Abstract

Intestinal pathogenic Escherichia coli represents a global health problem for mammals, including humans. At present, diarrheagenic E. coli bacteria are grouped into seven major pathotypes that differ in their virulence factor profiles, severity of clinical manifestations, and prognosis. In this study, we developed and evaluated a one-step multiplex PCR (MPCR) for the straightforward differential identification of intestinal pathotypes of E. coli. The specificity of this novel MPCR was validated by using a subset of reference strains and further confirmed by PCR-independent pheno- and genotypic characterization. Moreover, we tested 246 clinical E. coli isolates derived from diarrhea patients from several distinct geographic regions. Interestingly, besides strains belonging to the defined and well-described pathotypes, we identified five unconventional strains expressing intermediate virulence factor profiles. These strains have been further characterized and appear to represent intermediate strains carrying genes and expressing factors associated with enteropathogenic E. coli, Shiga toxin-producing E. coli, enterotoxigenic E. coli, and enteroaggregative E. coli alike. These strains represent further examples of the extraordinary plasticity of the E. coli genome. Moreover, this implies that the important identification of specific pathotypes has to be based on a broad matrix of indicator genes. In addition, the presence of intermediate strains needs to be accounted for.

摘要

肠道致病性大肠杆菌是包括人类在内的哺乳动物面临的一个全球性健康问题。目前,致泻性大肠杆菌被分为七种主要致病型,它们在毒力因子谱、临床表现严重程度和预后方面存在差异。在本研究中,我们开发并评估了一种一步多重PCR(MPCR)方法,用于直接鉴别大肠杆菌的肠道致病型。通过使用一组参考菌株验证了这种新型MPCR的特异性,并通过独立于PCR的表型和基因型鉴定进一步确认。此外,我们检测了来自几个不同地理区域腹泻患者的246株临床大肠杆菌分离株。有趣的是,除了属于已定义和充分描述的致病型的菌株外,我们还鉴定出五株表达中间毒力因子谱的非传统菌株。这些菌株已得到进一步鉴定,似乎代表了携带与肠致病性大肠杆菌、产志贺毒素大肠杆菌、肠毒素性大肠杆菌和肠聚集性大肠杆菌相关基因并表达相关因子的中间菌株。这些菌株是大肠杆菌基因组具有非凡可塑性的进一步例证。此外,这意味着特定致病型的重要鉴定必须基于广泛的指示基因矩阵。此外,还需要考虑中间菌株的存在。