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产志贺毒素大肠杆菌菌株肠细胞脱落位点的插入位点定位及致病型确定

Localization of the insertion site and pathotype determination of the locus of enterocyte effacement of shiga toxin-producing Escherichia coli strains.

作者信息

Bertin Yolande, Boukhors Karima, Livrelli Valerie, Martin Christine

机构信息

Laboratoire de Microbiologie, Centre de Recherche INRA de Clermont-Ferrand-Theix, 63122 St-Genès Chapanelle, France.

出版信息

Appl Environ Microbiol. 2004 Jan;70(1):61-8. doi: 10.1128/AEM.70.1.61-68.2004.

Abstract

Of 220 Shiga toxin-producing Escherichia coli (STEC) strains collected in central France from healthy cattle, food samples, and asymptomatic children, 12 possessed the eae gene included in the locus of enterocyte effacement (LEE) pathogenicity island. Based on gene typing, we observed 7 different eae espA espB tir pathotypes among the 12 STEC strains and described the new espAbetav variant. As previously observed, the O157 serogroup is associated with eaegamma, O26 is associated with eaebeta, and O103 is associated with eaeepsilon. However, the unexpected eaezeta allele was detected in 5 of the 12 isolates. PCR amplification and pulsed-field gel electrophoresis using the I-CeuI endonuclease followed by Southern hybridization indicated that the LEE was inserted in the vicinity of the selC (three isolates), pheU (two isolates), or pheV (six isolates) tRNA gene. Six isolates harbored two or three of these tRNA loci altered by the insertion of integrase genes (CP4-int and/or int-phe), suggesting the insertion of additional foreign DNA fragments at these sites. In spite of great genetic diversity of LEE pathotypes and LEE insertion sites, bovine strains harbor alleles of LEE genes that are frequently found in clinical STEC strains isolated from outbreaks and sporadic cases around the world, underscoring the potential risk of the bovine strains on human health.

摘要

在法国中部从健康牛、食品样本和无症状儿童中收集的220株产志贺毒素大肠杆菌(STEC)菌株中,有12株携带位于肠细胞脱落(LEE)致病岛中的eae基因。基于基因分型,我们在12株STEC菌株中观察到7种不同的eae espA espB tir致病型,并描述了新的espAbetav变体。如先前观察到的,O157血清群与eaegamma相关,O26与eaebeta相关,O103与eaeepsilon相关。然而,在12株分离株中有5株检测到意外的eaezeta等位基因。使用I-CeuI内切酶进行PCR扩增和脉冲场凝胶电泳,随后进行Southern杂交,结果表明LEE插入到selC(3株分离株)、pheU(2株分离株)或pheV(6株分离株)tRNA基因附近。6株分离株含有两到三个因整合酶基因(CP4-int和/或int-phe)插入而改变的这些tRNA位点,表明在这些位点插入了额外的外源DNA片段。尽管LEE致病型和LEE插入位点具有很大的遗传多样性,但牛源菌株携带的LEE基因等位基因在从世界各地的暴发和散发病例中分离出的临床STEC菌株中经常出现,这突出了牛源菌株对人类健康的潜在风险。

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