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Evolutionary analysis and distribution of type III effector genes in pathogenic Escherichia coli from human, animal and food sources

机译:人类,动物和食物来源致病性大肠杆菌中III型效应基因的进化分析和分布

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Molecular analysis of Shiga toxin-producing Escherichia coli (STEC) from different sources is considered as a major approach to assess their risk potential. However, only limited data are available about the correlation of evolutionary relationship, the presence of major virulence factor genes and the putative risk of an STEC strain for human infection. In this study, we analysed the evolutionary relationship of 136 pathogenic E. coli strains from human, animal and food sources by multi-locus sequence typing (MLST) and molecular subtyping of their Shiga toxin (stx) and intimin (eae) genes. Moreover, the distribution of three type III effector genes, encoded within the locus of enterocyte effacement (LEE), and 16 effector genes, which are encoded outside the LEE, was analysed. One hundred and five strains from different sources harboured 5-15 of the analysed non-LEE-encoded effector genes. In 101 of these strains, the LEE genes eae, map, espF and espG were present simultaneously. Thirty-one isolates deriving mainly from food and patients suffering from haemolytic uraemic syndrome (HUS) were eae-negative and did not carry any of the analysed effector genes. By combination of MLST and virulence gene data, we defined five genetic clusters. Within these clusters a clear-cut affiliation of particular sequence types and the occurrence of certain effector genes was observed. However, in contrast to other studies, a significant correlation between the amount and type of effector genes and the risk to cause HUS could not be demonstrated.
机译:从不同来源对产志贺毒素的大肠杆菌(STEC)进行分子分析被认为是评估其潜在风险的主要方法。但是,关于进化关系的相关性,主要毒力因子基因的存在以及STEC株对人类感染的推定风险的可用数据有限。在这项研究中,我们通过多位点序列分型(MLST)以及其志贺毒素(stx)和内膜素(eae)基因的分子亚型分析了人类,动物和食物来源的136种致病性大肠杆菌菌株的进化关系。此外,分析了在肠上皮细胞受损(LEE)基因座内编码的三种III型效应基因和在LEE外编码的16种效应基因的分布。来自不同来源的一百零五个菌株含有5-15个分析的非LEE编码效应基因。在这些菌株中的101个中,LEE基因eae,map,espF和espG同时存在。 31种主要来源于食物的分离株以及患有溶血性尿毒症综合征(HUS)的患者均为eae阴性,并且不携带任何已分析的效应子基因。通过结合MLST和毒力基因数据,我们定义了五个遗传簇。在这些簇中,观察到特定序列类型的明确关联和某些效应基因的出现。但是,与其他研究相比,效应基因的数量和类型与引起HUS的风险之间没有显着的相关性。

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