首页> 外文OA文献 >Regulators Encoded in the Escherichia coli Type III Secretion System 2 Gene Cluster Influence Expression of Genes within the Locus for Enterocyte Effacement in Enterohemorrhagic E. coli O157:H7
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Regulators Encoded in the Escherichia coli Type III Secretion System 2 Gene Cluster Influence Expression of Genes within the Locus for Enterocyte Effacement in Enterohemorrhagic E. coli O157:H7

机译:大肠杆菌III型分泌系统2基因簇中编码的调节因子影响肠出血性大肠杆菌O157:H7中肠细胞表面化的基因表达

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摘要

Enterohemorrhagic Escherichia coli (EHEC) O157:H7 subverts host cells through a type III secretion system encoded by the locus for enterocyte effacement (LEE). Genome sequencing of this pathotype revealed the existence of a gene cluster encoding components of a second cryptic type III secretion system, E. coli type III secretion system 2 (ETT2). Recently, we showed that the ETT2 gene cluster is present in whole or in part in the majority of E. coli strains but is unable to encode a functional secretion system in most strains, including EHEC O157:H7. However, here we show that mutational inhibition of two regulatory genes (ECs3720 or etrA and ECs3734 or eivF) from the ETT2 cluster in EHEC O157:H7 leads to greatly increased secretion of proteins encoded by the LEE and to increased adhesion to human intestinal cells. Studies in which transcriptional fusions and microarrays were used indicated that EtrA and EivF exert profound negative effects on gene transcription within the LEE. Consistent with these observations, expression of these regulators in an EHEC O26:H- strain led to suppression of protein secretion under LEE-inducing conditions. These findings provide fresh examples of the influence of mobile genetic elements on regulation of the LEE and of cross talk between type III secretion system gene clusters. In addition, they provide a cautionary tale because they show that the effects of regulatory genes can outlive widespread decay of other genes in a functionally coherent gene cluster, a phenomenon that we have named the “Cheshire cat effect.” It also seems likely that variations in the ETT2 regulator repertoire might account for strain-to-strain variation in secretion of LEE-encoded proteins.
机译:肠出血性大肠杆菌(EHEC)O157:H7通过III型分泌系统破坏宿主细胞,该系统由基因编码的位点用于肠上皮细胞的形成(LEE)。此病态型的基因组测序显示存在一个基因簇,该基因簇编码第二种隐秘III类分泌系统,即E. coli III类分泌系统2(ETT2)。最近,我们表明ETT2基因簇存在于大多数大肠杆菌菌株中,全部或部分存在,但不能编码包括EHEC O157:H7在内的大多数菌株的功能性分泌系统。但是,这里我们显示,来自EHEC O157:H7中ETT2簇的两个调节基因(ECs3720或etrA和ECs3734或eivF)的突变抑制导致LEE编码的蛋白质分泌大大增加,并增加了对人肠道细胞的粘附性。使用转录融合和微阵列的研究表明,EtrA和EivF对LEE内部的基因转录产生深远的负面影响。与这些观察结果一致,在EHEC O26:H-菌株中这些调节剂的表达导致在诱导LEE的条件下抑制蛋白质分泌。这些发现提供了移动遗传元件对LEE调节和III型分泌系统基因簇之间的串扰影响的最新实例。此外,它们还提供了一个警告性的故事,因为它们表明调节基因的作用可以超过功能一致的基因簇中其他基因的广泛衰变,这种现象我们称为“柴郡猫效应”。 ETT2调节子库中的变异似乎也可能解释了LEE编码蛋白分泌中的菌株间差异。

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