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首页> 外文期刊>Microbiology >Positive effects of multiple pch genes on expression of the locus of enterocyte effacement genes and adherence of enterohaemorrhagic Escherichia coli O157?:?H7 to HEp-2 cells
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Positive effects of multiple pch genes on expression of the locus of enterocyte effacement genes and adherence of enterohaemorrhagic Escherichia coli O157?:?H7 to HEp-2 cells

机译:多个PCH基因对肠溶性抑制基因座位表达及肠出血rescherichia Coli O157的粘附性的阳性作用及肠溶性大肠杆菌o157的粘附性?:ΔH7至Hep-2细胞

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Enteropathogenic and enterohaemorrhagic Escherichia coli (EPEC and EHEC, respectively) genomes contain a pathogenicity island, termed the locus of enterocyte effacement (LEE), which encodes genes involved in the formation of attaching and effacing lesions on epithelial cells. To elucidate the regulatory mechanism of the LEE genes in EHEC, an EHEC O157 genomic library was screened for clones which modulated expression of the LEE genes. From more than 5000 clones, a DNA fragment was obtained containing a perC homologue as a positive regulator for the LEE genes. In EPEC, perC is known to be part of the per operon, along with perA and perB, located on the EPEC adherence factor plasmid, which is not found in EHEC. However, the complete genome sequence of EHEC O157 Sakai strain reveals that there are five perC-like sequences, but no perA and perB, on the chromosome. These five perC homologues were characterized, and it was found that three of the homologues (renamed perChomologue pchA, pchB and pchC) encoded 104?aa proteins, and when expressed on a multicopy plasmid enhanced the expression of LEE genes. In contrast, perC homologues encoding proteins of 89 and 90?aa, renamed pchD and pchE, respectively, had no significant effect. Deletion mutants of the pch genes were constructed, and the effect on the expression of LEE-encoded type III effector proteins, such as EspA, B and D, and adhesion phenotype to HEp-2 cells was examined. Deletion of pchA or pchB, but not pchC, decreased the expression of Esp proteins and adhesion to HEp-2 cells. Such effects were more apparent with mutants carrying double deletions of pchA/pchB or pchA/pchC, suggesting that pchA/B/C are all necessary for full expression of the LEE genes and adhesion to HEp-2 cells. Further study demonstrated that the positive effect of pchA/B/C was caused by enhanced transcription of the LEE-encoded regulatory gene, ler. Introduction of a multicopy plasmid carrying each pchA/B/C gene significantly induced microcolony formation by EHEC O157 on HEp-2 cells. These results suggest that the pchABC genes are necessary for full virulence of EHEC O157.
机译:肠寄生和Enterohaemorlagic大肠杆菌(分别)基因组(EPEC和EHEC)基因组含有致病性岛,称为肠细胞抑制(LEE)的基因座,其编码涉及在上皮细胞上形成和抑变病变的形成。为了阐明EHEC中LEE基因的调节机制,筛选了一种调节李基因表达的克隆的EHEC O157基因组文库。从5000多个克隆,获得DNA片段,含有PERC同源物作为李基因的阳性调节剂。在EPEC中,已知Perc是每个操纵子的一部分,以及位于EPEC粘附因子质粒上的PERA和PERB,其在EHEC中未发现。然而,EHEC O157 Sakai菌株的完整基因组序列揭示了染色体上有五种Perc样序列,但没有PERA和PERB。这五种完全的同源物的特征在于,发现三种同源物(重命名的Perchomologue PCHA,PCHB和PCHC)编码了104〜A蛋白,并且当在多拷贝质粒上表达时,增强了LEE基因的表达。相反,分别编码89和90的蛋白质的PERC同源物,分别重命名PCHD和PCHE,没有显着效果。构建了PCH基因的缺失突变体,研究了对Lee编码III型效应蛋白的表达的影响,例如ESPA,B和D,以及粘附表型至HEP-2细胞。缺失PCHA或PCHB,但不是PCHC,降低了esp蛋白的表达和对Hep-2细胞的粘附性。由于携带PCHA / PCHB或PCHA / PCHC的双重缺失的突变体更加明显,表明PCHA / B / C是完全表达LEE基因和对HEP-2细胞的粘附性必需的。进一步的研究表明,PCHA / B / C的正效应是由Lee编码的调节基因,LER的增强转录引起的。引入携带每个PCHA / B / C基因的多拷贝质粒显着诱导了EHEC O157在HEP-2细胞上的微胶体形成。这些结果表明,PCHABC基因对于EHEC O157的全毒力是必要的。

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