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Haemolysin E- and enterohaemolysin-derived haemolytic activity of O55/O157 strains and other Escherichia coli lineages

机译:O55 / O157菌株和其他大肠杆菌谱系的溶血素E-和Enterohaemolysin衍生的血液解活性

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Among three haemolysins identified thus far in Escherichia coli, alpha-haemolysin (HlyA) is encoded on the pathogenicity islands of extraintestinal pathogenic strains, while enterohaemolysin (EhxA) is encoded on the virulence plasmids of enterohaemorrhagic E. coli (EHEC) strains. In contrast, the gene for haemolysin E (HlyE) is located on the E. coli chromosome backbone and is therefore widely distributed among E. coli strains. However, because hlyE gene expression is repressed by the H-NS protein and because the gene has been disrupted in many strains, its haemolytic activity cannot be detected in wild-type strains by routine screening on blood agar plates. In this study, we found that the HlyE-derived haemolytic activity of enteropathogenic E. coli (EPEC) O55?:?H7 can be detected after anaerobic cultivation on a washed blood agar plate (EHX plate) that is used to detect the production of EhxA. We also found that the haemolytic activity of EHEC O157?:?H7 observed on EHX plates under aerobic and anaerobic growth conditions is derived from EhxA and HlyE, respectively; this differential expression of the two haemolysins occurs at the transcriptional level. Our analysis of 60 E. coli strains of various pathotypes and phylogenies for their repertoires of haemolysin genes, haemolytic phenotypes and hlyE gene sequences revealed that HlyE activity can generally be detected on EHX plates under anaerobic growth conditions if the gene is intact. Furthermore, our results indicate that hlyE gene inactivation occurred in three of the five E. coli lineages (phylogroups A, B1 and B2), which demonstrates phylogroup-specific gene disruption patterns.
机译:在迄今为止在大肠杆菌鉴定的三种溶血蛋白中,α-氧血素(Hlya)被编码在肝癌致病菌株的致病性岛上,而EnterohaeMolysin(EHXA)被编码在EntoHaemorlagic大肠杆菌(EHEC)菌株的毒力质粒上。相反,氧蛋白酶E(Hlye)的基因位于大肠杆菌染色体骨架上,因此广泛分布在大肠杆菌菌株中。然而,由于Hlye基因表达被H-NS蛋白抑制,因为基因在许多菌株中被破坏,因此不能通过血琼脂平板上的常规筛选在野生型菌株中检测其血液溶液活性。在这项研究中,我们发现肠道致病大肠杆菌(EPEC)O55的Hlye衍生的血液解活性?:αH7可在用于检测生产的洗涤的血糖板(EHX板)上的厌氧培养后进行检测ehxa。我们还发现EHEC O157的溶血活性分别观察到在Aerobic和Anaerobic生长条件下的EHX板上观察到的H7分别来自EHXA和HILYE;这种氧蛋白的这种差异表达发生在转录水平。我们分析了60种大肠杆菌的各种病理型和系统生成的肿瘤基因,血溶解表型和Hlye基因序列的分析表明,如果基因完好无损,通常可以在厌氧生长条件下在EHX平板上检测HILYE活性。此外,我们的结果表明Hlye基因失活在五种大肠杆菌谱系中的三个中发生(晶粒组A,B1和B2)中发生,这证明了特异性植物特异性基因破坏模式。

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