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Asymptomatic bacteriuria Escherichia coli strain 83972 carries mutations in the foc locus and is unable to express F1C fimbriae

机译:无症状的细菌性大肠杆菌菌株83972在Foc基因座中突变并且不能表达F1C FIMBRIAE

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Escherichia coli is the most common organism associated with asymptomatic bacteriuria (ABU). In contrast to uropathogenic E. coli (UPEC), which causes symptomatic urinary tract infection (UTI), very little is known about the mechanisms by which these strains colonize the urinary tract. Bacterial adhesion conferred by specific surface-associated adhesins is normally considered as a prerequisite for colonization of the urinary tract. The prototype ABU E. coli strain 83972 was originally isolated from a girl who had carried it asymptomatically for 3?years. This study characterized the molecular status of one of the primary adhesion factors known to be associated with UTI, namely F1C fimbriae, encoded by the foc gene cluster. F1C fimbriae recognize receptors present in the human kidney and bladder. Expression of the foc genes was found to be up-regulated in human urine. It was also shown that although strain 83972 contains a seemingly intact foc gene cluster, F1C fimbriae are not expressed. Sequencing and genetic complementation revealed that the focD gene, encoding a component of the F1C transport and assembly system, was non-functional, explaining the inability of strain 83972 to express this adhesin. The data imply that E. coli 83972 has lost its ability to express this important colonization factor as a result of host-driven evolution. The ancestor of the strain seems to have been a pyelonephritis strain of phylogenetic group B2. Strain 83972 therefore represents an example of bacterial adaptation from pathogenicity to commensalism through virulence factor loss.
机译:大肠杆菌是与无症状细菌(ABU)相关的最常见的生物体。与尿羟致原细大(UPEC)相比,导致症状尿路感染(UTI),对这些菌株定植泌尿道的机制很少。特异性表面相关纸质碱赋予的细菌粘附通常被认为是泌尿道定植的先决条件。原型阿布大肠杆菌菌株83972原本于一个患有3年的女孩孤立了3年。该研究表征了已知与UTI相关的主要粘合因子之一的分子状态,即由FOC基因簇编码的F1C FIMBRIAE。 F1C FIMBRIAE识别人肾和膀胱中存在的受体。发现FoC基因的表达在人尿中升级。还表明,虽然菌株83972含有看似完整的焦化基因簇,但不表达F1C FIMBriae。测序和遗传互补性揭示了对F1C传输和组装系统的组分的焦焦基因是非功能的,解释了菌株83972表达该粘合剂的无能性。数据暗示,由于主机驱动的演化,大肠杆菌83972失去了表达这一重要定植因子的能力。该菌株的祖先似乎是一种肾盂膜发育B2的肾盂炎菌株。因此,应变83972代表通过毒力因子损失来从致病性与共识的细菌适应的实例。

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