评估从尿液中分离出的大肠埃希氏菌株致病潜力的综合方法

Mariia A. Makarova, Z. N. Matveeva, Lidiya A. Kaftyreva
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Detection of 17 genes encoding the synthesis of: adhesins (pap, fimH, sfa, focG, afa), toxins (hlyA, cvaC, cnf, cdtB), capsular antigens (kpsMTII, kpsMTIII, kpsMT K1), siderophores (fyuA, iutA), invasins (ibeA), genetic markers of the pathogenicity island (PAI) of UPEC CFT073, the gene (traT) encoding serum resistance capacity and phylogenetic groups were performed by PCR (CXT-1000, BioRad, USA) with published primers (Synthol, Sibenzyme, Evrogen, Russia). To assess the statistical significance of differences, Fisher's exact test was used. Differences were considered significant at a confidence interval of 95% (p 0.05). \nResults. E. coli strains more often (p 0.05) belonged to the phylogenetic group B2 (57.7%). Pathogenetically significant virulence determinants were identified in 97.9% of strains. Based on the combination of 17 genes, 134 individual virulence genotypes were identified. 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摘要

导言。尿路致病性大肠埃希菌(UPEC)的特点是由于存在特定的毒力因子而能够在泌尿道中存活和繁殖。在常规实验室实践中,检测出具有诊断意义的菌尿并不能说明泌尿系统(肾实质、膀胱)的感染程度、菌株在感染过程的进展和慢性化过程中的致病潜力以及危及生命的情况(尿毒症、脑膜炎)。目标分析从尿液中分离出的大肠杆菌菌株的种群结构、遗传多样性和致病性。材料和方法。研究了从尿液中分离出的 194 株大肠杆菌。检测了 17 个编码合成以下物质的基因:粘附素(pap、fimH、sfa、focG、afa)、毒素(hlyA、cvaC、cnf、cdtB)、荚膜抗原(kpsMTII、kpsMTIII、kpsMT K1)、嗜苷酸(fyuA、iutA)、侵袭素(ibeA)、UPEC CFT073 致病性岛(PAI)的遗传标记、对编码血清抗性能力的基因(traT)和系统发生组的研究是通过 PCR(CXT-1000,BioRad,美国)和已发表的引物(Synthol、Sibenzyme、Evrogen,俄罗斯)进行的。为评估差异的统计学意义,采用了费雪精确检验。在置信区间为 95% 时,差异被认为是显著的(P 0.05)。结果大肠杆菌菌株更多属于系统发育组 B2(57.7%)(p 0.05)。在 97.9% 的菌株中发现了具有重要致病性的毒力决定因子。根据 17 个基因的组合,确定了 134 个毒力基因型。在 93.3% 的菌株中,发现了发生复发性尿路感染(UTIs)的遗传易感性,6.9% 的菌株有发生肾盂肾炎和复发性膀胱炎的可能性。在 12% 的菌株中发现了尿路感染危及生命并发症的标志物,其中 10.7% 出现尿毒症,1.3% 出现脑膜炎。结论在从尿液中分离出的大肠杆菌菌株中检测到复合基因,证实了该分离菌株的病原学意义,并可评估其引发慢性和严重危及生命的并发症的致病潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An integrative approach to assessing the pathogenic potential of Escherichia coli strains isolated from urine
Introduction. Uropathogenic Escherichia coli (UPEC) are characterized by the ability to survive and reproduce in the urinary tract due to the presence of specific virulence factors. In routine laboratory practice, the detection of diagnostically significant bacteriuria does not provide an idea of the level of infection of the urinary system (renal parenchyma, bladder), the pathogenic potential of the strain in the progression and chronicity of the infectious process, and the occurrence of life-threatening conditions (urosepsis, meningitis). Objective. To characterize the population structure, genetic diversity and pathogenic potential of E. coli strains isolated from urine. Materials and methods. 194 strains of E. coli isolated from urine were studied. Detection of 17 genes encoding the synthesis of: adhesins (pap, fimH, sfa, focG, afa), toxins (hlyA, cvaC, cnf, cdtB), capsular antigens (kpsMTII, kpsMTIII, kpsMT K1), siderophores (fyuA, iutA), invasins (ibeA), genetic markers of the pathogenicity island (PAI) of UPEC CFT073, the gene (traT) encoding serum resistance capacity and phylogenetic groups were performed by PCR (CXT-1000, BioRad, USA) with published primers (Synthol, Sibenzyme, Evrogen, Russia). To assess the statistical significance of differences, Fisher's exact test was used. Differences were considered significant at a confidence interval of 95% (p 0.05). Results. E. coli strains more often (p 0.05) belonged to the phylogenetic group B2 (57.7%). Pathogenetically significant virulence determinants were identified in 97.9% of strains. Based on the combination of 17 genes, 134 individual virulence genotypes were identified. In 93.3% of strains, a genetic predisposition to the occurrence of recurrent urinary tract infections (UTIs) was revealed, in 6.9% there was a potential for the development of pyelonephritis and recurrent cystitis. Markers of life-threatening complications of UTI were identified in 12% of strains, of which 10.7% were the development of urosepsis and 1.3% were meningitis. Conclusion. Detection of a complex of genes in E. coli strains isolated from urine confirms the etiological significance of the isolate and allows one to assess the pathogenic potential for the development of chronic and severe life-threatening complications.
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