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A Real-Time PCR-Based Semi-Quantitative Breakpoint to Aid in Molecular Identification of Urinary Tract Infections

机译:基于实时PCR的半定量断点有助于尿路感染分子鉴定

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摘要

This study presents a novel approach to aid in diagnosis of urinary tract infections (UTIs). A real-time PCR assay was used to screen for culture-positive urinary specimens and to identify the causative uropathogen. Semi-quantitative breakpoints were used to screen for significant bacteriuria (presence of ≥105 CFU/ml of uropathogens) or low-level bacteriuria (containing between 103 and 104 CFU/ml of uropathogens). The 16S rDNA-based assay could identify the most prevalent uropathogens using probes for Escherichia coli, Pseudomonas species, Pseudomonas aeruginosa, Staphylococcus species, Staphylococcus aureus, Enterococcus species and Streptococcus species. 330 urinary specimens were analysed and results were compared with conventional urine culture. Using a PCR Ct value of 25 as semi-quantitative breakpoint for significant bacteriuria resulted in a sensitivity and specificity of 97% and 80%, respectively. In 78% of the samples with monomicrobial infections the assay contained probes to detect the bacteria present in the urine specimens and 99% of these uropathogens was correctly identified. Concluding, this proof-of-concept approach demonstrates that the assay can distinguish bacteriuria from no bacteriuria as well as detect the involved uropathogen within 4 hours after sampling, allowing adequate therapy decisions within the same day as well as drastically reduce consequent urine culturing.
机译:这项研究提出了一种新的方法,以帮助诊断尿路感染(UTIs)。实时荧光定量PCR检测用于筛选培养阳性的尿液标本,并确定引起尿毒症的病因。半定量断点用于筛查显着的细菌尿(尿液病原菌≥10 5 CFU / ml)或低水平的细菌尿(含量在10 3 和10 < sup> 4 CFU / ml的尿路致病菌。基于16S rDNA的测定法可使用大肠杆菌,假单胞菌种,铜绿假单胞菌,葡萄球菌种,金黄色葡萄球菌,肠球菌和链球菌种的探针来鉴定最普遍的尿路致病菌。分析了330个尿液标本,并将结果与​​常规尿液培养进行了比较。使用25的PCR Ct值作为半定量转折点来检测明显的细菌尿症,其敏感性和特异性分别为97%和80%。在78%的具有单微生物感染的样品中,该测定法包含用于检测尿液样本中存在的细菌的探针,并且正确鉴定出了这些尿路致病菌的99%。最后,这种概念验证的方法证明了该检测方法可以区分细菌尿症和无细菌尿症,并在采样后4小时内检测出所涉及的尿路致病菌,从而可以在当天做出适当的治疗决定,并大大减少随后的尿培养。

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