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Development of a Rapid PCR Assay Specific for Staphylococcus saprophyticus and Application to Direct Detection from Urine Samples

机译:快速开发针对腐生葡萄球菌的快速PCR检测方法的开发及其在尿液样品中直接检测的应用

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摘要

Staphylococcus saprophyticus is one of the most frequently encountered microorganisms associated with acute urinary tract infections (UTIs) in young, sexually active female outpatients. Conventional identification methods based on biochemical characteristics can efficiently identify S. saprophyticus, but the rapidities of these methods need to be improved. Rapid and direct identification of this bacterium from urine samples would be useful to improve time required for the diagnosis of S. saprophyticus infections in the clinical microbiology laboratory. We have developed a PCR-based assay for the specific detection of S. saprophyticus. An arbitrarily primed PCR amplification product of 380 bp specific for S. saprophyticus was sequenced and used to design a set of S. saprophyticus-specific PCR amplification primers. The PCR assay was specific for S. saprophyticus when tested with DNA from 49 gram-positive and 31 gram-negative bacterial species. This assay was also able to amplify efficiently DNA from all 60 strains of S. saprophyticus from various origins tested. This assay was adapted for direct detection from urine samples. The sensitivity levels achieved with urine samples was 19 CFU with 30 cycles of amplification and 0.5 CFU with 40 cycles of amplification. This PCR assay for the specific detection of S. saprophyticus is simple and rapid (approximately 90 min, including the time for urine specimen preparation).
机译:腐生葡萄球菌是年轻的,性活跃的女性门诊患者中与急性尿路感染(UTI)相关的最常见微生物之一。基于生化特征的常规鉴定方法可以有效地鉴定腐生链球菌,但这些方法的快速性有待提高。从尿液样本中快速,直接鉴定该细菌将有助于改善临床微生物学实验室诊断腐生链球菌感染所需的时间。我们已经开发了一种基于PCR的检测腐生链球菌的检测方法。对腐生链球菌特异的380 bp的任意引物PCR扩增产物进行测序,并用于设计一套腐生链球菌特异的PCR扩增引物。当用来自49克阳性和31克阴性细菌的DNA进行检测时,PCR检测对腐生链球菌具有特异性。该测定法还能够有效扩增来自不同来源的腐生葡萄球菌的所有60个菌株的DNA。该测定适用于直接从尿液样品中检测。尿液样品达到的灵敏度水平为19 CFU(30个扩增循环)和0.5 CFU(40个扩增循环)。这种特异性检测腐生链球菌的PCR检测方法简便,快速(约90分钟,包括尿液标本制备时间)。

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