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Comparison between Culture and a Multiplex Quantitative Real-Time Polymerase Chain Reaction Assay Detecting Ureaplasma urealyticum and U. parvum

机译:检测解脲脲原体和细小支原体的培养物和多重实时定量聚合酶链反应分析方法的比较

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摘要

A novel multiplex quantitative real-time polymerase chain reaction (qPCR) for simultaneous detection of U. urealyticum and U. parvum was developed and compared with quantitative culture in Shepard's 10 C medium for ureaplasmas in urethral swabs from 129 men and 66 women, and cervical swabs from 61 women. Using culture as the gold standard, the sensitivity of the qPCR was 96% and 95% for female urethral and cervical swabs, respectively. In male urethral swabs the sensitivity was 89%. The corresponding specificities were 100%, 87% and 99%. The qPCR showed a linear increasing DNA copy number with increasing colour-changing units. Although slightly less sensitive than culture, this multiplex qPCR assay detecting U. urealyticum and U. parvum constitutes a simple and fast alternative to the traditional methods for identification of ureaplasmas and allows simultaneous species differentiation and quantitation in clinical samples. Furthermore, specimens overgrown by other bacteria using the culture method can be evaluated in the qPCR.
机译:开发了一种同时检测解脲脲原体和细小U.parvum的新型多重定量实时聚合酶链反应(qPCR),并将其与Shepard的10 C培养基中129名男性和66名女性以及宫颈上的尿道拭子中的脲原体的定量培养进行了比较。有61位女性拭子。以培养物为金标准,qPCR对女性尿道拭子和宫颈拭子的敏感性分别为96%和95%。在男性尿道拭子中,敏感性为89%。相应的特异性为100%,87%和99%。 qPCR显示线性增加的DNA拷贝数和增加的变色单元。尽管灵敏度不及培养物,该检测q解脲脲原体和parvum的多重qPCR分析方法构成了传统的鉴定脲原体的方法的简单快速替代方法,可同时对临床样品进行物种分化和定量分析。此外,可以在qPCR中评估使用培养方法被其他细菌长满的标本。

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