Takeuchi H, Yamamoto S, Terai A, Kurazono H, Takeda Y, Okada Y, Yoshida O
Department of Urology, Faculty of Medicine, Kyoto University, Japan.
Int J Urol. 1996 May;3(3):202-6. doi: 10.1111/j.1442-2042.1996.tb00517.x.
Urea-splitting microorganisms cannot always be detected by stone or urine culture in patients with infection stones. Detection of genetic elements within the calculi by the polymerase chain reaction (PCR) may be a useful alternative. In this study, we assessed the usefulness of the PCR method in detecting the urease gene specific to Proteus mirabilis in urinary calculi.
Thirty-eight metabolic stones (calcium oxalate and/or calcium phosphate, uric acid, or cystine) and 49 struvite stones were examined. The PCR was applied with DNA extracted by boiling pulverized stone pieces.
Of the 87 stones, PCR demonstrated the presence of the P. mirabilis urease elements ureC1 and ureC2 in 17, all of which were struvite. Stone culture and urine culture had been performed in 22 and 46 struvite stone cases, respectively, and the PCR was positive in all of the 10 culture-positive calculi and also in two calculi from which P. mirabilis was not isolated.
PCR was reliable and convenient for detecting P. mirabilis in desiccated struvite calculi. Study to detect other species such as Ureaplasma or Corynebacterium would be useful in elucidating the role of bacterial infection in the formation of these stones.
在感染性结石患者中,通过结石或尿液培养不一定总能检测到尿素分解微生物。通过聚合酶链反应(PCR)检测结石内的遗传元件可能是一种有用的替代方法。在本研究中,我们评估了PCR方法在检测尿路结石中奇异变形杆菌特异性脲酶基因方面的实用性。
检查了38块代谢性结石(草酸钙和/或磷酸钙、尿酸或胱氨酸)和49块鸟粪石结石。对通过煮沸粉碎的结石碎片提取的DNA进行PCR检测。
在87块结石中,PCR检测显示17块结石中存在奇异变形杆菌脲酶元件ureC1和ureC2,所有这些结石均为鸟粪石。分别对22例和46例鸟粪石结石病例进行了结石培养和尿液培养,在所有10例培养阳性的结石以及2例未分离出奇异变形杆菌的结石中,PCR均呈阳性。
PCR检测干燥鸟粪石结石中的奇异变形杆菌可靠且方便。检测其他菌种如解脲脲原体或棒状杆菌的研究将有助于阐明细菌感染在这些结石形成中的作用。