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Comparison of Nested-PCR technique and culture method in detection of Mycobacterium tuberculosis from patients suspected to genitourinary tuberculosis

机译:巢式PCR技术与培养方法在怀疑泌尿生殖道结核患者中检测结核分枝杆菌的比较

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The aim of the present study was to evaluate the diagnostic value of nested PCR in genitourinary tuberculosis (GUTB) compared with acid fast staining and culture method. In total 200 urine samples from suspected cases of GUTB were collected during the period of study. Urine pellets were used for smear preparation, culture and DNA extraction by ether- chloroform method. Nested PCR was performed according to standard protocol using primers based on IS6110 gene fragment. The results obtained by PCR were compared with those obtained by standard acid-fast bacilli stain and culture method. Based on obtained results, the positivity rate of urine samples in this study was 5.0% by using culture and PCR methods and 2.5% for acid fast staining. Four out of total samples showed positive results in all three methods (2%). The sensitivity of PCR in this study was estimated as high as culture equal to 100%, while the sensitivity for direct smear staining was 41.6%. In conclusion, the obtained rate of GUTB in our study was 5.0%. Since the detection rate of culture and nested PCR was identical, we could suggest PCR as a rapid alternative to culture especially for confirmed cases of GUTB.
机译:本研究的目的是评估巢式PCR与耐酸染色和培养方法相比在泌尿生殖系统结核(GUTB)中的诊断价值。在研究期间,总共从疑似GUTB病例中收集了200个尿液样本。尿液沉淀用于涂片制备,培养和通过乙醚-氯仿法提取DNA。使用基于IS6110基因片段的引物,根据标准方案进行巢式PCR。将通过PCR获得的结果与通过标准耐酸杆菌染色和培养方法获得的结果进行比较。根据获得的结果,本研究中使用培养和PCR方法的尿液样本阳性率为5.0%,耐酸染色的阳性率为2.5%。在所有三种方法中,有四个样本显示阳性结果(2%)。在这项研究中,PCR的敏感性估计高达100%,而直接涂片染色的敏感性为41.6%。综上所述,本研究中GUTB的获得率为5.0%。由于培养物和巢式PCR的检测率是相同的,因此我们建议将PCR作为培养物的快速替代方法,特别是对于确诊的GUTB病例。

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