Utility of Real-Time Quantitative Polymerase Chain Reaction in Detecting Mycobacterium tuberculosis

被引:7
|
作者
Lv, Zhongquan [1 ]
Zhang, Mingxin [1 ]
Zhang, Hui [2 ]
Lu, Xinxin [1 ]
机构
[1] Capital Med Univ, Beijing Tongren Hosp, Clin Lab, Beijing 100069, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, TB Control Ctr, Beijing, Peoples R China
关键词
PCR ASSAY; DIFFERENTIATION; IDENTIFICATION; AMPLIFICATION; DIAGNOSIS; CULTURE; SMEAR; DNA;
D O I
10.1155/2017/1058579
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study aimed to assess the value of real-time quantitative polymerase chain reaction (RT-qPCR) for the detection of Mycobacterium tuberculosis (MTB). Samples from 192 patients with suspected MTB were examined by RT-qPCR and an improved Lowenstein-Jensen (L-J) culture method. To evaluate the diagnostic usefulness of RT-qPCR in detecting MTB, a receiver operating characteristic (ROC) curve for RT-qPCR was generated, and the area under the curve (AUC) as well as a cutoff value was calculated. Using the L-J culture method as the gold standard, accuracy of the RT-qPCRmethod for detecting MTB was 92.7%, with sensitivity and specificity of 62.5% and 97.02%, respectively. In comparisonwith the improved L-J culturemethod, the AUC of RT-qPCRROC curve was 0.957, which was statistically significant (p < 0.001). The Youden Index reached the maximum value (0.88) for gene copy number of 794.5 IU/mL, which was used as the cutoff value. RT-qPCR detection of MTB yielded results consistent with those of the improved L-J culture method, with high accuracy. RT-qPCR may be used as an auxiliary method for etiological diagnosis of tuberculosis.
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页数:5
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