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首页> 外文期刊>Indian Journal of Medical Microbiology >Evaluation of multiplex Polymerase chain reaction utilising multiple targets in Mycobacterium tuberculosis direct test negative but culture positive cases: A potential method for enhancing the diagnosis of tuberculosis
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Evaluation of multiplex Polymerase chain reaction utilising multiple targets in Mycobacterium tuberculosis direct test negative but culture positive cases: A potential method for enhancing the diagnosis of tuberculosis

机译:利用结核分枝杆菌直接检测阴性但培养阳性的多个靶点进行多重聚合酶链反应的评估:增强结核病诊断的潜在方法

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Purpose: To evaluate multiplex Polymerase Chain Reaction (MPCR) utilising multiple targets (IS6110, Protein b [Pab] and MPB64 genes) in Mycobacterium tuberculosis Direct Test (MTD) negative but culture positive cases and comparison of MPCR with Real-Time polymerase chain reaction (RT-PCR) for diagnosis of tuberculosis. Materials and Methods: MPCR was carried out on 28 culture positive sputum samples. Out of 28 culture positive samples, 17 were originally reported, as MTD test negative and 11 were MTD test positive, respectively. The results of MPCR were compared with RT-PCR. To check the specificity of the tests, MPCR and RT-PCR were also evaluated with 16 non-tuberculous mycobacterial (NTM) isolates. Results: Out of 28 culture positive sputum samples, MPCR was positive in all 28/28 samples, whereas RT-PCR was positive in 27/28 samples and MTD test was originally tested positive in six sputum samples and on repeating MTD testing, five more sputum samples were positive and thus total number of MTD positive were 11/28 sputum samples, respectively. All the tests were negative on evaluation with all the 16 NTMs, thus giving specificity of 100% to all the tests; sensitivity of MPCR, RT-PCR and MTD tests were 100%, 96.42% and 39.28%, respectively, in these specifically selected samples. Conclusions: MPCR may be an important tool in the rapid diagnosis of tuberculosis especially in disease endemic, resource limited countries.
机译:目的:利用结核分枝杆菌直接检测(MTD)阴性但培养阳性的多个靶标(IS6110,蛋白b [Pab]和MPB64基因)评估多重聚合酶链反应(MPCR),并将其与实时聚合酶链反应进行比较(RT-PCR)诊断肺结核。材料与方法:对28份培养阳性痰标本进行MPCR。在28个培养阳性样品中,最初报告了17个,因为MTD测试阴性,而11个是MTD测试阳性。将MPCR的结果与RT-PCR进行比较。为了检查测试的特异性,还用16种非结核分枝杆菌(NTM)分离株评估了MPCR和RT-PCR。结果:在28个培养阳性痰样本中,所有28/28样本中MPCR呈阳性,而RT-PCR在27/28样本中呈阳性,最初MTD测试在6个痰样本中呈阳性,并且在重复MTD测试时,另外5个痰标本呈阳性,因此MTD阳性总数分别为11/28。所有测试对16个NTM的评估均为阴性,因此对所有测试的特异性为100%;在这些特别选择的样品中,MPCR,RT-PCR和MTD检测的敏感性分别为100%,96.42%和39.28%。结论:MPCR可能是快速诊断结核病的重要工具,特别是在疾病流行,资源有限的国家。

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