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Comparison of Roche Cobas Amplicor Mycobacterium tuberculosis Assay with In-House PCR and Culture for Detection of M. tuberculosis

机译:罗氏Cobas Amplicor结核分枝杆菌测定与室内PCR和培养物检测结核分枝杆菌的比较

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摘要

The new Roche Cobas Amplicor Mycobacterium tuberculosis assay, which is a semiautomated version of the manually performed Roche Amplicor M. tuberculosis test, was compared to culture and an IS6110-based in-house PCR protocol. A total of 1,681 specimens from 833 patients, including specimen types other than sputum, were tested in parallel by both the in-house PCR and the Cobas Amplicor M. tuberculosis assay. After we resolved discrepant PCR results, the sensitivity, specificity, and positive and negative predictive values for the Cobas Amplicor M. tuberculosis assay were 66.33, 99.71, 94.36, and 97.66%, respectively. The corresponding values for the in-house PCR were 91.08, 99.85, 97.87, and 99.37%, respectively. For culture- and smear-positive specimens, the sensitivity of the Cobas Amplicor M. tuberculosis test was 96.42% (in-house PCR, 100%). If only smear-negative sputum specimens were considered, the Cobas Amplicor M. tuberculosis assay exhibited a sensitivity of 45.45% (in-house PCR, 63.63%) relative to that of culture. With a modified protocol for DNA extraction (washing of samples plus ultrasonication), both PCR methods performed better with gastric aspirates than with sputum samples (sensitivity of the Cobas Amplicor M. tuberculosis assay with smear-negative gastric aspirates, 70.00%; sensitivity of in-house PCR, 90.00%). With dithiothreitol being used for liquefaction of specimens in this study, the Cobas Amplicor M. tuberculosis assay exhibited an inhibition rate of 9.16%. In our view, the new Cobas Amplicor M. tuberculosis test (i) is well suited for typing of smear-positive specimens, (ii) may also be applied to gastric aspirates and other types of specimens if DNA extraction methods are modified appropriately, and (iii) exhibits a sensitivity with smear-negative sputum specimens which makes it recommendable that a minimum of three samples from the same patient be tested.
机译:新的Roche Cobas Amplicor结核分枝杆菌测定法是人工进行的Roche Amplicor结核分枝杆菌检验的半自动化版本,与培养和基于IS6110的内部PCR方案进行了比较。通过内部PCR和Cobas Amplicor结核分枝杆菌检测,对833位患者的1,681份标本进行了平行检测,包括除痰以外的其他标本类型。解决差异PCR结果后,Cobas Amplicor结核分枝杆菌测定的灵敏度,特异性和阳性和阴性预测值分别为66.33、99.71、94.36和97.66%。内部PCR的相应值分别为91.08、99.85、97.87和99.37%。对于培养和涂片阳性的标本,Cobas Amplicor结核分枝杆菌试验的灵敏度为96.42%(室内PCR为100%)。如果仅考虑涂片阴性痰标本,则Cobas Amplicor结核分枝杆菌测定法相对于培养物的灵敏度为45.45%(室内PCR为63.63%)。通过改良的DNA提取方案(样品洗涤和超声处理),两种PCR方法对胃吸出物的效果均优于对痰样品(Cobas Amplicor M.结核病涂片阴性胃吸出物的灵敏度为70.00%;对内部PCR,90.00%)。在这项研究中,以二硫苏糖醇用于标本的液化,Cobas Amplicor结核分枝杆菌测定法显示抑制率为9.16%。我们认为,新的Cobas Amplicor结核分枝杆菌试验(i)非常适合于对涂片阳性样本进行分型,(ii)如果DNA提取方法经过适当修改,也可应用于胃吸出物和其他类型的样本,以及(iii)对涂片阴性的痰标​​本表现出敏感性,因此建议至少测试来自同一患者的三个样本。

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