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Genus Level Identification of Mycobacteria from Clinical Specimens by Using an Easy-To-Handle Mycobacterium-Specific PCR Assay

机译:通过使用易于处理的分枝杆菌特异性PCR检测法从临床标本中鉴定分枝杆菌属

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摘要

An easy-to-handle Mycobacterium-specific PCR assay for detection of the presence of a wide range of mycobacterial species in clinical samples was evaluated. The performance of the genus probe was compared with the performance of probes specific for Mycobacterium tuberculosis and Mycobacterium avium and with that of standard culture. In addition, the utility of an internal control in monitoring amplification inhibitors was studied. Of 545 respiratory and 325 nonrespiratory specimens (a total of 870 specimens), 58 (6.7%) showed the presence of amplification inhibitors, as determined by a negative result for the internal control. Of these 58 specimens, 31 (53%) were stool specimens; other material, even citrate blood after lysis of erythrocytes, did not pose a problem with regard to inhibition of PCR amplification. Eighty-one of the remaining 812 specimens had a positive Mycobacterium culture result. Of these culture-positive specimens, 58 (71.6%) showed a positive result with the Mycobacterium genus-specific probe. Seventy-two samples had a positive result with the Mycobacterium-specific probe but a negative culture result. Of these 72 samples, 26 samples were regarded as true positive, either because the M. tuberculosis- or M. avium-specific probe was also positive at the same time or because other specimens from the same patient taken at the same time were culture positive. The sensitivity of the Mycobacterium-specific probe was 78.5% and the specificity was 93.5%. This study showed that pretesting of clinical specimens for mycobacteria to the genus level with a Mycobacterium-specific probe offers the routine clinical laboratory the possibility of detecting tuberculous and nontuberculous mycobacteria with one test. Furthermore, specimens testing positive with the genus-specific probe can be immediately identified with species-specific probes.
机译:评估了一种易于操作的分枝杆菌特异性PCR检测方法,用于检测临床样品中多种分枝杆菌物种的存在。将属探针的性能与针对结核分枝杆菌和鸟分枝杆菌的特异性探针的性能以及与标准培养物的性能进行了比较。另外,还研究了内部控制在监测扩增抑制剂中的用途。在545个呼吸道标本和325个非呼吸道标本(总共870个标本)中,有58个(6.7%)显示出存在扩增抑制剂,这是由内部对照的阴性结果确定的。在这58个标本中,有31个(53%)是粪便标本。其他物质,即使是红细胞溶解后的柠檬酸盐血液,在抑制PCR扩增方面也没有问题。其余812个标本中有81个分枝杆菌培养结果为阳性。在这些培养阳性样本中,有58(71.6%)分枝杆菌属特异性探针显示阳性结果。 72个样品的分枝杆菌特异性探针阳性,而培养阴性。在这72个样本中,有26个样本被认为是真正的阳性,这是因为结核分枝杆菌或鸟分枝杆菌特异性探针在同一时间也呈阳性,或者因为同一患者同时采集的其他样本为培养阳性。分枝杆菌特异性探针的敏感性为78.5%,特异性为93.5%。这项研究表明,使用分枝杆菌特异性探针将临床标本分枝杆菌进行预测试至属水平,可以为常规临床实验室提供一种检测结核分枝杆菌和非结核分枝杆菌的可能性。此外,可以使用种属特异性探针立即鉴定出用属特异性探针测试呈阳性的标本。

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