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New Simple and Rapid Test for Culture Confirmation of Mycobacterium tuberculosis Complex: a Multicenter Study

机译:结核分枝杆菌复合物培养确认的新的简单快速测试:多中心研究

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摘要

Mycobacterial antigen MPB64 has been identified as a Mycobacterium tuberculoisis complex-specific secretory protein since 1984. Recently, a simple culture confirmation test for M. tuberculosis complex has been developed by using lateral flow immunochromatographic assay (ICA) to detect MPB64 with anti-MPB64 monoclonal antibody. The current multicenter study evaluated the performance of an ICA slide test for MPB64 antigen in the clinical setting. Primary positive cultures from clinical specimens, as well as stock cultures, were tested. Approximately 100 μl of positive liquid culture medium or suspension made from colonies on solid medium was placed into the test well of the plastic slide devise, and the test was read after 15 min. No processing or instrumentation was required. A total of 304 mycobacterial isolates consisting of M. tuberculosis complex (171 isolates) and mycobacteria other than M. tuberculosis (MOTT) complex (133 isolates) belonging to 18 different species were tested. Growth in liquid media (Mycobacteria Growth Indicator Tube [MGIT] and Radiometric 12B), as well as in solid (Löwenstein-Jensen and Middlebrook 7H10 agar) media, was evaluated. Results were compared with those obtained with nucleic acid-based and/or high-pressure liquid chromatography identification. All MOTT were found to be negative on the ICA slide with no cross-reaction. All M. tuberculosis and M. africanum cultures were found to be positive, whereas the results of M. bovis and M. bovis BCG cultures were variable since some of the BCG strains are known to lack MPB64 antigen production. The results did not change with prolonged storage of cultures. This low-tech rapid test with high sensitivity and specificity could provide an alternative to currently available identification methods, particularly for recently introduced nonradiometric liquid culture systems such as MGIT.
机译:自1984年以来,已将分枝杆菌抗原MPB64鉴定为结核分枝杆菌复合物特异性分泌蛋白。最近,已通过使用侧向流免疫色谱法(ICA)开发了一种用于结核分枝杆菌复合物的简单培养确认测试,以使用抗MPB64单克隆抗体检测MPB64。抗体。当前的多中心研究评估了临床上针对MPB64抗原的ICA玻片测试的性能。测试了来自临床标本的原代阳性培养物以及原种培养物。将大约100μl的阳性液体培养基或由固体培养基上的菌落制成的悬浮液放入塑料载玻片装置的测试孔中,并在15分钟后读取测试结果。无需处理或检测。总共测试了304株分枝杆菌,由结核分枝杆菌复合体(171个分离株)和除18个不同物种之外的结核分枝杆菌(MOTT)复合体以外的分枝杆菌组成。评价了液体培养基(分枝杆菌生长指示管[MGIT]和Radiometric 12B)以及固体培养基(Löwenstein-Jensen和Middlebrook 7H10琼脂)的生长。将结果与通过基于核酸和/或高压液相色谱鉴定获得的结果进行比较。发现所有MOTT在ICA载玻片上均为阴性,无交叉反应。发现所有结核分枝杆菌和非洲分枝杆菌培养物均为阳性,而牛分枝杆菌和牛分枝杆菌BCG培养物的结果却是可变的,因为已知某些BCG菌株缺乏MPB64抗原产生。随着培养物的长期保存,结果没有改变。这种具有高灵敏度和特异性的低技术快速测试可以为当前可用的鉴定方法提供替代方法,尤其是对于最近推出的非辐射液体培养系统(例如MGIT)。

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