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Simple and rapid method for detection of nitrate reductase activity of Mycobacterium tuberculosis and Mycobacterium canettii grown in the Bactec MGIT960 system

机译:Bactec MGIT960系统中生长的结核分枝杆菌和canettii结核分枝杆菌硝酸还原酶活性的简便快速检测方法

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摘要

Mycobacterium tuberculosis reduces nitrate very strongly as compared to Mycobacterium bovis and M. bovis BCG. Nitrate reductase, in conjunction with niacin accumulation, constitutes one of the major biochemical tests used in clinical microbiology laboratories to differentiate M. tuberculosis from other members of the M. tuberculosis complex, as well as nontuberculous Mycobacteria. Determination of nitrate reductase activity is currently performed using cultures grown on solid media with a slow detection time and the need for large quantities of bacilli, as otherwise the test is not reliable. Hereby, we propose a nitrate reduction test coupled to Bactec MGIT960 system as a simple, rapid and economic method with a total gain of time of about 3 to 4 weeks over the conventional solid medium. In our study, almost all the M. tuberculosis and Mycobacterium canettii strains gave a strongly positive nitrate reductase result within 1 day of positive detection by the MGIT960 system. In contrast, M. bovis, M. bovis BCG and M. africanum strains remained negative even after 14 days of incubation. The possibility to detect nitrate reductase within 1 to 3 days of a positive culture using MGIT960 opens new perspectives with the possibility of confirming M. tuberculosis starting directly from pathological specimens. (C) 2010 Elsevier B.V. All rights reserved.
机译:与牛分枝杆菌和牛分枝杆菌BCG相比,结核分枝杆菌非常强烈地减少硝酸盐。硝酸还原酶与烟酸积累一起构成了临床微生物学实验室中用于区分结核分枝杆菌与结核分枝杆菌复合体其他成员以及非结核分枝杆菌的主要生化测试之一。目前,硝酸盐还原酶活性的测定是使用在固体培养基上生长的培养物进行的,该培养物的检测时间较慢,并且需要大量杆菌,否则该测试将不可靠。据此,我们提出了一种与Bactec MGIT960系统耦合的硝酸盐还原试验,作为一种简单,快速且经济的方法,与传统的固体培养基相比,总的时间增加了约3-4周。在我们的研究中,几乎所有的结核分枝杆菌和canettii分枝杆菌菌株在MGIT960系统阳性检测后的1天之内都给出了强烈的硝酸还原酶阳性结果。相比之下,即使经过14天的孵育,牛分枝杆菌,牛分枝杆菌BCG和非洲分枝杆菌仍为阴性。使用MGIT960在阳性培养的1至3天内检测到硝酸还原酶的可能性开辟了新的前景,有可能直接从病理标本中确认结核分枝杆菌。 (C)2010 Elsevier B.V.保留所有权利。

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