Moore A V, Kirk S M, Callister S M, Mazurek G H, Schell R F
Wisconsin State Laboratory of Hygiene, University of Wisconsin, Madison, Wisconsin 53706, USA.
J Clin Microbiol. 1999 Mar;37(3):479-83. doi: 10.1128/JCM.37.3.479-483.1999.
We showed previously that susceptibility testing for Mycobacterium tuberculosis labeled with fluorescein diacetate could be accomplished rapidly by using flow cytometry. However, safety was a major concern because mycobacteria were not killed prior to flow cytometric analysis. In this study, we developed a biologically safe flow cytometric susceptibility test that depends on detection and enumeration of actively growing M. tuberculosis organisms in drug-free and antimycobacterial agent-containing medium. The susceptibilities of 17 clinical isolates of M. tuberculosis to ethambutol, isoniazid, and rifampin were tested by the agar proportion and flow cytometric methods. Subsequently, all flow cytometric susceptibility test samples were inactivated by exposure to paraformaldehyde before analysis with a flow cytometer. Agreement between the results from the two methods was 98%. In addition, the flow cytometric results were available 72 h after the initiation of testing. The flow cytometric susceptibility assay is safe, simple to perform, and more rapid than conventional test methods, such as the BACTEC system and the proportion method.
我们之前表明,使用流式细胞术可快速完成对用二醋酸荧光素标记的结核分枝杆菌的药敏试验。然而,安全性是一个主要问题,因为在进行流式细胞术分析之前,分枝杆菌并未被杀死。在本研究中,我们开发了一种生物安全的流式细胞术药敏试验,该试验依赖于在不含药物和含抗分枝杆菌药物的培养基中对活跃生长的结核分枝杆菌进行检测和计数。通过琼脂比例法和流式细胞术方法检测了17株结核分枝杆菌临床分离株对乙胺丁醇、异烟肼和利福平的敏感性。随后,在使用流式细胞仪分析之前,所有流式细胞术药敏试验样品通过暴露于多聚甲醛而被灭活。两种方法的结果一致性为98%。此外,流式细胞术结果在测试开始后72小时即可获得。流式细胞术药敏试验安全、操作简单,且比传统检测方法(如BACTEC系统和比例法)更快。