Kam K M, Yip C W, Chan M Y, Mok C Y, Wong W S
Yung Fung Shee Memorial Center, Department of Health, Hong Kong, China.
Diagn Microbiol Infect Dis. 1999 Jan;33(1):13-8. doi: 10.1016/s0732-8893(98)00136-9.
To explore a simple, rapid, and inexpensive way to identify Mycobacterium tuberculosis complex culture, dot blot hybridization using IS6110 as the marker was performed against 2788 known clinical isolates of mycobacteria including M. tuberculosis (n = 721), M. kansasii (177), M. marinum (10), M. avium complex (700), M. terrae complex (203), M. fortuitum (476), M. chelonae (439), and other nonpigmented Runyon's Group IV mycobacteria (62). We found that the sensitivity and specificity of the test were 94.3% and 100%, respectively. When this method was evaluated in a laboratory blind study of 1253 initially unknown clinical isolates, its sensitivity and specificity were 91.2% and 100%, respectively. Because this identification test is technically simple, rapid, and can be done in batches, together with its high sensitivity and specificity, it is a cost-effective method for routine identification of M. tuberculosis complex in laboratories of areas with a high incidence of tuberculosis.
为探索一种简单、快速且经济的方法来鉴定结核分枝杆菌复合群培养物,以IS6110为标记进行斑点杂交,检测了2788株已知的分枝杆菌临床分离株,包括结核分枝杆菌(n = 721)、堪萨斯分枝杆菌(177株)、海分枝杆菌(10株)、鸟分枝杆菌复合群(700株)、土分枝杆菌复合群(203株)、偶然分枝杆菌(476株)、龟分枝杆菌(439株)以及其他非色素沉着的Runyon IV群分枝杆菌(62株)。我们发现该检测方法的敏感性和特异性分别为94.3%和100%。在对1253株最初未知的临床分离株进行的实验室盲法研究中评估该方法时,其敏感性和特异性分别为91.2%和100%。由于这种鉴定试验技术简单、快速且可批量进行,同时具有高敏感性和特异性,因此对于结核病高发地区的实验室来说,是一种用于常规鉴定结核分枝杆菌复合群的经济有效的方法。