Badak F Z, Goksel S, Sertoz R, Nafile B, Ermertcan S, Cavusoglu C, Bilgic A
Department of Clinical Microbiology, Ege University Medical School, Izmir, Turkey.
J Clin Microbiol. 1999 May;37(5):1602-5. doi: 10.1128/JCM.37.5.1602-1605.1999.
The feasibility of using nucleic acid probes directly from positive MB/BacT broth to identify mycobacteria was determined in this study. A total number of 2,727 specimens were cultured into the MB/BacT (Organon Teknika) automated system and on conventional Loweinstein-Jensen (LJ) slants. The Gen-Probe AccuProbe culture identification tests (DNA probes) were used on samples from bottles which were identified as positive for mycobacteria by MB/BacT. Samples of positive MB/BacT broth (0.1 ml) were used directly in the broth culture method for the DNA probes as published by Gen-Probe. Centrifugation of the contents of the bottle was not done prior to probe testing. The number of mycobacteria detected by MB/BacT and LJ was 253 (221 isolates of M. tuberculosis and 32 isolates of mycobacteria other than M. tuberculosis [MOTT]). A total of 96.4% (213 of 221) of the bottles growing M. tuberculosis produced a positive direct DNA probe result for M. tuberculosis complex. One hundred percent (16 of 16) of the bottles growing M. gordonae produced a positive direct DNA probe result for M. gordonae. A total of 3.6% (8 of 221) of the bottles growing M. tuberculosis did not yield a positive direct DNA probe result for M. tuberculosis complex. The testing of subcultures made onto solid media from the positive bottles by AccuProbe identified six of these eight M. tuberculosis isolates. Two (0.9%) M. tuberculosis isolates gave a negative result for the M. tuberculosis probe test applied on the MB/BacT broth and its subculture. The rest of the positive MB/BacT bottles growing MOTT (16 of 32) were negative for M. gordonae, M. avium, M. intracellulare, and M. kansasii probes. The sensitivity and specificity of AccuProbe for the identification of M. tuberculosis and M. gordonae directly from MB/BacT broth were 96.4 and 100% for M. tuberculosis and 100 and 100% for M. gordonae, respectively. The direct testing of positive MB/BacT broth by AccuProbe, without prior centrifugation, allows for the accurate and rapid identification of M. tuberculosis and M. gordonae.
本研究确定了直接使用来自阳性MB/BacT肉汤的核酸探针鉴定分枝杆菌的可行性。总共2727份标本接种于MB/BacT(奥加农泰克尼卡公司)自动化系统和传统的罗-琴(LJ)斜面培养基上。对MB/BacT鉴定为分枝杆菌阳性的瓶内样本进行Gen-Probe AccuProbe培养物鉴定试验(DNA探针)。按照Gen-Probe公布的方法,将阳性MB/BacT肉汤样本(0.1 ml)直接用于DNA探针的肉汤培养法。在进行探针检测前未对瓶内内容物进行离心。MB/BacT和LJ检测到的分枝杆菌数量为253株(221株结核分枝杆菌和32株非结核分枝杆菌[MOTT])。培养结核分枝杆菌的瓶中,共有96.4%(221株中的213株)产生结核分枝杆菌复合群的阳性直接DNA探针结果。培养戈登分枝杆菌的瓶中,100%(16株中的16株)产生戈登分枝杆菌的阳性直接DNA探针结果。培养结核分枝杆菌的瓶中,共有3.6%(221株中的8株)未产生结核分枝杆菌复合群的阳性直接DNA探针结果。通过AccuProbe对阳性瓶接种到固体培养基上的亚培养物进行检测,鉴定出这8株结核分枝杆菌中的6株。两株(0.