Abe C
Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo.
Kekkaku. 1994 Aug;69(8):527-33.
Two systems, radiometric BACTEC and biphasic MB-Check, based on liquid media proved to be significantly better than the egg-based solid media for the isolation of mycobacteria from clinical specimens. The difference in the rates of isolation of mycobacteria between two groups of media was more remarkable with smear-negative specimens. The time to the detection of the Mycobacterium tuberculosis complex with MB- Check was shorter than that with the 3% Ogawa egg method but longer than that with BACTEC. The polymerase chain reaction (PCR) using oligonucleotides based on the repetitive sequence (IS986) of M. tuberculosis as a primer and the Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test (MTD), which combines an M. tuberculosis rRNA amplification method with the hybridization protection assay format, were evaluated for detection of M. tuberculosis in clinical samples. Although the sensitivities of the PCR and MTD appeared to be similar to that of culture with the MB-Check system, the two methods based on nucleic acid amplification should be very useful for rapid detection of M. tuberculosis infections without the long time required for culture of M. tuberculosis. Epidemiological studies with techniques which allow differentiation of strains within M. tuberculosis groups are important for limiting the dissemination of the disease. We analyzed six groups of small outbreaks of M. tuberculosis infections by restriction fragment length polymorphism (RFLP) analysis. Five showed identical fingerprints within each group, but one which as also suspected to have a common source of infection showed different banding patterns, emphasizing that RFLP analysis using IS986 as a probe is useful in epidemiological studies of tuberculosis.(ABSTRACT TRUNCATED AT 250 WORDS)
基于液体培养基的两种系统,即放射性BACTEC系统和双相MB-Check系统,在从临床标本中分离分枝杆菌方面,被证明明显优于基于鸡蛋的固体培养基。两组培养基在分枝杆菌分离率上的差异,在涂片阴性标本中更为显著。使用MB-Check检测结核分枝杆菌复合群的时间,比使用3%小川鸡蛋培养基法要短,但比使用BACTEC法要长。对以结核分枝杆菌重复序列(IS986)为引物的寡核苷酸聚合酶链反应(PCR)以及将结核分枝杆菌rRNA扩增方法与杂交保护分析形式相结合的Gen-Probe结核分枝杆菌直接扩增检测法(MTD),进行了临床样本中结核分枝杆菌检测的评估。尽管PCR和MTD的灵敏度似乎与MB-Check系统培养法相似,但这两种基于核酸扩增的方法对于快速检测结核分枝杆菌感染非常有用,无需像培养结核分枝杆菌那样花费很长时间。采用能够区分结核分枝杆菌组内菌株的技术进行流行病学研究,对于限制疾病传播很重要。我们通过限制性片段长度多态性(RFLP)分析,对六组结核分枝杆菌感染的小规模暴发进行了分析。五组在每组内显示出相同的指纹图谱,但另一组也怀疑有共同感染源的却显示出不同的条带模式,这强调了以IS986为探针的RFLP分析在结核病流行病学研究中的作用。(摘要截短于250词)