摘要
作者合成两对引物,建立结核杆菌DNA多重PcR法,用以检测分枝杆菌标准菌株,仅人型和牛型结核杆菌呈阳性,灵敏度≥7cfu结核杆菌呈阳性。40例肺结核患者痰,经多重PCR法检测27例呈阳性,而采用Bactcc460TB系统快速培养法培养仅19例阳性;多重PCR法栓出率较一对引物PCR法高15%~17.5%,具有较好的敏感性和林异性。
wo pairs of primers were synthesized and a multiplex PCR method in detecting M. tuberculosisDNA was developed. The standard strain of Mycobacterium was detected by the multi-PCR. The resultshowed that only M. tuberculosis and M. Bovis were positive. The detective sensitivity of multi-PCRwas≥7 CFU for M. tuberculosis,The sputa of 40 patients with pulmonary tuberculosis were examinedby this method and by the bactec 460 TB system. The positive results in mulit-PCR were 27/40 and inbactec method 19/40( P <0.05).The detection rate of multi-PCR was 15%~17.5%higher than thatwith one pair of primers( P<0. 025).
出处
《中国医科大学学报》
CAS
CSCD
1996年第2期186-188,共3页
Journal of China Medical University
基金
辽宁省科委