Moore D F, Curry J I
Public Health Laboratory, Orange County Health Care Agency, Santa Ana, California 92706, USA.
J Clin Microbiol. 1995 Oct;33(10):2686-91. doi: 10.1128/jcm.33.10.2686-2691.1995.
Sputum specimens received for the diagnosis of tuberculosis or other mycobacterial infections were tested by a PCR-based assay and culture techniques. Results of the PCR assay (Amplicor Mycobacterium tuberculosis Test) were compared with results of standard culture techniques with cultures held for 6 weeks. One thousand nine specimens were included: 301 retrospective specimens (frozen at -70 degrees C and later tested by PCR) and 708 prospective specimens (tested within 1 day of processing). One hundred sixty-two (16%) of the specimens were culture positive for M. tuberculosis; 83 (51%) of these were also fluorochrome stain positive. The sensitivity and specificity of the Amplicor PCR compared with those of culture were 83% (134 of 162 specimens) and 97% (800 of 827 specimens), respectively. The sensitivity for fluorochrome stain-positive specimens was 99%, and that for fluorochrome stain-negative specimens was 66%. The great majority of the 28 PCR-negative, culture-positive specimens were low positives; 27 were smear negative and 19 contained < 100 CFU of M. tuberculosis per ml. The 27 PCR-positive, culture-negative specimens included 24 that were positive by repeat testing by alternate primer PCR and were from patients with tuberculosis on antimicrobial therapy. With these considered culture misses, the final sensitivities of PCR and culture were 85, and 87%, respectively, while the specificities were 99.6 and 100%, respectively. After normal laboratory processing of sputum specimens, the Amplicor PCR assay can be completed in 8 h. Thus, it is possible to have results available within 10 h of specimen submission.
接收用于诊断结核病或其他分枝杆菌感染的痰标本,采用基于聚合酶链反应(PCR)的检测方法和培养技术进行检测。将PCR检测结果(Amplicor结核分枝杆菌检测)与标准培养技术的结果进行比较,培养物保存6周。共纳入1900份标本:301份回顾性标本(保存在-70℃并随后进行PCR检测)和708份前瞻性标本(在处理后1天内检测)。162份(16%)标本结核分枝杆菌培养阳性;其中83份(51%)荧光染色也呈阳性。与培养相比,Amplicor PCR的敏感性和特异性分别为83%(162份标本中的134份)和97%(827份标本中的800份)。荧光染色阳性标本的敏感性为99%,荧光染色阴性标本的敏感性为66%。28份PCR阴性、培养阳性的标本中,绝大多数为低阳性;27份涂片阴性,19份每毫升含结核分枝杆菌<100菌落形成单位(CFU)。27份PCR阳性、培养阴性的标本中,24份经交替引物PCR重复检测呈阳性,且来自接受抗菌治疗的结核病患者。考虑到这些培养漏检情况,PCR和培养的最终敏感性分别为85%和87%,而特异性分别为99.6%和100%。经过痰标本的常规实验室处理后,Amplicor PCR检测可在8小时内完成。因此,在标本提交后10小时内有可能获得结果。