Badak F Z, Kiska D L, O'Connell M, Nycz C M, Hartley C, Setterquist S, Hopfer R L
Becton Dickinson Research Center, Research Triangle Park, North Carolina, USA.
J Clin Microbiol. 1997 May;35(5):1239-43. doi: 10.1128/jcm.35.5.1239-1243.1997.
Multiplex strand displacement amplification (mSDA) is capable of amplifying three distinct DNA sequences simultaneously. These include sequences present in most genera of mycobacteria, a sequence specific for Mycobacterium tuberculosis, and an internal control. mSDA was used to detect the presence of these target sequences in 154 (72 positive, 76 negative, and 6 failed) clinical specimens cultured in the mycobacterial growth indicator tube (MGIT) system. A wide variety of specimen types were processed and cultured. Once these cultures were deemed positive by MGIT fluorescence or were deemed negative after 8 weeks of incubation, MGIT culture aliquots were processed for mSDA analyses. A chemiluminescent microwell assay was used to detect the amplified products. The procedure was relatively simple and took less than 6 h to complete. The sensitivity of mSDA for detecting acid-fast bacilli was 96.4% compared to that of MGIT culture. Sensitivity and specificity were 97.2 and 96.1%, respectively, when all clinical criteria were considered. mSDA was shown to be a rapid and effective method for confirming the presence of M. tuberculosis and other mycobacteria in positive MGIT cultures.
多重链置换扩增(mSDA)能够同时扩增三个不同的DNA序列。这些序列包括大多数分枝杆菌属中存在的序列、结核分枝杆菌特异的序列以及一个内部对照。mSDA用于检测在分枝杆菌生长指示管(MGIT)系统中培养的154份临床标本(72份阳性、76份阴性和6份检测失败)中这些靶序列的存在。处理和培养了多种标本类型。一旦这些培养物经MGIT荧光判定为阳性或在培养8周后判定为阴性,就对MGIT培养物的等分试样进行mSDA分析。采用化学发光微孔测定法检测扩增产物。该程序相对简单,完成时间不到6小时。与MGIT培养相比,mSDA检测抗酸杆菌的灵敏度为96.4%。当考虑所有临床标准时,灵敏度和特异性分别为97.2%和96.1%。mSDA被证明是一种快速有效的方法,可用于确认阳性MGIT培养物中结核分枝杆菌和其他分枝杆菌的存在。