Rodríguez-Lázaro David, Lloyd Joy, Herrewegh Arnold, Ikonomopoulos John, D'Agostino Martin, Pla Maria, Cook Nigel
Institute of Food and Agricultural Technology, University of Girona, E-17071 Girona, Spain.
FEMS Microbiol Lett. 2004 Aug 1;237(1):119-26. doi: 10.1016/j.femsle.2004.06.024.
A molecular beacon-based real-time NASBA assay for detection and identification of Mycobacterium avium subsp. paratuberculosis has been developed. It targets and amplifies sequences from the dnaA gene which are specific for this bacterium. The assay includes an internal amplification control, to allow identification of inhibited reactions. The assay was tested against 18 isolates of M. avium subsp. paratuberculosis, 17 other mycobacterial strains and 25 non-mycobacterial strains, and was fully selective in that it detected all the targets but none of the non-targets. The lowest number of cells which the assay can detect with 99% probability is 150-200 cells per reaction (as determined using pure culture suspensions). Using centrifugation and nucleic acid extraction as sample treatment, the assay was able to consistently detect 10(3) M. avium subsp. paratuberculosis cells in 20 ml artificially contaminated drinking water. With a simple detergent and enzymatic sample pretreatment before centrifugation and nucleic acid extraction, the assay was able to consistently detect 10(4) M. avium subsp. paratuberculosis cells in 20 ml artificially contaminated semi-skimmed milk. The assay will be a useful addition to the range of diagnostic tools available for the study of M. avium subsp. paratuberculosis.
已开发出一种基于分子信标的实时核酸序列扩增检测法,用于检测和鉴定副结核分枝杆菌。该方法靶向并扩增该细菌特有的dnaA基因序列。该检测法包括一个内部扩增对照,用于识别受抑制的反应。该检测法针对18株副结核分枝杆菌、17株其他分枝杆菌菌株和25株非分枝杆菌菌株进行了测试,具有完全的选择性,即能检测到所有目标菌株,而未检测到任何非目标菌株。该检测法以99%的概率能够检测到的最低细胞数为每个反应150 - 200个细胞(使用纯培养悬浮液测定)。使用离心和核酸提取作为样品处理方法,该检测法能够始终检测出20毫升人工污染饮用水中的10³个副结核分枝杆菌细胞。在离心和核酸提取之前,使用简单的去污剂和酶进行样品预处理,该检测法能够始终检测出20毫升人工污染半脱脂牛奶中的10⁴个副结核分枝杆菌细胞。该检测法将成为可用于副结核分枝杆菌研究的一系列诊断工具中的一项有用补充。