Buck G E, O'Hara L C, Summersgill J T
Clinical Laboratory, Alliant Health System, Louisville, Kentucky 40232.
J Clin Microbiol. 1992 May;30(5):1331-4. doi: 10.1128/jcm.30.5.1331-1334.1992.
Several simplified methods for treating mycobacteria to release DNA for amplification by the polymerase chain reaction (PCR) were investigated. The most effective of the methods was sonication. Samples were placed in screw-capped microcentrifuge tubes that were then placed in a plastic rack. The rack was floated in a dish of water next to the ultrasonic probe so that the ultrasonic energy was transmitted through the walls of the tubes. This allowed multiple samples to be processed safely and effectively. Forty-three clinical samples were processed by this procedure, and the crude preparations were analyzed for Mycobacterium tuberculosis by PCR. Twenty-six of these specimens contained M. tuberculosis, and 17 either had no growth or contained other species of mycobacteria. Twenty-four of the 26 (92%) positive specimens were correctly identified, and all of the negative specimens were correctly identified. This sonication procedure appears promising as a rapid, simple means of treating clinical specimens containing mycobacteria for PCR analysis.
研究了几种用于处理分枝杆菌以释放DNA进行聚合酶链反应(PCR)扩增的简化方法。其中最有效的方法是超声处理。将样品置于带螺旋盖的微量离心管中,然后将这些管子放入塑料架中。该架子漂浮在靠近超声探头的一盘水中,以便超声能量通过管壁传递。这使得多个样品能够安全有效地进行处理。通过该程序处理了43份临床样品,并通过PCR分析粗制品中的结核分枝杆菌。这些标本中有26份含有结核分枝杆菌,17份没有生长或含有其他分枝杆菌种类。26份阳性标本中有24份(92%)被正确鉴定,所有阴性标本均被正确鉴定。这种超声处理程序作为一种快速、简单的处理含分枝杆菌临床标本进行PCR分析的方法,似乎很有前景。