Sellner L N, Coelen R J, Mackenzie J S
Department of Microbiology, QEII Medical Centre, University of Western Australia, Nedlands, Perth.
J Virol Methods. 1994 Aug;49(1):47-58. doi: 10.1016/0166-0934(94)90054-x.
A sensitive nested RT-PCR that can be carried out in a single tube is described. The sensitivity of this system was determined, and compared to that of a single round of PCR, and a single round of PCR followed by hybridisation with a radiolabelled oligonucleotide probe. We found that with the one-tube nested RT-PCR we were able to detect 0.1 pfu/ml of Ross River virus. The nested RT-PCR was 100-times more sensitive than a single round of RT-PCR followed by hybridisation, and 10,000-times more sensitive than a single round of RT-PCR alone. This system provides a sensitive detection of Ross River virus, and can be adapted for detection of RNA from any source. The test material is added to a single tube at the outset, and by subsequent addition of two sets of reagents, the entire nested RT-PCR can be carried out in the same tube. This system has maximum sensitivity, minimises risk of contamination, and is amenable to automation.
本文描述了一种可在单管中进行的灵敏巢式逆转录聚合酶链反应(RT-PCR)。测定了该系统的灵敏度,并与一轮PCR以及一轮PCR后用放射性标记的寡核苷酸探针杂交的灵敏度进行了比较。我们发现,使用单管巢式RT-PCR能够检测到0.1个空斑形成单位/毫升的罗斯河病毒。巢式RT-PCR的灵敏度比一轮RT-PCR后杂交高100倍,比单独一轮RT-PCR高10000倍。该系统可灵敏检测罗斯河病毒,并且可适用于检测任何来源的RNA。测试材料在一开始就添加到单管中,通过随后添加两组试剂,整个巢式RT-PCR可在同一管中进行。该系统具有最高的灵敏度,将污染风险降至最低,并且适合自动化操作。