Arnold B A, Hepler R W, Keller P M
Department of Virus and Cell Biology, Merck Research Laboratories, West Point, PA 19486-0004, USA.
Biotechniques. 1998 Jul;25(1):98-106. doi: 10.2144/98251st06.
Recently developed PCR-based reverse transcriptase (RT) assays are useful in the detection of retroviruses since they are approximately a millionfold more sensitive than conventional RT assays. However, these assays are both labor- and time-intensive. The previously described product-enhanced reverse transcriptase (PERT) assay involves a two-step RT-PCR followed by detection and quantitation of PCR products by either Southern blot or enzyme-linked immunosorbent assay (ELISA). We have modified the PERT assay to be a one-step, fluorescent probe, PCR-based RT assay that can be completed from sample dilution to final quantitative assay results in approximately 5 h without loss of assay sensitivity or specificity. The assay has a dynamic range of 6 logs, and therefore, extensive sample dilution is not necessary for quantitation. This newly enhanced fluorescent PERT assay can play an important role in the high-throughput detection of retroviral infection and characterization of RT activity.
最近开发的基于聚合酶链反应(PCR)的逆转录酶(RT)检测方法在逆转录病毒检测中很有用,因为它们的灵敏度比传统RT检测方法高约一百万倍。然而,这些检测方法既耗费人力又耗时。先前描述的产物增强逆转录酶(PERT)检测方法包括两步RT-PCR,随后通过Southern印迹或酶联免疫吸附测定(ELISA)检测和定量PCR产物。我们已将PERT检测方法改进为一步法荧光探针PCR-based RT检测方法,该方法可在约5小时内从样品稀释完成至最终定量检测结果,而不会损失检测灵敏度或特异性。该检测方法的动态范围为6个对数,因此,定量时无需进行大量样品稀释。这种新增强的荧光PERT检测方法可在逆转录病毒感染的高通量检测和RT活性表征中发挥重要作用。