Sastry Lakshmi, Xu Yi, Duffy Lisa, Koop Sue, Jasti Aparna, Roehl Holger, Jolly Doug, Cornetta Kenneth
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Hum Gene Ther. 2005 Oct;16(10):1227-36. doi: 10.1089/hum.2005.16.1227.
The product-enhanced reverse transcriptase (PERT) assay has been used to detect reverse transcriptase (RT) activity associated with retroviruses. Although the PERT assay has been proposed as a method for detection of replication-competent retrovirus (RCR) and lentivirus (RCL), it has not been rigorously compared with existing methods for RCR and RCL detection. We have assessed the PERT assay for detection of RCL and RCR that may contaminate lentiviral and retroviral vectors and compared it with published methods for RCL (p24gag ELISA/gag PCR) and RCR (S+/L-) detection. Our results suggest that the PERT assay is as sensitive as p24gag ELISA and gag PCR for detection of replication-competent HIV-1 in an RCL detection assay. Comparison of detection of replication-competent retroviruses, GALV and RD114, by extended S+/L- and PERT assays indicates that both assays can detect 1 IU of each virus. Our findings suggest that the PERT assay can be used for RCL and RCR testing of a variety of retroviral vectors regardless of the structure, sequence, and envelope of the vectors.
产品增强型逆转录酶(PERT)检测法已用于检测与逆转录病毒相关的逆转录酶(RT)活性。尽管PERT检测法已被提议作为检测复制型逆转录病毒(RCR)和慢病毒(RCL)的一种方法,但尚未与现有的RCR和RCL检测方法进行严格比较。我们评估了PERT检测法用于检测可能污染慢病毒和逆转录病毒载体的RCL和RCR,并将其与已发表的RCL(p24gag ELISA/gag PCR)和RCR(S+/L-)检测方法进行比较。我们的结果表明,在RCL检测试验中,PERT检测法对于检测具有复制能力的HIV-1与p24gag ELISA和gag PCR一样敏感。通过扩展的S+/L-和PERT检测法对具有复制能力的逆转录病毒GALV和RD114的检测比较表明,两种检测法均可检测到每种病毒1个国际单位。我们的研究结果表明,无论载体的结构、序列和包膜如何,PERT检测法均可用于多种逆转录病毒载体的RCL和RCR检测。