Müller Jens, Eis-Hübinger Anna Maria, Däumer Martin, Kaiser Rolf, Rox Jutta Maria, Gürtler Lutz, Hanfland Peter, Pötzsch Bernd
Institute of Experimental Haematology and Transfusion Medicine, Rheinische Friedrich-Wilhelms-University, Sigmund-Freud-Strasse 25, 53105 Bonn, Germany.
J Virol Methods. 2007 Jun;142(1-2):127-35. doi: 10.1016/j.jviromet.2007.01.013. Epub 2007 Feb 26.
Given the worldwide increasing spread of HIV-1 genetic variants, it is mandatory that assays used for nucleic acid testing for HIV-1 detect all existing groups and subtypes of HIV-1. In this report the development and evaluation of a quantitative real-time HIV-1 RT-PCR assay that targets a conserved region within the pol integrase domain is described. As an internal control reaction, endogenous glyceraldehyde-3-phosphate-dehydrogenase transcripts were detected in a multiplex configuration. The detection limit (95% cut-off value) was determined by probit analysis and calculated as 281 IU/ml of HIV-1 RNA. Within-run and between-run coefficients of variation were below 15 and 27%, respectively, indicating high reproducibility. The described assay detected all tested HIV-1 isolates representing groups M, O and N. Within group M, quantitative test results correlated well with viral loads as determined by the automated Abbott RealTime HIV-1 assay. Based on the testing of 1206 confirmed HIV-1 RNA negative blood donor samples, assay specificity was found to be 100%. The rate of inhibition was 0.37%. The described HIV-1 real-time RT-PCR was validated according to regulatory guidelines and is applicable to the screening of blood donors as well as the determination of HIV-1 viral load.
鉴于HIV-1基因变异体在全球范围内的传播日益增加,用于HIV-1核酸检测的检测方法必须能够检测到HIV-1的所有现有组和亚型。在本报告中,描述了一种针对pol整合酶结构域内保守区域的定量实时HIV-1 RT-PCR检测方法的开发和评估。作为内部对照反应,在内参配置中检测内源性甘油醛-3-磷酸脱氢酶转录本。检测限(95%临界值)通过概率分析确定,计算为281 IU/ml的HIV-1 RNA。批内和批间变异系数分别低于15%和27%,表明重现性高。所述检测方法检测了代表M、O和N组的所有测试HIV-1分离株。在M组内,定量检测结果与通过雅培实时HIV-1自动化检测法测定的病毒载量相关性良好。基于对1206份经确认的HIV-1 RNA阴性献血者样本的检测,发现检测方法的特异性为100%。抑制率为0.37%。所述HIV-1实时RT-PCR根据监管指南进行了验证,适用于献血者筛查以及HIV-1病毒载量的测定。