Vener T, Nygren M, Andersson A, Uhlén M, Albert J, Lundeberg J
Department of Biochemistry and Biotechnology, KTH, Royal Institute of Technology, Stockholm, Sweden.
J Clin Microbiol. 1998 Jul;36(7):1864-70. doi: 10.1128/JCM.36.7.1864-1870.1998.
Quantification of human immunodeficiency virus type 1 (HIV-1) RNA in plasma has rapidly become an important tool in basic HIV research and in the clinical care of infected individuals. Here, a quantitative HIV assay based on competitive reverse transcription-PCR with multiple competitors was developed. Four RNA competitors containing identical PCR primer binding sequences as the viral HIV-1 RNA target were constructed. One of the PCR primers was fluorescently labeled, which facilitated discrimination between the viral RNA and competitor amplicons by fragment analysis with conventional automated sequencers. The coamplification of known amounts of the RNA competitors provided the means to establish internal calibration curves for the individual reactions resulting in exclusion of tube-to-tube variations. Calibration curves were created from the peak areas, which were proportional to the starting amount of each competitor. The fluorescence detection format was expanded to provide a dynamic range of more than 5 log units. This quantitative assay allowed for reproducible analysis of samples containing as few as 40 viral copies of HIV-1 RNA per reaction. The within- and between-run coefficients of variation were <24% (range, 10 to 24) and <36% (range, 27 to 36), respectively. The high reproducibility (standard deviation, <0.13 log) of the overall procedure for quantification of HIV-1 RNA in plasma, including sample preparation, amplification, and detection variations, allowed reliable detection of a 0.5-log change in RNA viral load. The assay could be a useful tool for monitoring HIV-1 disease progression and antiviral treatment and can easily be adapted to the quantification of other pathogens.
血浆中人类免疫缺陷病毒1型(HIV-1)RNA的定量分析已迅速成为基础HIV研究以及感染个体临床护理中的一项重要工具。在此,开发了一种基于带有多个竞争物的竞争性逆转录-PCR的HIV定量检测方法。构建了四种RNA竞争物,其含有与病毒HIV-1 RNA靶标相同的PCR引物结合序列。其中一个PCR引物用荧光标记,这便于通过使用传统自动测序仪进行片段分析来区分病毒RNA和竞争物扩增子。已知量的RNA竞争物的共扩增提供了为各个反应建立内部校准曲线的方法,从而排除了管间差异。校准曲线根据峰面积生成,峰面积与每个竞争物的起始量成正比。荧光检测形式得到扩展,以提供超过5个对数单位的动态范围。这种定量检测方法能够对每个反应中低至40个HIV-1 RNA病毒拷贝的样品进行可重复分析。批内和批间变异系数分别<24%(范围为10%至24%)和<36%(范围为27%至36%)。血浆中HIV-1 RNA定量分析的整个过程(包括样品制备、扩增和检测变异)具有高重现性(标准差<0.13对数),能够可靠地检测RNA病毒载量0.5个对数的变化。该检测方法可能是监测HIV-1疾病进展和抗病毒治疗的有用工具,并且可以很容易地适用于其他病原体的定量分析。