Teglbjaerg L L, Nielsen C, Hansen J E
Department of Infectious Diseases, Hvidovre Hospital, Denmark.
Mol Cell Probes. 1992 Jun;6(3):175-80. doi: 10.1016/0890-8508(92)90014-o.
This report describes the use of the polymerase chain reaction (PCR) for the non-radioactive detection of HIV-1 proviral genomic sequences in HIV-1 infected cells. We have developed a sensitive assay, using three different sets of nested primers and our results show that this method is superior to standard PCR for the detection of HIV-1 DNA. The assay described features the use of a simple and inexpensive sample preparation technique and a non-radioactive hybridization procedure for confirmation of results. To test the suitability of the assay for clinical purposes, we tested cell samples from 76 anti-HIV-1 positive patients. All were positive for at least one primer set: 88% were positive for all three sets of primers; 9% were positive for two sets of primers and 3% were positive for only one set of primers. It provides a useful approach to the study of HIV-1 infection in patient samples where genomic copies often are present at such low numbers that they are otherwise undetectable.
本报告描述了使用聚合酶链反应(PCR)对HIV-1感染细胞中的HIV-1前病毒基因组序列进行非放射性检测。我们开发了一种灵敏的检测方法,使用了三组不同的巢式引物,结果表明该方法在检测HIV-1 DNA方面优于标准PCR。所描述的检测方法具有使用简单且廉价的样品制备技术以及用于结果确认的非放射性杂交程序的特点。为了测试该检测方法用于临床目的的适用性,我们检测了76例抗HIV-1阳性患者的细胞样本。所有样本至少对一组引物呈阳性:88%对所有三组引物呈阳性;9%对两组引物呈阳性,3%仅对一组引物呈阳性。它为研究患者样本中的HIV-1感染提供了一种有用的方法,在这些样本中基因组拷贝数通常很低,否则难以检测到。