Felber B K, Pavlakis G N
National Cancer Institute, Frederick Cancer Research Facility, Bionetics Research, Inc., MD 21701.
Science. 1988 Jan 8;239(4836):184-7. doi: 10.1126/science.3422113.
A bioassay that is based on trans-activation has been developed for the detection and quantitation of the human immunodeficiency virus type 1 (HIV-1). Indicator cell lines were constructed that contain the HIV-1 long terminal repeat ligated to the chloramphenicol acetyltransferase (CAT) gene. Infection of these cells by HIV activates the expression of CAT protein. Isolates of HIV-1 with divergent nucleotide sequences activated the indicator cell lines to a similar extent, approximately 500- to 1000-fold. Human T cell lymphotropic viruses types 1 and 2, equine infectious anemia virus, and herpes simplex virus 1 did not activate the indicator cell lines. Isolates of simian immunodeficiency virus and human T cell lymphotropic virus type 4 activated these cells to a much lesser extent, which suggests that these viruses contain similar, but distinct, trans-activators. This assay can be used for the detection, quantitation, and typing of HIV and for studying the effect of drugs on the replication of HIV in different cellular backgrounds.
已开发出一种基于反式激活的生物测定法,用于检测和定量1型人类免疫缺陷病毒(HIV-1)。构建了指示细胞系,其包含与氯霉素乙酰转移酶(CAT)基因连接的HIV-1长末端重复序列。HIV感染这些细胞会激活CAT蛋白的表达。具有不同核苷酸序列的HIV-1分离株激活指示细胞系的程度相似,约为500至1000倍。1型和2型人类嗜T细胞病毒、马传染性贫血病毒和单纯疱疹病毒1均未激活指示细胞系。猿猴免疫缺陷病毒和4型人类嗜T细胞病毒的分离株激活这些细胞的程度要小得多,这表明这些病毒含有相似但不同的反式激活因子。该测定法可用于HIV的检测、定量和分型,以及研究药物在不同细胞背景下对HIV复制的影响。