Rocancourt D, Bonnerot C, Jouin H, Emerman M, Nicolas J F
Unité de Biologie moléculaire du Développement, Unité Associée 1148 du Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France.
J Virol. 1990 Jun;64(6):2660-8. doi: 10.1128/JVI.64.6.2660-2668.1990.
A quantitative bioassay for human immunodeficiency viruses has been developed on the basis of the ability of the tat gene to transactivate the expression of an integrated beta-galactosidase gene in a HeLa-CD4+ cell line. Infection by a single virion of HIV-1 or HIV-2 corresponds to a unique blue syncytium or a cell cluster detected after fixation and addition of 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside (a beta-galactosidase substrate). The number of infected lymphoid cells in a culture (stimulated human peripheral blood lymphocytes and cell lines) can also be quantified by cell-to-cell transmission of HIV into the HeLa-CD4(+)-beta-galactosidase monolayer. Infections by simian immunodeficiency viruses are similarly detected. This assay has been used to determine the dose response of drugs, the half-life of HIV at 37 degrees C, and the appearance of infectious particles after virus infection.
基于tat基因激活HeLa - CD4 +细胞系中整合的β - 半乳糖苷酶基因表达的能力,已开发出一种用于人类免疫缺陷病毒的定量生物测定法。单个HIV - 1或HIV - 2病毒体感染对应于固定后并添加5 - 溴 - 4 - 氯 - 3 - 吲哚基 - β - D - 吡喃半乳糖苷(一种β - 半乳糖苷酶底物)后检测到的独特蓝色多核巨细胞或细胞簇。培养物(刺激的人外周血淋巴细胞和细胞系)中受感染淋巴细胞的数量也可以通过HIV在HeLa - CD4(+) - β - 半乳糖苷酶单层中的细胞间传播来定量。猿猴免疫缺陷病毒感染也能以类似方式检测到。该测定法已用于确定药物的剂量反应、HIV在37摄氏度下的半衰期以及病毒感染后感染性颗粒的出现情况。