Alexander L, Veazey R S, Czajak S, DeMaria M, Rosenzweig M, Lackner A A, Desrosiers R C, Sasseville V G
New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772, USA.
AIDS Res Hum Retroviruses. 1999 Jan 1;15(1):11-21. doi: 10.1089/088922299311664.
We engineered recombinant derivatives of simian immunodeficiency virus (SIV) to express enhanced green fluorescent protein (EGFP). Replacement of vpr sequences with EGFP resulted in a genome that did not produce detectable levels of replication-competent virus. Replication-competent virus and bright fluorescence of infected cells were obtained with two other constructs, one in which SIV nef sequences were replaced by EGFP and another in which EGFP was inserted into the SIV nef locus and HIV-1 nef sequences were expressed by downstream placement of an internal ribosomal entry site. These strains were infectious in rhesus monkeys and green fluorescing cells were detected in the tissues of infected monkeys by FACS analysis and by direct microscopic visualization. EGFP sequences were absent from recovered virus by 8 weeks following infection. We conclude that recombinant SIV that is engineered to express EGFP can be used to directly detect productively infected cells and aid in the immunophenotypic characterization of these cells within the first 2 weeks of infection of rhesus monkeys.
我们构建了猿猴免疫缺陷病毒(SIV)的重组衍生物,使其表达增强型绿色荧光蛋白(EGFP)。用EGFP取代vpr序列后得到的基因组无法产生可检测水平的具有复制能力的病毒。通过另外两种构建体获得了具有复制能力的病毒和感染细胞的明亮荧光,一种构建体是将SIV nef序列替换为EGFP,另一种构建体是将EGFP插入SIV nef基因座,并通过内部核糖体进入位点的下游放置来表达HIV-1 nef序列。这些毒株对恒河猴具有感染性,通过流式细胞术分析和直接显微镜观察在感染猴子的组织中检测到了绿色荧光细胞。感染后8周,回收的病毒中不存在EGFP序列。我们得出结论,经设计表达EGFP的重组SIV可用于直接检测高效感染的细胞,并有助于在恒河猴感染的前2周内对这些细胞进行免疫表型特征分析。