Rhodes Terence D, Nikolaitchik Olga, Chen Jianbo, Powell Douglas, Hu Wei-Shau
HIV Drug Resistance Program, NCI-Frederick, PO Box B, Building 535, Room 336, Frederick, MD 21702, USA.
J Virol. 2005 Feb;79(3):1666-77. doi: 10.1128/JVI.79.3.1666-1677.2005.
Recombination is a major mechanism that generates variation in populations of human immunodeficiency virus type 1 (HIV-1). Mutations that confer replication advantages, such as drug resistance, often cluster within regions of the HIV-1 genome. To explore how efficiently HIV-1 can assort markers separated by short distances, we developed a flow cytometry-based system to study recombination. Two HIV-1-based vectors were generated, one encoding the mouse heat-stable antigen gene and green fluorescent protein gene (GFP), and the other encoding the mouse Thy-1 gene and GFP. We generated derivatives of both vectors that contained nonfunctional GFP inactivated by different mutations. Recombination in the region between the two inactivating mutations during reverse transcription could yield a functional GFP. With this system, we determined that the recombination rates of markers separated by 588, 300, 288, and 103 bp in one round of viral replication are 56, 38, 31, and 12%, respectively, of the theoretical maximum measurable recombination rate. Statistical analyses revealed that at these intervals, recombination rates and marker distances have a near-linear relationship that is part of an overall quadratic fit. Additionally, we examined the segregation of three markers within 600 bp and concluded that HIV-1 crossover events do not exhibit high negative interference. We also examined the effects of target cells and viral accessory proteins on recombination rate. Similar recombination rates were observed when human primary CD4(+) T cells and a human T-cell line were used as target cells. We also found equivalent recombination rates in the presence and absence of accessory genes vif, vpr, vpu, and nef. These results illustrate the power of recombination in generating viral population variation and predict the rapid assortment of mutations in the HIV-1 genome in infected individuals.
重组是在1型人类免疫缺陷病毒(HIV-1)群体中产生变异的主要机制。赋予复制优势(如耐药性)的突变通常聚集在HIV-1基因组区域内。为了探究HIV-1能多高效地对近距离分隔的标记进行分类,我们开发了一种基于流式细胞术的系统来研究重组。构建了两种基于HIV-1的载体,一种编码小鼠热稳定抗原基因和绿色荧光蛋白基因(GFP),另一种编码小鼠Thy-1基因和GFP。我们构建了这两种载体的衍生物,它们含有因不同突变而失活的无功能GFP。逆转录过程中两个失活突变之间区域的重组可产生功能性GFP。利用该系统,我们确定在一轮病毒复制中,间隔588、300、288和103 bp的标记的重组率分别为理论最大可测量重组率的56%、38%、31%和12%。统计分析表明,在这些间隔下,重组率与标记距离具有近线性关系,这是整体二次拟合的一部分。此外,我们研究了600 bp内三个标记的分离情况,得出HIV-1交叉事件不表现出高负干扰的结论。我们还研究了靶细胞和病毒辅助蛋白对重组率的影响。当使用人原代CD4(+) T细胞和人T细胞系作为靶细胞时,观察到相似的重组率。我们还发现在存在和不存在辅助基因vif、vpr、vpu和nef的情况下重组率相当。这些结果说明了重组在产生病毒群体变异方面的作用,并预测了感染个体中HIV-1基因组中突变的快速分类。