Laboratory of Molecular Virology, Faculty of Health Science, University of Brasilia, Brasilia, DF, Brazil.
Protein J. 2012 Feb;31(2):184-93. doi: 10.1007/s10930-011-9389-y.
One of the most studied topics about AIDS disease is the presence of different progression levels in patients infected by HIV. Several studies have shown that this progression is directly associated with host genetics, although viral factors are also known to play a role. Here we explore the contribution of Vpu protein in the evolution of viral population. The sequence variation of Vpu was analyzed during HIV infection in peripheral blood monocyte cells of 12 patients in different clinical stages of HIV-1 infection early and late stages of infections, separated by at least 4 years. The clustering analysis of Vpu sequences showed higher diversity of early alleles, non-random distribution of sequences, and viral evolution strains selection. Forty-two amino acid modifications were found in the multiple alignments of the 57 different alleles found for early stage were 23 modifications were found in the late stage dataset. Interestingly fourteen alteration of early stage were located in conserved site related with Vpu functions alterations while these alterations appear with less frequency in the late stage of infection. Moreover, late stage alleles tend to be similar with the Vpu wild type sequence, suggesting viral selection toward populations harboring more efficient variants during the course of infection. This would contribute to higher infectivity and viral replication actually observed at the aggressive late stages of infection. These data, in conjunction with in vitro experiments, will be important to elucidation of the physiological relevance of Vpu protein in the pathogenic mechanisms of AIDS.
艾滋病研究中最热门的课题之一是 HIV 感染者体内不同的疾病进展水平。有多项研究表明,这种进展与宿主遗传学直接相关,尽管病毒因素也被认为起一定作用。在这里,我们研究了 Vpu 蛋白在病毒种群进化中的作用。对 12 名处于 HIV-1 感染早、晚期不同临床阶段的患者外周血单核细胞中 Vpu 的序列变异进行了分析,两次采血时间至少相隔 4 年。Vpu 序列聚类分析显示早期等位基因多样性较高,序列非随机分布,病毒进化株选择。在对 57 个不同早期等位基因的多重比对中发现了 42 个氨基酸修饰,在晚期数据集发现了 23 个修饰。有趣的是,早期阶段的 14 个改变位于与 Vpu 功能改变相关的保守位点,而这些改变在感染晚期出现的频率较低。此外,晚期等位基因往往与 Vpu 野生型序列相似,这表明在感染过程中病毒选择了更有效的变体种群。这将有助于解释在感染晚期观察到的高传染性和病毒复制现象。这些数据与体外实验相结合,将有助于阐明 Vpu 蛋白在艾滋病发病机制中的生理相关性。