Chaix M L, Chappey C, Couillin I, Rozenbaum W, Levy J P, Saragosti S
ICGM, INSERM U363, Hôpital Cochin, Paris, France.
AIDS. 1993 Sep;7(9):1199-204. doi: 10.1097/00002030-199309000-00008.
To carry out, within France, a large-scale molecular epidemiological investigation on the principal neutralizing determinant of HIV-1, located in the third variable region (V3) of the envelope protein. Such investigations are of the utmost importance in the identification and monitoring of the distribution and spread of different viral strains internationally.
Using polymerase chain reaction (PCR), we examined the genetic variation of the V3 region sequences of 28 HIV-infected patients from Paris, France.
Comparison of the Parisian V3 loop sequences with other published data indicates that the range of diversity in France is included within that of a large group that contains sequences from North America, the rest of Europe, Japan, India and Africa. Variability appears to be lower in the V3 loop than in its flanking regions. Five out of the six putative N-linked glycosylation sites show preferential alterations to charged amino acids. We report two motifs at the tip of the loop that have not been described previously.
The structural homogeneity and the wide geographic representation of the major V3 group suggests that a common strategy could be applied to a large proportion of isolates in the development of a broad-spectrum HIV vaccine.
在法国开展一项大规模分子流行病学调查,研究位于包膜蛋白第三可变区(V3)的HIV-1主要中和决定簇。此类调查对于在国际上识别和监测不同病毒株的分布与传播至关重要。
我们采用聚合酶链反应(PCR)检测了来自法国巴黎的28名HIV感染患者V3区序列的基因变异情况。
将巴黎患者的V3环序列与其他已发表数据进行比较,结果表明法国的多样性范围包含在一个大群体的范围内,该群体包含来自北美、欧洲其他地区、日本、印度和非洲的序列。V3环中的变异性似乎低于其侧翼区域。六个推定的N-连接糖基化位点中有五个显示出向带电荷氨基酸的优先改变。我们报告了环末端有两个此前未描述过的基序。
主要V3群体的结构同质性和广泛的地理代表性表明,在开发广谱HIV疫苗时,可对很大一部分分离株应用共同策略。