Jlizi Asma, Edouard Joanne, Fadhlaoui-Zid Karima, Frigi Sabah, Debré Patrice, Slim Amine, Theodorou Ioannis, El Gaaied Amel Ben Ammar, Carpentier Wassila
Laboratoire de Génétique, Immunologie et Pathologies Humaines, Faculté des Sciences de Tunis, Université Tunis El Manar, Tunis, Tunisie.
Hum Immunol. 2007 Dec;68(12):993-1000. doi: 10.1016/j.humimm.2007.10.003. Epub 2007 Oct 30.
Polymorphisms in some chemokine receptor genes are associated with susceptibility to and progression of human immunodeficiency virus-1 (HIV-1) infection. Most mutations detected in the CC-chemokine receptor 5 (CCR5) gene are specific to different populations. In this study, we focused on polymorphisms of the CCR5 coding region in three healthy populations from Tunisia, corresponding to a cosmopolitan population from Tunis, and two isolated Berber populations. In addition to the CCR5-Delta32 deletion, eleven single nucleotide polymorphisms were detected. Some of these point mutations were associated with the same genotype and even the same haplotype. The (L55Q-C101X), I124, V131F, T143N, A159V, I237, T239A and G301R alleles have not been described previously, whereas the CCR5-Delta32, L55Q, A335V and Y339F variants have already been reported in the literature. The distribution and frequency of these variants were different among the three groups studied, a result in agreement with the mosaic genetic structure of the Tunisian population. To determine whether these alleles affect HIV-1 transmission, we compared allele frequencies between healthy and HIV-1 infected individuals from Tunis. The frequency of the CCR5-Delta32 variant was significantly different between the two groups, leading us to conclude that this mutation might confer protection against HIV infection in Tunisian populations.
某些趋化因子受体基因的多态性与人类免疫缺陷病毒1型(HIV-1)感染的易感性及病情进展相关。在CC趋化因子受体5(CCR5)基因中检测到的大多数突变在不同人群中具有特异性。在本研究中,我们聚焦于来自突尼斯的三个健康人群中CCR5编码区的多态性,这三个群体分别是来自突尼斯的一个国际化人群,以及两个与世隔绝的柏柏尔人群。除了CCR5-Δ32缺失外,还检测到11个单核苷酸多态性。其中一些点突变与相同的基因型甚至相同的单倍型相关。(L55Q-C101X)、I124、V131F、T143N、A159V、I237、T239A和G301R等位基因此前未被描述过,而CCR5-Δ32、L55Q、A335V和Y339F变异体已在文献中报道过。这些变异体在三个研究组中的分布和频率不同,这一结果与突尼斯人群的镶嵌式遗传结构一致。为了确定这些等位基因是否影响HIV-1传播,我们比较了突尼斯健康个体和HIV-1感染个体之间的等位基因频率。两组之间CCR5-Δ32变异体的频率存在显著差异,这使我们得出结论,该突变可能使突尼斯人群对HIV感染具有保护作用。