Gupta A, Padh Harish
Department of Cell and Molecular Biology, B.V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Ahmedabad, Gujarat, India.
Int J Immunogenet. 2015 Aug;42(4):270-8. doi: 10.1111/iji.12215. Epub 2015 Jun 21.
HIV-1 infection and progression exhibits interindividual variation. The polymorphism in the chemokine receptors CCR5 and CXCR4, the principal coreceptors for HIV-1 and their ligands like SDF-1 have a profound effect in altering the HIV-1 disease progression rate. A single nucleotide polymorphism designated SDF1-3'UTR-801G-A has been associated with resistance to HIV-1 infection or delayed progression to AIDS. In this study, the SDF1-3'A polymorphism, CCR5∆32 polymorphism and CCR5 promoter polymorphism at positions 58934 G/T, 59029 G/A, 59353 T/C, 59356 C/T, 59402 A/G and 59653 C/T were analysed in Indian population. The polymorphisms in HIV-1 patients and healthy individuals were evaluated by conventional PCR, RFLP-PCR and direct sequencing techniques. The CCR5∆32 mutant allele was found to be almost absent in Indian population. The analysis of the CCR5-59356C/T polymorphism revealed a trend towards an association of the C allele with an increased risk of HIV-1 infection. The frequency of allele CCR5-59356C was higher in HIV-1 patients (100%) as compared to healthy control subjects (89%, P = 0.003). The correlation of SDF1-3'A and CCR5 promoter CCR5-58934G/T, CCR5-59029G/A, CCR5-59353T/C, CCR5-59402 A/G and CCR5-59653C/T polymorphisms and protection to HIV-1 infection and progression to AIDS was found to be nonsignificant. Nine haplotypes with more than 1% frequency were detected but were not significant in their protective role against HIV. Comparative analysis with global populations showed a noteworthy difference in CCR5 and SDF-1 polymorphisms' frequency distribution, indicating the ethnic variability of Indians. Although susceptibility to infections cannot be completely dependent on one or few genetic variants, it is important to remember that SDF-1 and CCR5 variants have been correlated globally with HIV-1 infection and disease progression. In the light of that, higher frequency of SDF-1 variants in the Indian population is noteworthy.
HIV-1感染及病情进展存在个体差异。趋化因子受体CCR5和CXCR4的多态性,作为HIV-1主要的共受体及其配体(如SDF-1),对改变HIV-1疾病进展速率具有深远影响。一种名为SDF1-3'UTR-801G-A的单核苷酸多态性与HIV-1感染抗性或延缓至艾滋病的进展相关。在本研究中,对印度人群中SDF1-3'A多态性、CCR5∆32多态性以及CCR5启动子在58934 G/T、59029 G/A、59353 T/C、59356 C/T、59402 A/G和59653 C/T位点的多态性进行了分析。通过常规PCR、RFLP-PCR和直接测序技术评估了HIV-1患者和健康个体中的多态性。发现CCR5∆32突变等位基因在印度人群中几乎不存在。对CCR5-59356C/T多态性的分析显示,C等位基因与HIV-1感染风险增加之间存在关联趋势。与健康对照受试者(89%,P = 0.003)相比,HIV-1患者中CCR5-59356C等位基因的频率更高(100%)。发现SDF1-3'A与CCR5启动子CCR5-58934G/T、CCR5-59029G/A、CCR5-59353T/C、CCR5-59402 A/G和CCR5-59653C/T多态性以及对HIV-1感染和进展至艾滋病的保护作用之间无显著相关性。检测到9种频率超过1%的单倍型,但它们对HIV的保护作用不显著。与全球人群的比较分析显示,CCR5和SDF-1多态性的频率分布存在显著差异,表明印度人群的种族变异性。尽管对感染易感性不能完全依赖于一个或少数几个基因变异,但重要的是要记住,SDF-1和CCR5变异在全球范围内都与HIV-1感染和疾病进展相关。鉴于此,印度人群中SDF-1变异的较高频率值得关注。