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HIV/AIDS保护性基因SDF1、CCR5和CCR2变体在克里特岛人群中的分布情况。

Distribution of HIV/AIDS protective SDF1, CCR5 and CCR2 gene variants within Cretan population.

作者信息

Apostolakis S, Baritaki S, Krambovitis E, Spandidos D A

机构信息

Laboratory of Virology, Faculty of Medicine, University of Crete, Heraklion 71110, Crete, Greece.

出版信息

J Clin Virol. 2005 Dec;34(4):310-4. doi: 10.1016/j.jcv.2005.01.010.

Abstract

An interesting finding in the epidemiology of human immunodeficiency virus (HIV) infection is that certain mutations in genes coding for chemokine receptors and their ligands may confer resistance to HIV-1 infection and/or AIDS progression. The mutations most frequently studied are the CCR5-delta32, CCR2-64I and SDF1-3'A. We examined the frequency of the above polymorphisms within the Cretan population, evaluating their contribution to a protective genetic background against HIV infection and progression. Two hundred blood samples were recruited at random among prospective blood donors from Crete. Genotyping was initially performed by polymerase chain reaction (PCR) analysis. CCR2 and SDF-1 PCR-amplified genomic regions were further subjected to restriction fragment length polymorphism (RFLP) analysis for genotype determination. The CCR5-delta32 allele frequency among our study group was 3.25%, although no respective homozygous samples were detected. The screening for the CCR2-64I polymorphism yielded 39 heterozygous (19.5%) and 4 homozygous (2%) subjects, revealing a CCR2-64I allele frequency of 11.75%. Among our 200 PCR-RFLP analysed samples, 73 (36.5%) were found heterozygous and 23 (11.5%) homozygous for the SDF1-3'A mutant variant. The allele frequency of the above polymorphism reached 29.75%. The frequency of the CCR5-delta32 allele among our study population seems to be remarkably lower compared to previously reported frequencies in other Caucasian groups. However, the SDF1-3'A allele frequency shows significantly higher distribution profiles within our study group compared to those observed in other Caucasian-European populations. The indicated difference could be attributed to the increased homogeneity of our population, which is well balanced and dispersed over a small geographical area. Since this polymorphism is related with delayed progression from HIV infection to AIDS, it could be used for prognostic genotyping in HIV infected Cretan individuals.

摘要

人类免疫缺陷病毒(HIV)感染流行病学中的一个有趣发现是,编码趋化因子受体及其配体的基因中的某些突变可能赋予对HIV-1感染和/或艾滋病进展的抗性。研究最频繁的突变是CCR5-Δ32、CCR2-64I和SDF1-3'A。我们研究了克里特岛人群中上述多态性的频率,评估它们对抵抗HIV感染和进展的保护性遗传背景的贡献。从克里特岛的潜在献血者中随机采集了200份血液样本。最初通过聚合酶链反应(PCR)分析进行基因分型。对CCR2和SDF-1 PCR扩增的基因组区域进一步进行限制性片段长度多态性(RFLP)分析以确定基因型。我们研究组中CCR5-Δ32等位基因频率为3.25%,尽管未检测到相应的纯合样本。CCR2-64I多态性筛查发现39名杂合子(19.5%)和4名纯合子(2%)受试者,CCR2-64I等位基因频率为11.75%。在我们分析的200个PCR-RFLP样本中,发现73个(36.5%)为SDF1-3'A突变变体的杂合子,23个(11.5%)为纯合子。上述多态性的等位基因频率达到29.75%。我们研究人群中CCR5-Δ32等位基因频率与之前报道的其他白种人群体频率相比似乎显著更低。然而,与其他欧洲白种人群体中观察到的情况相比,SDF1-3'A等位基因频率在我们研究组中的分布情况显著更高。所指出的差异可能归因于我们人群的同质性增加,该人群在一个小地理区域内平衡良好且分布分散。由于这种多态性与从HIV感染到艾滋病的进展延迟有关,它可用于对感染HIV的克里特岛个体进行预后基因分型。

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