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首页> 外文期刊>BMC research notes >Distribution of CCR5-Delta32, CCR5 promoter 59029 A/G, CCR2-64I and SDF1-3’A genetic polymorphisms in HIV-1 infected and uninfected patients in the West Region of Cameroon
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Distribution of CCR5-Delta32, CCR5 promoter 59029 A/G, CCR2-64I and SDF1-3’A genetic polymorphisms in HIV-1 infected and uninfected patients in the West Region of Cameroon

机译:喀麦隆西部地区HIV-1感染和未感染患者中CCR5-Delta32,CCR5启动子59029 A / G,CCR2-64I和SDF1-3’A遗传多态性的分布

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摘要

Background Genetic variants of the genes encoding Human Immunodeficiency Virus -1 ( HIV-1 ) co-receptors and their ligands, like CC-Chemokine Receptor 5 delta 32 mutation ( CCR5 - Delta32 ), CCR5 promoter A / G (Adenine/Guanine), CC-Chemokine Receptor 2 mutation 64 isoleucine ( CCR2 - 64I ) and the Stromal cell-derived Factor 3’A mutation ( SDF1 - 3 ’ A ), are involved in the susceptibility to HIV-1 infection and progression. The prevalence of these mutations varies by Region. However, little is known about their distribution in the population of Dschang, located in the West Region of Cameroon. The prevalence of HIV in the West Region of Cameroon is lower than elsewhere in Cameroon. The objectives of this study were to determine the distribution of four AIDS Related Gene (ARG) variants in HIV-infected and non-infected population of Cameroon especially in the West Region and to estimate the contribution of these variants to the susceptibility or resistance to HIV infection. We also aimed to evaluate the effectiveness of genotyping using dried blood spot (DBS) samples. Methods A total of 179 participants were recruited from two hospitals in Dschang in the West Region of Cameroon. Their genotypes for CCR5 - Delta32 , CCR5 promoter 59029A / G , CCR2 - 64I and SDF1 - 3 ’ A were analyzed using polymerase chain reaction (PCR) and restriction fragment length polymorphisms. Results A total of 179 participants were enrolled in the study. Among them, 32 (17.9%) were HIV positive and 147 (82.1%) were HIV negative. The allelic frequencies of these genes were: 0%, 49.72%, 17.6% and 100% respectively for CCR5 - Delta32 , CCR5 promoter 59029A / G , CCR2 - 64I and SDF1 - 3 ’ A . No individual was found to carry the CCR5 - Delta 32 mutation. All participants recruited were heterozygous for the SDF1 - 3 ’ A allele. Conclusion Our data suggest that the CCR5 - Delta32 cannot account for the protection as it was completely absent in our population. SDF1 - 3 ’ A variants, may be in association with other polymorphisms, may account for the overall protection from HIV-1 infection in participants recruited as everyone carries this allele. The CCR5 promoter 59029 G / G genotype may be associated with the risk for HIV-1 infection in this population, while the CCR2 - 64I (A/A genotype) may account for the protection against HIV infection. The results of genotyping from fresh blood and DBS were comparable.
机译:背景编码人类免疫缺陷病毒-1(HIV-1)共受体及其配体的基因的遗传变异,例如CC-趋化因子受体5 delta 32突变(CCR5-Delta32),CCR5启动子A / G(腺嘌呤/鸟嘌呤), CC-趋化因子受体2突变64异亮氨酸(CCR2-64I)和基质细胞衍生的3'A因子突变(SDF1-3'A)参与了HIV-1感染和进展的易感性。这些突变的发生率因地区而异。但是,关于它们在喀麦隆西部地区Dschang人口中的分布情况知之甚少。喀麦隆西部地区的艾滋病毒流行率低于喀麦隆其他地区。这项研究的目的是确定四种艾滋病相关基因(ARG)变异在喀麦隆的HIV感染和未感染人群中的分布,尤其是在西部地区,并评估这些变异对HIV易感性或抗药性的贡献感染。我们还旨在评估使用干血斑(DBS)样本进行基因分型的有效性。方法从喀麦隆西部地区Dschang的两家医院招募了179名参与者。使用聚合酶链反应(PCR)和限制性片段长度多态性分析了CCR5-Delta32,CCR5启动子59029A / G,CCR2-64I和SDF1-3’的基因型。结果共有179名参与者参加了该研究。其中,艾滋病毒呈阳性的有32(17.9%),艾滋病毒呈阴性的是147(82.1%)。这些基因的等位基因频率分别为:CCR5-Delta32,CCR5启动子59029A / G,CCR2-64I和SDF1-3’A分别为0%,49.72%,17.6%和100%。没有人发现携带CCR5-Delta 32突变。招募的所有参与者均为SDF1-3’A等位基因的杂合子。结论我们的数据表明CCR5-Delta32无法说明保护作用,因为它在我们的人群中是完全不存在的。 SDF1-3’A变异体可能与其他多态性有关,可能解释了因每个人都携带该等位基因而招募的参与者对HIV-1感染的总体保护作用。 CCR5启动子59029 G / G基因型可能与该人群中HIV-1感染的风险有关,而CCR2-64I(A / A基因型)可能是针对HIV感染的保护。从新鲜血液和DBS进行基因分型的结果相当。

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