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暴露于人类免疫缺陷病毒(HIV)的血清阴性个体中CCR 5基因的分子特征分析。

Molecular characterization of the CCR 5 gene in seronegative individuals exposed to human immunodeficiency virus (HIV).

作者信息

Rugeles M T, Solano F, Díaz F J, Bedoya V I, Patiño P J

机构信息

Immunovirology Group, Laboratorio de Virologia, Facultdad de Medicina, Universidad de Antioquia, A.A. 1226, Medellin, Colombia.

出版信息

J Clin Virol. 2002 Jan;23(3):161-9. doi: 10.1016/s1386-6532(01)00219-0.

Abstract

BACKGROUND

Both clinical and laboratory evidence in exposed seronegative (ESN) individuals to human HIV-1 has suggested the existence of mechanisms of natural resistance to the infection. A 32 base-pair deletion in the gene that codes for the CCR5, which is the main coreceptor for HIV-1, confers a high degree of resistance to HIV-1 infection. However, the genotype Delta32/Delta32 is present only in 2-4% of Caucasoid ESN individuals suggesting the existence of other mechanisms of protection. Mutations different from Delta32 have also been proposed as playing a role in resistance/susceptibility to this infection.

OBJECTIVE

To screen for different mutations along the entire coding region of the ccr5 gene that can potentially explain the persistent seronegativity in a group of ESN individuals.

STUDY DESIGN

Of a total of 86 individuals analyzed for Delta32 mutation by the PCR technique, 36 scored HIV seropositive (SP) and 50 were ESN. The entire group of ESN individuals was screened for other mutations in the ccr5 gene by single strand conformational polymorphism (SSCP) and DNA sequencing.

RESULTS

The frequency of the mutant allele Delta32 was 4% (4/100) for ESN individuals and 4.2% (3/72) for SP individuals. The homozygous mutant genotype (Delta32/Delta32) was found in only 2% (1/50) of ESN individuals, but in no SP individuals. The heterozygous genotype was found in 8.3% (3/36) of SP individuals and in 4% (2/50) of ESN individuals. The differences in the allelic and genotypic frequencies among the groups were not statistically significant. A comparison between the observed and the expected genotypic frequencies showed that they were significantly different for the ESN group, suggesting a protective, yet indirect effect of the mutant genotype.

CONCLUSIONS

The screening of the entire coding region of the ccr5 gene in all ESN did not revealed no other mutations that could account for resistance to HIV-1 infection. Although the CCR5 molecule is the most important coreceptor for HIV-1, mutations in this gene do not account for most of the cases of natural resistance to this virus that have so far been reported.

摘要

背景

暴露于人类HIV-1的血清阴性(ESN)个体的临床和实验室证据均表明存在对该感染的天然抵抗机制。编码CCR5(HIV-1的主要共受体)的基因中32个碱基对的缺失赋予对HIV-1感染的高度抗性。然而,Delta32/Delta32基因型仅存在于2%至4%的白种人ESN个体中,这表明存在其他保护机制。与Delta32不同的突变也被认为在对这种感染的抗性/易感性中起作用。

目的

筛查ccr5基因整个编码区域中可能解释一组ESN个体持续血清阴性的不同突变。

研究设计

通过PCR技术对86名个体进行Delta32突变分析,其中36名HIV血清学阳性(SP),50名是ESN。通过单链构象多态性(SSCP)和DNA测序对整个ESN个体组进行ccr5基因其他突变的筛查。

结果

ESN个体中突变等位基因Delta32的频率为4%(4/100),SP个体中为4.2%(3/72)。纯合突变基因型(Delta32/Delta32)仅在2%(1/50)的ESN个体中发现,而在SP个体中未发现。杂合基因型在8.3%(3/36)的SP个体和4%(2/50)的ESN个体中发现。各组之间等位基因和基因型频率的差异无统计学意义。观察到的和预期的基因型频率之间的比较表明,ESN组存在显著差异,提示突变基因型具有保护性但间接的作用。

结论

对所有ESN个体的ccr5基因整个编码区域进行筛查未发现可解释对HIV-1感染抗性的其他突变。尽管CCR5分子是HIV-1最重要的共受体,但该基因中的突变并不能解释迄今为止报道的大多数对该病毒的天然抗性病例。

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