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1型人类免疫缺陷病毒在疾病发展速度不同的儿童中的基因进化

Human immunodeficiency virus type 1 genetic evolution in children with different rates of development of disease.

作者信息

Ganeshan S, Dickover R E, Korber B T, Bryson Y J, Wolinsky S M

机构信息

Department of Medicine, Northwestern University Medical School, Chicago, Illinois 60611, USA.

出版信息

J Virol. 1997 Jan;71(1):663-77. doi: 10.1128/JVI.71.1.663-677.1997.

Abstract

The rate of development of disease varies considerably among human immunodeficiency virus type 1 (HIV-1)-infected children. The reasons for these observed differences are not clearly understood but most probably depend on the dynamic interplay between the HIV-1 quasispecies virus population and the immune constraints imposed by the host. To study the relationship between disease progression and genetic diversity, we analyzed the evolution of viral sequences within six perinatally infected children by examining proviral sequences spanning the C2 through V5 regions of the viral envelope gene by PCR of blood samples obtained at sequential visits. PCR product DNAs from four sample time points per child were cloned, and 10 to 13 clones from each sample were sequenced. Greater genetic distances relative to the time of infection were found for children with low virion-associated RNA burdens and slow progression to disease relative to those found for children with high virion-associated RNA burdens and rapid progression to disease. The greater branch lengths observed in the phylogenetic reconstructions correlated with a higher accumulation rate of nonsynonymous base substitutions per potential nonsynonymous site, consistent with positive selection for change rather than a difference in replication kinetics. Viral sequences from children with slow progression to disease also showed a tendency to form clusters that associated with different sampling times. These progressive shifts in the viral population were not found in viral sequences from children with rapid progression to disease. Therefore, despite the HIV-1 quasispecies being a diverse, rapidly evolving, and competing population of genetic variants, different rates of genetic evolution could be found under different selective constraints. These data suggest that the evolutionary dynamics exhibited by the HIV-1 quasispecies virus populations are compatible with a Darwinian system evolving under the constraints of natural selection.

摘要

1型人类免疫缺陷病毒(HIV-1)感染儿童中疾病的发展速度差异很大。目前尚不清楚这些观察到的差异的原因,但很可能取决于HIV-1准种病毒群体与宿主施加的免疫限制之间的动态相互作用。为了研究疾病进展与基因多样性之间的关系,我们通过对连续就诊时采集的血样进行PCR,检测跨越病毒包膜基因C2至V5区域的前病毒序列,分析了6名围产期感染儿童体内病毒序列的演变。每个儿童四个采样时间点的PCR产物DNA被克隆,每个样本10至13个克隆进行测序。与病毒体相关RNA负荷高且疾病进展迅速的儿童相比,病毒体相关RNA负荷低且疾病进展缓慢的儿童在感染时间点之后有更大的遗传距离。在系统发育重建中观察到的更大分支长度与每个潜在非同义位点非同义碱基替换的更高积累率相关,这与对变化的正选择一致,而不是复制动力学的差异。疾病进展缓慢的儿童的病毒序列也显示出形成与不同采样时间相关的簇的趋势。在疾病进展迅速的儿童的病毒序列中未发现病毒群体的这些渐进变化。因此,尽管HIV-1准种是一个多样、快速进化且相互竞争的遗传变异群体,但在不同的选择限制下可以发现不同的基因进化速率。这些数据表明,HIV-1准种病毒群体表现出的进化动力学与在自然选择限制下进化的达尔文系统是兼容的。

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