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Single cell analysis of lymph node tissue from HIV-1 infected patients reveals that the majority of CD4+ T-cells contain one HIV-1 DNA molecule.

机译:对HIV-1感染患者的淋巴结组织进行单细胞分析后发现,大多数CD4 + T细胞都含有一个HIV-1 DNA分子。

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摘要

Genetic recombination contributes to the diversity of human immunodeficiency virus (HIV-1). Productive HIV-1 recombination is, however, dependent on both the number of HIV-1 genomes per infected cell and the genetic relationship between these viral genomes. A detailed analysis of the number of proviruses and their genetic relationship in infected cells isolated from peripheral blood and tissue compartments is therefore important for understanding HIV-1 recombination, genetic diversity and the dynamics of HIV-1 infection. To address these issues, we used a previously developed single-cell sequencing technique to quantify and genetically characterize individual HIV-1 DNA molecules from single cells in lymph node tissue and peripheral blood. Analysis of memory and naïve CD4(+) T cells from paired lymph node and peripheral blood samples from five untreated chronically infected patients revealed that the majority of these HIV-1-infected cells (>90%) contain only one copy of HIV-1 DNA, implying a limited potential for productive recombination in virus produced by these cells in these two compartments. Phylogenetic analysis revealed genetic similarity of HIV-1 DNA in memory and naïve CD4(+) T-cells from lymph node, peripheral blood and HIV-1 RNA from plasma, implying exchange of virus and/or infected cells between these compartments in untreated chronic infection.
机译:基因重组有助于人类免疫缺陷病毒(HIV-1)的多样性。但是,生产性HIV-1重组既取决于每个感染细胞的HIV-1基因组数量,又取决于这些病毒基因组之间的遗传关系。因此,对从外周血和组织区室分离的感染细胞中原病毒的数量及其遗传关系的详细分析对于理解HIV-1重组,遗传多样性和HIV-1感染的动态非常重要。为了解决这些问题,我们使用了以前开发的单细胞测序技术来量化和遗传表征来自淋巴结组织和外周血中单细胞的单个HIV-1 DNA分子。对来自五名未经治疗的慢性感染患者的配对淋巴结和外周血样本的记忆和幼稚CD4(+)T细胞的分析显示,这些被HIV-1感染的细胞大多数(> 90%)仅包含一份HIV-1拷贝DNA,这意味着在这两个区室中这些细胞产生的病毒中生产重组的潜力有限。系统发育分析揭示了记忆中的HIV-1 DNA和淋巴结,外周血的幼稚CD4(+)T细胞和血浆中的HIV-1 RNA的遗传相似性,这意味着在未经治疗的慢性人群中这些隔室之间病毒和/或感染细胞之间的交换感染。

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