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Genomic Analysis of HIV Type 1 Strains Derived from a Mother and Child Pair of Long-Term Nonprogressors

机译:一对长期非进行母婴配对的HIV 1型菌株的基因组分析

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摘要

To investigate the viral features of long-term nonprogressive HIV-1 infection and the selection of viral genomes, we studied serial complete HIV-1 sequences obtained from a mother–child pair, both long-term nonprogressors. Analysis of four genomic sequences demonstrated that all viral genes were intact, lacking major deletions or premature stop codons to easily explain the slow disease progression. These data suggest that viral attenuation, if present, was caused by subtle sequence variations or virus–host interactions. Serial sequences from an HIV-1-infected mother–child pair afforded us the opportunity to examine the immune selection of HIV-1 sequences years after transmission between individuals. We demonstrated that the daughter's strains were most likely subjected to immunoselection or immunoediting according to the presence of novel MHC class I alleles that differed between mother and daughter. An analysis of nef-specific cytotoxic T-lymphocyte responses in the child, whose HIV-1 nef sequence differed from the maternal nef, supported this interpretation. This study highlights the potential of full genome analysis in the investigation of pathogenesis and immune selection during HIV-1 evolution.
机译:为了研究长期非进行性HIV-1感染的病毒特征以及病毒基因组的选择,我们研究了从母婴对获得的一系列完整HIV-1序列,这两个都是长期非进展性的。对四个基因组序列的分析表明,所有病毒基因都是完整的,缺少主要的缺失或过早的终止密码子,可以轻松地解释疾病的缓慢发展。这些数据表明,病毒衰减(如果存在)是由细微的序列变异或病毒-宿主相互作用引起的。 HIV-1感染的母子对的序列序列为我们提供了在个体之间传播数年后检查HIV-1序列免疫选择的机会。我们证明女儿的菌株最有可能根据新的MHC I类等位基因的存在而进行免疫选择或免疫编辑,这些MHC I类等位基因在母女之间有所不同。对HIV-1 nef序列不同于母体nef的儿童中nef特异性细胞毒性T淋巴细胞反应的分析支持了这一解释。这项研究强调了全基因组分析在HIV-1进化过程中的发病机理和免疫选择研究中的潜力。

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