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Evolution of intrahost HIV-1 genetic diversity during chronic infection

机译:慢性感染期间宿主内HIV-1遗传多样性的演变

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HIV-1 is one of the fastest evolving entities known. Given that census population sizes of HIV-1 within individuals are much greater than the inverse mutation rate, every possible single point mutation in the viral genome occurs each generation. This enormous capability to generate genetic variation allows for escape from immune surveillance and antiviral therapy. However, compared to this potential, populations of HIV-1 within individuals exhibit little genetic variation. This discrepancy between the known mutation rate of HIV-1 and the average level of genetic variation in the env gene observed in vivo is reflected in comparisons of the actual numbers of productively infected cells, estimated as 10(7), and the effective population size, estimated as 10(3). Using approximate Bayesian computation, we evaluated several hypotheses based on a variety of selective and demographic processes to explain the low effective population size of HIV-1. Of the models we examined, the metapopulation model, in which HIV-1 evolves within an individual as a large collection of small subpopulations subject to frequent migration, extinction, and recolonization, was most consistent with the observed levels of genetic variation and the average frequencies of those variants. The metapopulation model links previous studies of viral dynamics and population genetics.
机译:HIV-1是已知发展最快的实体之一。鉴于人口中HIV-1的人口普查规模远大于反向突变率,病毒基因组中每个可能的单点突变都会在每一代发生。这种巨大的产生基因变异的能力可以避免免疫监视和抗病毒治疗。但是,与这种潜力相比,个体内的HIV-1群体几乎没有遗传变异。 HIV-1已知突变率与体内观察到的env基因平均遗传变异水平之间的差异反映在生产性感染细胞的实际数量(估计为10(7))与有效种群数量的比较中,估计为10(3)。使用近似贝叶斯计算,我们基于各种选择性和人口统计学过程评估了几种假设,以解释HIV-1的低有效种群规模。在我们研究的模型中,HIV-1在个体中以大量小亚种群的形式在个体内进化的频繁迁移,灭绝和再定殖的传播种群模型,与观察到的遗传变异水平和平均频率最一致这些变体中。种群模型将病毒动力学和种群遗传学的先前研究联系起来。

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