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Niche adaptation and viral transmission of human papillomaviruses from archaic hominins to modern humans

机译:人类乳头瘤病毒从古人类素到现代人类的生态位适应和病毒传播

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Recent discoveries on the origins of modern humans from multiple archaic hominin populations and the diversity of human papillomaviruses (HPVs) suggest a complex scenario of virus-host evolution. To evaluate the origin of HPV pathogenesis, we estimated the phylogeny, timing, and dispersal of HPV16 variants using a Bayesian Markov Chain Monte Carlo framework. To increase precision, we identified and characterized non-human primate papillomaviruses from New and Old World monkeys to set molecular clock models. We demonstrate specific host niche adaptation of primate papillomaviruses with subsequent coevolution with their primate hosts for at least 40 million years. Analyses of 212 HPV16 complete genomes and 3582 partial sequences estimated ancient divergence of HPV16 variants (between A and BCD lineages) from their most recent common ancestors around half a million years ago, roughly coinciding with the timing of the split between archaic Neanderthals and modern Homo sapiens, and nearly three times longer than divergence times of modern Homo sapiens. HPV16 A lineage variants were significantly underrepresented in present African populations, whereas the A sublineages were highly prevalent in European (A1-3) and Asian (A4) populations, indicative of viral sexual transmission from Neanderthals to modern non-African humans through multiple interbreeding events in the past 80 thousand years. Remarkably, the human leukocyte antigen B*07:02 and C*07:02 alleles associated with increased risk in cervix cancer represent introgressed regions from Neanderthals in present-day Eurasians. The archaic hominin-host-switch model was also supported by other HPV variants. Niche adaptation and virus-host codivergence appear to influence the pathogenesis of papillomaviruses.
机译:关于现代人类起源的最新发现来自多个古老的人类素族,以及人类乳头瘤病毒(HPV)的多样性提示了病毒宿主进化的复杂情况。为了评估HPV发病机制的起源,我们使用贝叶斯马尔可夫链蒙特卡洛框架估计了HPV16变异的系统发生,时间安排和扩散。为了提高精度,我们从新大陆和旧世界的猴子中鉴定并鉴定了非人类的灵长类乳头瘤病毒,以设置分子时钟模型。我们展示了灵长类乳头瘤病毒的特定宿主生态位适应性,随后与其灵长类宿主共进化至少4000万年。对212个HPV16完整基因组和3582个部分序列的分析估计,大约在一百万年前,HPV16变体(在A和BCD谱系之间)与其最近的共同祖先之间的古代差异,大致与古老的尼安德特人和现代人分裂的时间相吻合。并比现代智人的发散时间长将近三倍。 HPV16 A谱系变异在目前的非洲人群中代表性不足,而A子谱系在欧洲(A1-3)和亚洲(A4)人群中高度流行,表明通过多次杂交事件从尼安德特人向现代非非洲人进行了病毒性传播在过去的八万年中值得注意的是,与子宫颈癌风险增加相关的人白细胞抗原B * 07:02和C * 07:02等位基因代表了当今欧亚大陆中尼安德特人的渗入区域。其他HPV变体也支持古朴的人激素-宿主-交换模型。生态位适应和病毒宿主共存似乎影响乳头瘤病毒的发病机理。

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