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A57 An evolutionary framework to guide the hunt for human dsDNA viruses

机译:A57指导寻找人类dsDNA病毒的进化框架

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摘要

It is becoming increasingly obvious that we only know a fraction of the human virome. The development of next-generation sequencing (NGS) technologies has dramatically increased our ability to hunt viruses. Yet, the small genomes and low copy numbers characteristic of most viruses make undirected (shotgun) hunts a relatively inefficient strategy. Here, we propose to speed-up the rate of double-stranded DNA (dsDNA) virus discovery by combining NGS with evolutionary thinking. dsDNA viruses are thought to have co-diverged with their hosts. As this applies to the hominine lineages (gorillas, humans, chimpanzees, and bonobos), it is theoretically possible to estimate the phylogenetic position of cryptic human viruses by identifying co-divergent viral lineages infecting non-human hominines. Where these lineages do not comprise a human-infecting counterpart, a yet-unknown human virus may be hiding. The first phase of this project will consist in the high-throughput characterization of dsDNA viruses (herpesviruses, papillomaviruses, and polyomaviruses) infecting wild gorillas, chimpanzees, and bonobos. For this, we will use an exhaustive collection of fecal samples (in terms of hominine species/sub-species diversity) and apply a discovery strategy combining in-solution capture and NGS. This strategy has been developed in the ancient DNA field but has a very broad applicability; it will constitute a nice addendum to the institute technical portfolio. Thanks to the massive amount of information collected, we will be able to reconstruct the evolutionary history of many dsDNA virus lineages and to identify those where a human virus would be expected but is still unknown. This will pave the way to the second phase of the project which will consist in a pre-oriented dsDNA human virus hunt based on the use of specific PCR systems implemented in multiplex. We expect that this project will generate an unprecedented amount of data on the processes at play along dsDNA virus evolution (co-divergence versus cross-species transmission), help determine the directionality, frequency, and timing of cross-species transmission events between hominines and unveil the existence of yet-to-be-discovered human viruses.
机译:越来越明显的是,我们只了解人类病毒的一小部分。下一代测序(NGS)技术的发展极大地提高了我们查杀病毒的能力。但是,大多数病毒的特征是小的基因组和低拷贝数使无方向性(shot弹枪)狩猎是一种相对无效的策略。在这里,我们建议通过将NGS与进化思想相结合来加快双链DNA(dsDNA)病毒的发现速度。 dsDNA病毒被认为与其宿主共同分化。由于这适用于人类谱系(大猩猩,人类,黑猩猩和bo黑猩猩),因此在理论上有可能通过确定感染非人类人类的共趋同病毒谱系来估计隐性人类病毒的系统发育位置。如果这些谱系不包含人类感染对应物,则可能隐藏着未知的人类病毒。该项目的第一阶段将包括感染野生大猩猩,黑猩猩和bo黑猩猩的dsDNA病毒(疱疹病毒,乳头瘤病毒和多瘤病毒)的高通量表征。为此,我们将详尽地收集粪便样本(就人种/亚种的多样性而言),并应用结合了溶液中捕获和NGS的发现策略。这种策略是在古代DNA领域开发的,但是具有非常广泛的适用性。它将构成研究所技术组合的一个很好的附录。多亏了收集到的大量信息,我们将能够重建许多dsDNA病毒谱系的进化历史,并识别出预期会出现但仍未知的人类病毒。这将为该项目的第二阶段铺平道路,该阶段将包括基于以多重方式实施的特定PCR系统为基础的预先定向的dsDNA人类病毒狩猎。我们希望该项目将产生关于dsDNA病毒进化过程中正在起作用的过程的前所未有的数据(共散与跨物种传播),有助于确定人与人之间跨物种传播事件的方向,频率和时间。揭露尚未发现的人类病毒的存在。

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