Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Department of Ecology and Evolution, University of Chicago, Chicago, IL, USA.
Nat Ecol Evol. 2020 Dec;4(12):1650-1660. doi: 10.1038/s41559-020-01312-z. Epub 2020 Oct 19.
As a heritable sequence-specific adaptive immune system, CRISPR-Cas is a powerful force shaping strain diversity in host-virus systems. While the diversity of CRISPR alleles has been explored, the associated structure and dynamics of host-virus interactions have not. We explore the role of CRISPR in mediating the interplay between host-virus interaction structure and eco-evolutionary dynamics in a computational model and compare the results with three empirical datasets from natural systems. We show that the structure of the networks describing who infects whom and the degree to which strains are immune, are respectively modular (containing groups of hosts and viruses that interact strongly) and weighted-nested (specialist hosts are more susceptible to subsets of viruses that in turn also infect the more generalist hosts with many spacers matching many viruses). The dynamic interplay between these networks influences transitions between dynamical regimes of virus diversification and host control. The three empirical systems exhibit weighted-nested immunity networks, a pattern our theory shows is indicative of hosts able to suppress virus diversification. Previously missing from studies of microbial host-pathogen systems, the immunity network plays a key role in the coevolutionary dynamics.
作为一种可遗传的序列特异性适应性免疫系统,CRISPR-Cas 是塑造宿主-病毒系统菌株多样性的强大力量。虽然已经探索了 CRISPR 等位基因的多样性,但宿主-病毒相互作用的相关结构和动态尚未得到探索。我们在计算模型中探索了 CRISPR 在介导宿主-病毒相互作用结构与生态进化动力学之间相互作用中的作用,并将结果与来自自然系统的三个经验数据集进行了比较。我们表明,描述谁感染谁以及菌株免疫程度的网络结构分别是模块化的(包含相互强烈作用的宿主和病毒群)和加权嵌套的(专门的宿主更容易受到特定病毒子集的感染,而这些病毒反过来也更容易感染具有许多与许多病毒匹配的间隔子的更普遍的宿主)。这些网络之间的动态相互作用影响病毒多样化和宿主控制的动态转变。这三个经验系统表现出加权嵌套的免疫网络,我们的理论表明,这种模式表明宿主能够抑制病毒多样化。在微生物宿主-病原体系统的研究中以前没有出现过,免疫网络在共进化动力学中起着关键作用。