在 CRISPR 介导的微生物-病毒协同进化过程中,病毒驱动的间断演替产生了动态交替。

IF 3.7 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Journal of The Royal Society Interface Pub Date : 2024-08-01 Epub Date: 2024-08-21 DOI:10.1098/rsif.2024.0195
Armun Liaghat, Jiayue Yang, Rachel Whitaker, Mercedes Pascual
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引用次数: 0

摘要

在以前的计算模型中,具有CRISPR-Cas免疫能力的溶解病毒和微生物的共同进化动态表现出宿主对病毒增殖的持续控制和病毒大流行之间的交替。这些交替动态尚未在其他宿主-病原体系统中观察到。在这里,我们用一个随机生态进化模型来解决控制的崩溃和向大规模爆发的过渡问题。我们确定了宿主密度依赖性竞争在病毒驱动的点状演替中的作用,以及在控制阶段集中逃逸途径的相关多样性趋势。利用感染和逃逸网络,我们推导出病毒出现概率,其波动的规模和频率不断增加,是大爆发的特征。我们探讨了交替概率与病毒逃逸概率和宿主竞争相关的非维度参数的函数关系。我们的研究结果表明,宿主竞争和病毒多样化之间出现的反馈是如何使宿主免疫结构变得脆弱,从而促进向大规模流行病的动态过渡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Punctuated virus-driven succession generates dynamical alternations in CRISPR-mediated microbe-virus coevolution.

The coevolutionary dynamics of lytic viruses and microbes with CRISPR-Cas immunity exhibit alternations between sustained host control of viral proliferation and major viral epidemics in previous computational models. These alternating dynamics have yet to be observed in other host-pathogen systems. Here, we address the breakdown of control and transition to large outbreaks with a stochastic eco-evolutionary model. We establish the role of host density-dependent competition in punctuated virus-driven succession and associated diversity trends that concentrate escape pathways during control phases. Using infection and escape networks, we derive the viral emergence probability whose fluctuations of increasing size and frequency characterize the approach to large outbreaks. We explore alternation probabilities as a function of non-dimensional parameters related to the probability of viral escape and host competition. Our results demonstrate how emergent feedbacks between host competition and viral diversification render the host immune structure fragile, potentiating a dynamical transition to large epidemics.

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来源期刊
Journal of The Royal Society Interface
Journal of The Royal Society Interface 综合性期刊-综合性期刊
CiteScore
7.10
自引率
2.60%
发文量
234
审稿时长
2.5 months
期刊介绍: J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.
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