Host Competitive Asymmetries Accelerate Viral Evolution in a Microbe–Virus Coevolutionary System

IF 7.6 1区 环境科学与生态学 Q1 ECOLOGY
Ecology Letters Pub Date : 2025-06-19 DOI:10.1111/ele.70153
Armun Liaghat, Martin Guillemet, Rachel Whitaker, Sylvain Gandon, Mercedes Pascual
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引用次数: 0

Abstract

Microbial host populations evolve traits conferring specific resistance to viral predators via various defence mechanisms, while viruses reciprocally evolve traits to evade these defences. Such coevolutionary dynamics often involve diversification promoted by negative frequency-dependent selection. However, microbial traits conferring competitive asymmetries can induce directional selection, opposing diversification. Despite extensive research on microbe–virus coevolution, the combined effect of both host trait types and associated selection remains unclear. Using a CRISPR-mediated coevolutionary system, we examine how the co-occurrence of both trait types impacts viral evolution and persistence, previously shown to be transient and nonstationary in computational models. A stochastic model incorporating host competitive asymmetries via variation of intrinsic growth rates reveals that competitively advantaged host clades generate the majority of immune diversity. Greater asymmetries extend viral extinction times, accelerate viral adaptation locally in time and augment long-term local adaptation. These findings align with previous experiments and provide further insights into long-term coevolutionary dynamics.

Abstract Image

Abstract Image

宿主竞争不对称在微生物-病毒协同进化系统中加速病毒进化
微生物宿主群体通过各种防御机制进化出对病毒捕食者具有特定抗性的特征,而病毒则相互进化出逃避这些防御的特征。这种共同进化动力通常涉及由负频率依赖选择促进的多样化。然而,微生物性状赋予竞争不对称可以诱导定向选择,反对多样化。尽管对微生物-病毒共同进化进行了广泛的研究,但宿主性状类型和相关选择的综合影响仍不清楚。利用crispr介导的共同进化系统,我们研究了这两种性状类型的共同发生如何影响病毒的进化和持久性,这在以前的计算模型中被证明是短暂和非平稳的。一个包含宿主竞争不对称的随机模型通过内在生长速率的变化表明,竞争优势的宿主进化支产生了大部分免疫多样性。更大的不对称性延长了病毒的灭绝时间,加速了病毒的局部适应,增强了长期的局部适应。这些发现与先前的实验一致,并为长期共同进化动力学提供了进一步的见解。
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来源期刊
Ecology Letters
Ecology Letters 环境科学-生态学
CiteScore
17.60
自引率
3.40%
发文量
201
审稿时长
1.8 months
期刊介绍: Ecology Letters serves as a platform for the rapid publication of innovative research in ecology. It considers manuscripts across all taxa, biomes, and geographic regions, prioritizing papers that investigate clearly stated hypotheses. The journal publishes concise papers of high originality and general interest, contributing to new developments in ecology. Purely descriptive papers and those that only confirm or extend previous results are discouraged.
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