Sustained beneficial infections: priority effects, competition, and specialization drive patterns of association in intracellular mutualisms

Author:

Hill Malcolm,Lawson Barry,Cain John W.,Rahman Nasheya,Toolsidass Shiv,Wang Tongyu,Geraghty Sara,Raymundo Eberardo,Hill April

Abstract

Intracellular symbioses provide a useful system for exploring evolutionary and ecological forces that shape mutualistic partnerships. Within- and among-host competitiveness driven by different strategies that symbionts adopt as they transfer materials to the host across a sub-cellular membrane might explain patterns of host:symbiont association observed in natural systems. We tested the hypothesis that different translocation strategies employed by symbionts affect their ability to occupy host habitats using two distinct modeling approaches. The first involved constructing a deterministic, Lotka-Volterra-type model with two symbiont species competing for access to a single host. The model recovered expected behaviors of co-occupancy/coinfection as well as competitive exclusion. However, a specialization coefficient allowed advantages to accrue to one of the symbionts and permitted otherwise inferior competitors to displace superior competitors. The second approach involved developing and implementing a detailed, highly configurable, and realstic agent-based model (ABM), facilitating experimentation of multiple symbiont strategies in competition simultaneously. The ABM emphasizes bidirectional movement of materials between symbiont and host (e.g., photosynthate from algae to heterotrophic host). Competitive interactions between symbionts based on simple strategies led to exclusion of the inferior symbiont or co-occupancy of the host. As in the first model, inferior competitors could overtake superior competitors when “affinity” terms (i.e., specialization) were included in the model. Both models lay bare the importance of coevolutionary specialization as a selectively advantageous strategy, and they offer a new conceptual framework for interpreting the dynamic patterns observed in extant host and mutualist associations by challenging the idea of “host control” of outcomes, and identifying specific points where coevolutionary specialization might accrue.

Publisher

Frontiers Media SA

Subject

Ecology,Ecology, Evolution, Behavior and Systematics

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3