Abstract

BackgroundNumerous empirical studies suggest that hosts and microbes exert reciprocal selective effects on their ecological partners. Nonetheless, we still lack an explicit framework to model the dynamics of both hosts and microbes under selection. In a previous study, we developed an agent-based forward-time computational framework to simulate the neutral evolution of host-associated microbial communities in a constant-sized, unstructured population of hosts. These neutral models allowed offspring to sample microbes randomly from parents and/or from the environment. Additionally, the environmental pool of available microbes was constituted by fixed and persistent microbial OTUs and by contributions from host individuals in the preceding generation.MethodsIn this paper, we extend our neutral models to allow selection to operate on both hosts and microbes. We do this by constructing a phenome for each microbial OTU consisting of a sample of traits that influence host and microbial fitnesses independently. Microbial traits can influence the fitness of hosts (“host selection”) and the fitness of microbes (“trait-mediated microbial selection”). Additionally, the fitness effects of traits on microbes can be modified by their hosts (“host-mediated microbial selection”). We simulate the effects of these three types of selection, individually or in combination, on microbiome diversities and the fitnesses of hosts and microbes over several thousand generations of hosts.ResultsWe show that microbiome diversity is strongly influenced by selection acting on microbes. Selection acting on hosts only influences microbiome diversity when there is near-complete direct or indirect parental contribution to the microbiomes of offspring. Unsurprisingly, microbial fitness increases under microbial selection. Interestingly, when host selection operates, host fitness only increases under two conditions: (1) when there is a strong parental contribution to microbial communities or (2) in the absence of a strong parental contribution, when host-mediated selection acts on microbes concomitantly.ConclusionsWe present a computational framework that integrates different selective processes acting on the evolution of microbiomes. Our framework demonstrates that selection acting on microbes can have a strong effect on microbial diversities and fitnesses, whereas selection on hosts can have weaker outcomes.

Highlights

  • Numerous empirical studies suggest that hosts and microbes exert reciprocal selective effects on their ecological partners

  • In this paper, when we model these neutral processes with very large numbers of microbes and hosts, we find no evidence that microbial diversity is depressed under neutral conditions even when parental contributions are high (Figs. 3 and 4)

  • Our results explain why opportunistic acquisition of microbes can still deliver functional benefits to hosts. Previous studies suggest both hosts and microbes exert these selective filters on their partners, and these filters in turn may influence the evolution of these hostassociated microbial communities or microbiomes

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Summary

Introduction

Numerous empirical studies suggest that hosts and microbes exert reciprocal selective effects on their ecological partners. We developed an agent-based forward-time computational framework to simulate the neutral evolution of host-associated microbial communities in a constant-sized, unstructured population of hosts. These neutral models allowed offspring to sample microbes randomly from parents and/or from the environment. In a recent paper [1], we developed an agent-based framework to model the evolution of host-associated microbial communities (i.e., microbiomes), in the absence of any fitness costs or benefits to hosts or microbes, and subject only to the stochasticity of sampling. It is reasonable to extend the neutral model of microbial evolution to allow selective effects: conceivably, hosts with beneficial microbes are more likely to succeed in competition with hosts that have fewer such microbes; it is likely that microbes that are able to withstand the selective filters imposed by environments within hosts, and host antimicrobial defenses, are able to persist within individual hosts

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