Abstract

Existing theory of host-parasite interactions has identified the genetic specificity of interaction as a key variable affecting the outcome of coevolution. The Matching Alleles (MA) and Gene For Gene (GFG) models have been extensively studied as the canonical examples of specific and non-specific interaction. The generality of these models has recently been challenged by uncovering real-world host-parasite systems exhibiting specificity patterns that fit neither MA nor GFG, and by the discovery of symbiotic bacteria protecting insect hosts against parasites. In the present paper we address both challenges, simulating a large number of non-canonical models of host-parasite interactions that explicitly incorporate symbiont-based host resistance. To assess the genetic specialisation in these hybrid models, we develop a quantitative index of specificity applicable to any coevolutionary model based on a fitness matrix. We find qualitative and quantitative effects of host-parasite and symbiont-parasite specificities on genotype frequency dynamics, allele survival, and mean host and parasite fitnesses.

Highlights

  • Parasitism is one of the main lifestyles in nature and a major source of evolutionary pressure

  • We find that specificity as defined in this paper strongly influences important coevolutionary outcomes of the models, such as the genotype frequency dynamics, maintenance of allelic diversity and mean host and parasite fitness

  • Genetic specialisation has been recognised in the literature on host-parasite interactions as a fundamental concept in its own right [22]

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Summary

Introduction

Parasitism is one of the main lifestyles in nature and a major source of evolutionary pressure. Despite its central place in evolutionary ecology, the details of the genetic architecture underlying resistance and infectivity are not known for most host-parasite associations. Mathematical models of host-parasite coevolution compensate for the missing data by making explicit, first-principle assumptions about the interaction of host and parasite genotypes. Two such classic assumptions, and two classic families of models, are known as Matching Alleles (MA) and Gene For Gene (GFG). In the GFG models the parasite carrying all virulence alleles takes over the population, at least until costs of infectivity and resistance are assumed [3,6]

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