Abstract

Host-pathogen coevolution is a major driver of species diversity, with an essential role in the generation and maintenance of genetic variation in host resistance and pathogen infectivity. Little is known about how resistance and infectivity are structured across multiple geographic scales and what eco-evolutionary processes drive these patterns. Across southern Australia, the wild flax Linum marginale is frequently attacked by its rust fungus Melampsora lini. Here, we compare the genetic and phenotypic structure of resistance and infectivity among population pairs from two regions where environmental differences associate with specific life histories and mating systems. We find that both host and pathogen populations are genetically distinct between these regions. The region with outcrossing hosts and pathogens that go through asexual cycles followed by sexual reproduction showed greater diversity of resistance and infectivity phenotypes, higher levels of resistance and less clumped within-population spatial distribution of resistance. However, in the region where asexual pathogens infect selfing hosts, pathogens were more infective and better adapted to sympatric hosts. Our findings largely agree with expectations based on the distinctly different host mating systems in the two regions, with a likely advantage for hosts undergoing recombination. For the pathogen in this system, sexual reproduction may primarily be a survival mechanism in the region where it is observed. While it appears to potentially have adverse effects on local adaptation in the short term, it may be necessary for longer-term coevolution with outcrossing hosts.

Highlights

  • Spatial and temporal heterogeneity in the genetic structure of interacting host and pathogen populations is a characteristic of natural host-pathogen systems [1], [2], [3], [4]

  • Using analysis of molecular variance (AMOVA), we found strong structure in the genetic make-up of L. marginale populations (P,0.01 for all variance components), with most molecular variation contained within individual populations (49%), whereas 34% of the variation was among populations within a region, and the remaining 17% of the variation was explained by the regional origin of the hosts

  • Identifying the processes that shape the distribution of genetic variation at different spatial and temporal scales represents a key challenge in ecology and evolutionary biology

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Summary

Introduction

Spatial and temporal heterogeneity in the genetic structure of interacting host and pathogen populations is a characteristic of natural host-pathogen systems [1], [2], [3], [4]. While spatial variation in resistance is generally observed at all spatial scales studied (reviewed in [5]), it is unclear how this structure integrates hierarchically across the multiple spatial scales of a host-pathogen interaction, eg. Within and among host populations of a region and among regions It is still mostly unclear how the spatial structure of pathogen infectivity relates to the spatial structure of host resistance for a given hostpathogen association. The consequences of spatial variation in resistance and infectivity for disease dynamics and coevolution within and across spatial scales are largely unresolved. Contrasting the patterns of spatial variation in resistance or infectivity across a range of spatial scales, and identifying biological or environmental processes that are predicted to generate these patterns constitute major goals in coevolutionary biology

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