Abstract

To understand the mechanisms of antagonistic coevolution, it is crucial to identify the genetics of parasite resistance. In the Daphnia magna–Pasteuria ramosa host–parasite system, the most important step of the infection process is the one in which P. ramosa spores attach to the host’s foregut. A matching-allele model (MAM) describes the host–parasite genetic interactions underlying attachment success. Here we describe a new P. ramosa genotype, P15, which, unlike previously studied genotypes, attaches to the host’s hindgut, not to its foregut. Host resistance to P15 attachment shows great diversity across natural populations. In contrast to P. ramosa genotypes that use foregut attachment, P15 shows some quantitative variation in attachment success and does not always lead to successful infections, suggesting that hindgut attachment represents a less-efficient infection mechanism than foregut attachment. Using a Quantitative Trait Locus (QTL) approach, we detect two significant QTLs in the host genome: one that co-localizes with the previously described D. magna PR locus of resistance to foregut attachment, and a second, major QTL located in an unlinked genomic region. We find no evidence of epistasis. Fine mapping reveals a genomic region, the D locus, of ~13 kb. The discovery of a second P. ramosa attachment site and of a novel host-resistance locus increases the complexity of this system, with implications for both for the coevolutionary dynamics (e.g., Red Queen and the role of recombination), and for the evolution and epidemiology of the infection process.

Highlights

  • Host–parasite interactions are thought to be one of the main drivers of organismic evolution, promoting both diversification and genetic diversity (Schmid-Hempel 2011)

  • We tested whether this held true for P. ramosa P15 attachment to the D. magna hindgut (Table S2) by using P15 attachmentpositive and P15 attachment-negative clones from a standing Quantitative Trait Locus (QTL) panel (Routtu et al 2014) and exposing 40 host clones to infectious P15 spores

  • Our previous picture relied on the assumption of a linear stepwise infection process: (1) host–parasite encounter, (2) activation of the parasite endospore, (3) attachment to the host cuticle, (4) penetration of the host, (5) early and (6) late within-host growth phase, and (7) host death (Ebert et al 2016, Hall et al 2017)

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Summary

Introduction

Host–parasite interactions are thought to be one of the main drivers of organismic evolution, promoting both diversification and genetic diversity (Schmid-Hempel 2011). The theory is that hosts evolve to minimize fitness costs associated with parasitism, whereas parasites evolve to maximize fitness while exploiting the host and avoiding its defense mechanisms.

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