Abstract

Differences in host susceptibility to different parasite types are largely based on the degree of matching between immune genes and parasite antigens. Specifically the variable genes of the major histocompatibility complex (MHC) play a major role in the defence of parasites. However, underlying genetic mechanisms in wild populations are still not well understood because there is a lack of studies which deal with multiple parasite infections and their competition within. To gain insights into these complex associations, we implemented the full record of gastrointestinal nematodes from 439 genotyped individuals of the striped mouse, Rhabdomys pumilio. We used two different multivariate approaches to test for associations between MHC class II DRB genotype and multiple nematodes with regard to the main pathogen-driven selection hypotheses maintaining MHC diversity and parasite species-specific co-evolutionary effects. The former includes investigations of a ‘heterozygote advantage’, or its specific form a ‘divergent-allele advantage’ caused by highly dissimilar alleles as well as possible effects of specific MHC-alleles selected by a ‘rare allele advantage’ ( = negative ‘frequency-dependent selection’). A combination of generalized linear mixed models (GLMMs) and co-inertia (COIA) analyses made it possible to consider multiple parasite species despite the risk of type I errors on the population and on the individual level. We could not find any evidence for a ‘heterozygote’ advantage but support for ‘divergent-allele’ advantage and infection intensity. In addition, both approaches demonstrated high concordance of positive as well as negative associations between specific MHC alleles and certain parasite species. Furthermore, certain MHC alleles were associated with more than one parasite species, suggesting a many-to-many gene-parasite co-evolution. The most frequent allele Rhpu-DRB*38 revealed a pleiotropic effect, involving three nematode species. Our study demonstrates the co-existence of specialist and generalist MHC alleles in terms of parasite detection which may be an important feature in the maintenance of MHC polymorphism.

Highlights

  • More than 50% of the known species on this planet are parasites or pathogens of some form [1]

  • Genetic control of worm burden is likely to be polygenic and it is acknowledged that the immune response is regulated by interleukin receptor genes [8], [9] recent studies have emphasized the importance of immune genes of the major histocompatibility complex (MHC)

  • A more mechanistic explanation suggests that those individuals possessing highly dissimilar MHC alleles potentially bind an even broader range of antigenic peptides heterozygotes with less dissimilar alleles which may confer a broader immune competence in the case of varying or multiple infestations (‘divergent allele advantage hypothesis’, [12,13,14,15])

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Summary

Introduction

More than 50% of the known species on this planet are parasites or pathogens of some form [1]. It is known that intestinal worm infections generally cause a strong host immune response e.g. Many studies give evidence that high MHC polymorphism is maintained by pathogen-driven selection either due to the effects of specific MHC-alleles (‘rare allele advantage hypothesis’ or ‘frequency-dependent selection’, [11]) or an advantage of heterozygote individuals (‘heterozygote advantage’, [12]). A more mechanistic explanation suggests that those individuals possessing highly dissimilar MHC alleles potentially bind an even broader range of antigenic peptides heterozygotes with less dissimilar alleles which may confer a broader immune competence in the case of varying or multiple infestations (‘divergent allele advantage hypothesis’, [12,13,14,15]). Despite a tremendous effort identifying the relative importance of these mechanisms, the complex dynamics of parasite-host-interactions still remain elusive [16], [17]

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