Evolutionary Genetics, Leibniz-Institute for Zoo and Wildlife Research, Berlin, Germany.
PLoS One. 2012;7(2):e31820. doi: 10.1371/journal.pone.0031820. Epub 2012 Feb 28.
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.
宿主对不同寄生虫类型的易感性差异在很大程度上取决于免疫基因和寄生虫抗原之间的匹配程度。具体来说,主要组织相容性复合体 (MHC) 的可变基因在寄生虫防御中起着主要作用。然而,由于缺乏涉及多种寄生虫感染及其在内部竞争的研究,因此仍然不太了解野生种群中的潜在遗传机制。为了深入了解这些复杂的关联,我们对条纹鼠(Rhabdomys pumilio)的 439 个基因分型个体的胃肠道线虫全记录进行了分析。我们使用两种不同的多元方法,根据维持 MHC 多样性的主要病原体驱动选择假设和寄生虫种间协同进化效应,测试了 MHC 类 II DRB 基因型与多种线虫之间的关联。前者包括对“杂合优势”的研究,或者其特定形式“分歧等位基因优势”,这是由高度不同的等位基因引起的,以及由“稀有等位基因优势”(即负“频率依赖性选择”)选择的特定 MHC 等位基因的可能影响。广义线性混合模型 (GLMM) 和共惰性 (COIA) 分析的结合使得即使在种群和个体水平上存在 I 型错误的风险,也可以考虑多种寄生虫物种。我们没有发现任何“杂合”优势的证据,但支持“分歧等位基因”优势和感染强度。此外,这两种方法都证明了特定 MHC 等位基因与某些寄生虫物种之间存在正向和负向关联的高度一致性。此外,某些 MHC 等位基因与一种以上的寄生虫物种相关,表明 MHC 基因与寄生虫之间存在多对多的协同进化。最常见的等位基因 Rhpu-DRB*38 显示出多效性,涉及三种线虫物种。我们的研究表明,在寄生虫检测方面,特异性和一般性 MHC 等位基因共存,这可能是维持 MHC 多态性的一个重要特征。