Data from: Genes of the major histocompatibility complex highlight interactions of the innate and adaptive immune system
Data files
Sep 01, 2017 version files 646.98 MB
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454-input - primersJMHC.xls
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454-input - R1 - 1.TCA.454Reads.fna
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454-input - R1 - 2.TCA.454Reads.fna
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454-input - R1 - Primertags.txt
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454-input - R2 - 1.TCA.454Reads.fna
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454-input - R2 - 2.TCA.454Reads.fna
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454-input - R2 - Primertags.txt
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454-output - R1 output.txt
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454-output - R1.sqlite
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454-output - R2 output.txt
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454-output - R2.sqlite
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Genotype and phenotype table PeerJ 082017.xlsx
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Microsatellite genotype table.xlsx
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Sequence allignment - All 59 functional MHC alleles from this study.fas
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Sequence allignment - All 85 MHC alleles from this study.fas
Abstract
Background: A well-functioning immune defence is crucial for fitness, but our knowledge about the immune system and its complex interactions is still limited. Major histocompatibility complex (MHC) molecules are involved in T-cell mediated adaptive immune responses, but MHC is also highly upregulated during the initial innate immune response. The aim of our study was therefore to determine to what extent the highly polymorphic MHC is involved in interactions of the innate and adaptive immune defence and if specific functional MHC alleles (FA) or heterozygosity at the MHC are more important. Methods: To do this we used captive house sparrows (Passer domesticus) to survey MHC diversity and immune function controlling for several environmental factors. MHC class I alleles were identified using parallel amplicon sequencing and to mirror immune function, several immunological tests that correspond to the innate and adaptive immunity were conducted. Results: Our results reveal that MHC was linked to all immune tests, highlighting its importance for the immune defence. While all innate responses were associated with one single FA, adaptive responses (cell-mediated and humoral) were associated with several different alleles. Discussion: We found that repeated injections of an antibody in nestlings and adults were linked to different FA and hence might affect different areas of the immune system. Also, individuals with a higher number of different FA produced a smaller secondary response, indicating a disadvantage of having numerous MHC alleles. These results demonstrate the complexity of the immune system in relation to the MHC and lay the foundation for other studies to further investigate this topic.