Literature DB >> 15058398

Major histocompatibility complex diversity influences parasite resistance and innate immunity in sticklebacks.

Joachim Kurtz1, Martin Kalbe, Peter B Aeschlimann, Michael A Häberli, K Mathias Wegner, Thorsten B H Reusch, Manfred Milinski.   

Abstract

Proteins of the major histocompatibility complex (MHC) play a central role in the presentation of antigens to the adaptive immune system. The MHC also influences the odour-based choice of mates in humans and several animal taxa. It has recently been shown that female three-spined sticklebacks (Gasterosteus aculeatus) aim at a moderately high MHC diversity in their offspring when choosing a mate. Do they optimize the immune systems of their offspring? Using three-spined sticklebacks that varied in their individual numbers of MHC class IIB molecules, we tested, experimentally, whether allelic diversity at the MHC influences parasite resistance and immune parameters. We found that sticklebacks with low MHC diversity suffered more from parasite infection after experimental exposure to Schistocephalus solidus tapeworms and Glugea anomala microsporidians. They also showed the highest proportion of granulocytes and the strongest respiratory burst reaction, which are correlates of innate immunity. This indicates a strong activity of the innate immune system after challenge by parasites when MHC diversity is suboptimal. Individuals with very high allelic diversity at the MHC seemed inferior to those with moderately high diversity. Such a pattern is consistent with theoretical expectations of an optimal balance between the number of recognizable antigens and self-tolerance.

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Year:  2004        PMID: 15058398      PMCID: PMC1691569          DOI: 10.1098/rspb.2003.2567

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  24 in total

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  66 in total

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4.  MHC genes and oxidative stress in sticklebacks: an immuno-ecological approach.

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8.  Mate choice decisions of stickleback females predictably modified by MHC peptide ligands.

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