Related Experiment Videos
Multiple parasites are driving major histocompatibility complex polymorphism in the wild.
K M Wegner1, T B H Reusch, M Kalbe
1Max-Planck-Institute of Limnology, Department of Evolutionary Ecology, Plön, Germany. wegner@mpil-ploen.mpg.de
Journal of Evolutionary Biology
|November 26, 2003
Summary
Parasite diversity drives the evolution of immune genes in three-spined sticklebacks. Fish with intermediate immune gene diversity had fewer parasites, suggesting an optimal strategy for disease resistance.
Area of Science:
- Evolutionary biology
- Immunogenetics
- Ecology
Background:
- Parasite-mediated selection can lead to co-evolutionary arms races between hosts and parasites.
- Simultaneous infections may promote genetic diversity in host resistance genes at population and individual levels.
Purpose of the Study:
- To investigate the influence of parasite diversity on the evolution of Major Histocompatibility Complex (MHC) genes in three-spined sticklebacks.
- To determine if MHC diversity correlates with parasite load within individual fish.
Main Methods:
- Analysis of MHC class IIB gene diversity in eight natural populations of three-spined sticklebacks.
- Assessment of parasite diversity and abundance across different habitat types (lakes, rivers, estuaries).
- Correlation analysis between MHC diversity, parasite diversity, and general genetic diversity (microsatellites).
Main Results:
- MHC class IIB and parasite diversity varied significantly across habitats, with lowest diversity in rivers.
- Parasite diversity positively influenced MHC class IIB variation, while general genetic diversity did not.
- Individual fish with intermediate MHC allele numbers exhibited lower parasite loads.
Conclusions:
- Parasite pressure contributes to the diversification of immune genes in natural populations.
- Intermediate MHC diversity is associated with optimal immunocompetence, supporting an 'allele counting' strategy.
- Mate choice in female sticklebacks may favor partners that enhance offspring immunocompetence through MHC diversity.