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The evolution and maintenance of polymorphism in the major histocompatibility complex
M J Stear1, G T Innocent, J Buitkamp
1Institute of Comparative Medicine, University of Glasgow, Bearsden Road, Glasgow G61 1QH, UK. m.j.stear@vet.gla.ac.uk
Veterinary Immunology and Immunopathology
|August 16, 2005
Summary
Genetic variations in the ovine major histocompatibility complex (MHC) influence nematode resistance in lambs. Specific MHC alleles and heterozygote advantage contribute to this resistance, impacting parasite control strategies.
Area of Science:
- Immunogenetics
- Animal Science
- Parasitology
Background:
- The ovine major histocompatibility complex (MHC) plays a crucial role in immune responses.
- Previous studies indicated a link between MHC alleles and nematode resistance in sheep.
- Genetic variation within the MHC is known to influence disease resistance.
Purpose of the Study:
- To confirm the association between specific ovine MHC DRB1 alleles and nematode egg counts.
- To investigate the role of MHC variation in genetic resistance to nematode infections.
- To explore the impact of heterozygote advantage on MHC polymorphism and parasite resistance.
Main Methods:
- Analysis of faecal nematode egg counts in lambs.
- Genotyping of the ovine MHC class II DRB1 locus.
- Comparison of nematode resistance between lambs with different MHC genotypes (G2 vs. I alleles, homozygotes vs. heterozygotes).
Main Results:
- Lambs with the G2 allele at the ovine MHC DRB1 locus exhibited lower faecal nematode egg counts compared to those with the I allele.
- This association was consistently observed across separate lamb cohorts from the same farm.
- Heterozygotes for MHC alleles demonstrated increased resistance to nematodes compared to homozygotes.
Conclusions:
- Variation within the ovine MHC significantly contributes to the genetic basis of nematode resistance.
- The G2 allele at the MHC DRB1 locus is associated with enhanced nematode resistance in lambs.
- Heterozygote advantage at MHC loci is a key factor in maintaining MHC polymorphism and driving parasite resistance.