Sympatric and allopatric divergence of MHC genes in threespine stickleback.

Parasites can strongly affect the evolution of their hosts, but their effects on host diversification are less clear. In theory, contrasting parasite communities in different foraging habitats could generate divergent selection on hosts and promote ecological speciation. Immune systems are costly to...

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Main Authors: Blake Matthews, Luke J Harmon, Leithen M'Gonigle, Kerry B Marchinko, Helmut Schaschl
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-06-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2886830?pdf=render
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spelling doaj-6969a8c3fb284e58a2578d234a78c5452020-11-25T01:57:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-06-0156e1094810.1371/journal.pone.0010948Sympatric and allopatric divergence of MHC genes in threespine stickleback.Blake MatthewsLuke J HarmonLeithen M'GonigleKerry B MarchinkoHelmut SchaschlParasites can strongly affect the evolution of their hosts, but their effects on host diversification are less clear. In theory, contrasting parasite communities in different foraging habitats could generate divergent selection on hosts and promote ecological speciation. Immune systems are costly to maintain, adaptable, and an important component of individual fitness. As a result, immune system genes, such as those of the Major Histocompatibility Complex (MHC), can change rapidly in response to parasite-mediated selection. In threespine stickleback (Gasterosteus aculeatus), as well as in other vertebrates, MHC genes have been linked with female mating preference, suggesting that divergent selection acting on MHC genes might influence speciation. Here, we examined genetic variation at MHC Class II loci of sticklebacks from two lakes with a limnetic and benthic species pair, and two lakes with a single species. In both lakes with species pairs, limnetics and benthics differed in their composition of MHC alleles, and limnetics had fewer MHC alleles per individual than benthics. Similar to the limnetics, the allopatric population with a pelagic phenotype had few MHC alleles per individual, suggesting a correlation between MHC genotype and foraging habitat. Using a simulation model we show that the diversity and composition of MHC alleles in a sympatric species pair depends on the amount of assortative mating and on the strength of parasite-mediated selection in adjacent foraging habitats. Our results indicate parallel divergence in the number of MHC alleles between sympatric stickleback species, possibly resulting from the contrasting parasite communities in littoral and pelagic habitats of lakes.http://europepmc.org/articles/PMC2886830?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Blake Matthews
Luke J Harmon
Leithen M'Gonigle
Kerry B Marchinko
Helmut Schaschl
spellingShingle Blake Matthews
Luke J Harmon
Leithen M'Gonigle
Kerry B Marchinko
Helmut Schaschl
Sympatric and allopatric divergence of MHC genes in threespine stickleback.
PLoS ONE
author_facet Blake Matthews
Luke J Harmon
Leithen M'Gonigle
Kerry B Marchinko
Helmut Schaschl
author_sort Blake Matthews
title Sympatric and allopatric divergence of MHC genes in threespine stickleback.
title_short Sympatric and allopatric divergence of MHC genes in threespine stickleback.
title_full Sympatric and allopatric divergence of MHC genes in threespine stickleback.
title_fullStr Sympatric and allopatric divergence of MHC genes in threespine stickleback.
title_full_unstemmed Sympatric and allopatric divergence of MHC genes in threespine stickleback.
title_sort sympatric and allopatric divergence of mhc genes in threespine stickleback.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-06-01
description Parasites can strongly affect the evolution of their hosts, but their effects on host diversification are less clear. In theory, contrasting parasite communities in different foraging habitats could generate divergent selection on hosts and promote ecological speciation. Immune systems are costly to maintain, adaptable, and an important component of individual fitness. As a result, immune system genes, such as those of the Major Histocompatibility Complex (MHC), can change rapidly in response to parasite-mediated selection. In threespine stickleback (Gasterosteus aculeatus), as well as in other vertebrates, MHC genes have been linked with female mating preference, suggesting that divergent selection acting on MHC genes might influence speciation. Here, we examined genetic variation at MHC Class II loci of sticklebacks from two lakes with a limnetic and benthic species pair, and two lakes with a single species. In both lakes with species pairs, limnetics and benthics differed in their composition of MHC alleles, and limnetics had fewer MHC alleles per individual than benthics. Similar to the limnetics, the allopatric population with a pelagic phenotype had few MHC alleles per individual, suggesting a correlation between MHC genotype and foraging habitat. Using a simulation model we show that the diversity and composition of MHC alleles in a sympatric species pair depends on the amount of assortative mating and on the strength of parasite-mediated selection in adjacent foraging habitats. Our results indicate parallel divergence in the number of MHC alleles between sympatric stickleback species, possibly resulting from the contrasting parasite communities in littoral and pelagic habitats of lakes.
url http://europepmc.org/articles/PMC2886830?pdf=render
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