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Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System
Heritable population differences in immune gene expression following infection can reveal mechanisms of host immune evolution. We compared gene expression in infected and uninfected threespine stickleback (Gasterosteus aculeatus) from two natural populations that differ in resistance to a native ces...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600903/ https://www.ncbi.nlm.nih.gov/pubmed/28955327 http://dx.doi.org/10.3389/fimmu.2017.01071 |
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author | Lohman, Brian K. Steinel, Natalie C. Weber, Jesse N. Bolnick, Daniel I. |
author_facet | Lohman, Brian K. Steinel, Natalie C. Weber, Jesse N. Bolnick, Daniel I. |
author_sort | Lohman, Brian K. |
collection | PubMed |
description | Heritable population differences in immune gene expression following infection can reveal mechanisms of host immune evolution. We compared gene expression in infected and uninfected threespine stickleback (Gasterosteus aculeatus) from two natural populations that differ in resistance to a native cestode parasite, Schistocephalus solidus. Genes in both the innate and adaptive immune system were differentially expressed as a function of host population, infection status, and their interaction. These genes were enriched for loci controlling immune functions known to differ between host populations or in response to infection. Coexpression network analysis identified two distinct processes contributing to resistance: parasite survival and suppression of growth. Comparing networks between populations showed resistant fish have a dynamic expression profile while susceptible fish are static. In summary, recent evolutionary divergence between two vertebrate populations has generated population-specific gene expression responses to parasite infection, affecting parasite establishment and growth. |
format | Online Article Text |
id | pubmed-5600903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56009032017-09-27 Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System Lohman, Brian K. Steinel, Natalie C. Weber, Jesse N. Bolnick, Daniel I. Front Immunol Immunology Heritable population differences in immune gene expression following infection can reveal mechanisms of host immune evolution. We compared gene expression in infected and uninfected threespine stickleback (Gasterosteus aculeatus) from two natural populations that differ in resistance to a native cestode parasite, Schistocephalus solidus. Genes in both the innate and adaptive immune system were differentially expressed as a function of host population, infection status, and their interaction. These genes were enriched for loci controlling immune functions known to differ between host populations or in response to infection. Coexpression network analysis identified two distinct processes contributing to resistance: parasite survival and suppression of growth. Comparing networks between populations showed resistant fish have a dynamic expression profile while susceptible fish are static. In summary, recent evolutionary divergence between two vertebrate populations has generated population-specific gene expression responses to parasite infection, affecting parasite establishment and growth. Frontiers Media S.A. 2017-09-12 /pmc/articles/PMC5600903/ /pubmed/28955327 http://dx.doi.org/10.3389/fimmu.2017.01071 Text en Copyright © 2017 Lohman, Steinel, Weber and Bolnick. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Lohman, Brian K. Steinel, Natalie C. Weber, Jesse N. Bolnick, Daniel I. Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title | Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title_full | Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title_fullStr | Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title_full_unstemmed | Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title_short | Gene Expression Contributes to the Recent Evolution of Host Resistance in a Model Host Parasite System |
title_sort | gene expression contributes to the recent evolution of host resistance in a model host parasite system |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600903/ https://www.ncbi.nlm.nih.gov/pubmed/28955327 http://dx.doi.org/10.3389/fimmu.2017.01071 |
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