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Between-population differences in constitutive and infection-induced gene expression in threespine stickleback

Fuess, Lauren E. ; Weber, Jesse N. ; den Haan, Stijn ; Steinel, Natalie C. ; Shim, Kum Chuan and Bolnick, Daniel I. (2021) In Molecular Ecology 30(24). p.6791-6805
Abstract

Vertebrate immunity is a complex system consisting of a mix of constitutive and inducible defences. Furthermore, host immunity is subject to selective pressure from a range of parasites and pathogens which can produce variation in these defences across populations. As populations evolve immune responses to parasites, they may adapt via a combination of (1) constitutive differences, (2) shared inducible responses, or (3) divergent inducible responses. Here, we leverage a powerful natural host-parasite model system (Gasterosteus aculeatus and Schistochephalus solidus) to tease apart the relative contributions of these three types of adaptations to among-population divergence in response to parasites. Gene expression analyses revealed... (More)

Vertebrate immunity is a complex system consisting of a mix of constitutive and inducible defences. Furthermore, host immunity is subject to selective pressure from a range of parasites and pathogens which can produce variation in these defences across populations. As populations evolve immune responses to parasites, they may adapt via a combination of (1) constitutive differences, (2) shared inducible responses, or (3) divergent inducible responses. Here, we leverage a powerful natural host-parasite model system (Gasterosteus aculeatus and Schistochephalus solidus) to tease apart the relative contributions of these three types of adaptations to among-population divergence in response to parasites. Gene expression analyses revealed limited evidence of significant divergence in constitutive expression of immune defence, and strong signatures of conserved inducible responses to the parasite. Furthermore, our results highlight a handful of immune-related genes which show divergent inducible responses which may contribute disproportionately to functional differences in infection success or failure. In addition to investigating variation in evolutionary adaptation to parasite selection, we also leverage this unique data set to improve understanding of cellular mechanisms underlying a putative resistance phenotype (fibrosis). Combined, our results provide a case study in evolutionary immunology showing that a very small number of genes may contribute to genotype differences in infection response.

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author
; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
subject
keywords
ecoimmunology, evolutionary immunology, fibrosis, host-parasite interactions
in
Molecular Ecology
volume
30
issue
24
pages
6791 - 6805
publisher
Wiley-Blackwell
external identifiers
  • scopus:85117107683
  • pmid:34582586
ISSN
0962-1083
DOI
10.1111/mec.16197
language
English
LU publication?
no
additional info
Publisher Copyright: © 2021 The Authors. Molecular Ecology published by John Wiley & Sons Ltd.
id
397abdd1-0d8f-4299-8772-a8c02849936a
date added to LUP
2021-11-12 11:42:50
date last changed
2024-09-22 05:07:15
@article{397abdd1-0d8f-4299-8772-a8c02849936a,
  abstract     = {{<p>Vertebrate immunity is a complex system consisting of a mix of constitutive and inducible defences. Furthermore, host immunity is subject to selective pressure from a range of parasites and pathogens which can produce variation in these defences across populations. As populations evolve immune responses to parasites, they may adapt via a combination of (1) constitutive differences, (2) shared inducible responses, or (3) divergent inducible responses. Here, we leverage a powerful natural host-parasite model system (Gasterosteus aculeatus and Schistochephalus solidus) to tease apart the relative contributions of these three types of adaptations to among-population divergence in response to parasites. Gene expression analyses revealed limited evidence of significant divergence in constitutive expression of immune defence, and strong signatures of conserved inducible responses to the parasite. Furthermore, our results highlight a handful of immune-related genes which show divergent inducible responses which may contribute disproportionately to functional differences in infection success or failure. In addition to investigating variation in evolutionary adaptation to parasite selection, we also leverage this unique data set to improve understanding of cellular mechanisms underlying a putative resistance phenotype (fibrosis). Combined, our results provide a case study in evolutionary immunology showing that a very small number of genes may contribute to genotype differences in infection response.</p>}},
  author       = {{Fuess, Lauren E. and Weber, Jesse N. and den Haan, Stijn and Steinel, Natalie C. and Shim, Kum Chuan and Bolnick, Daniel I.}},
  issn         = {{0962-1083}},
  keywords     = {{ecoimmunology; evolutionary immunology; fibrosis; host-parasite interactions}},
  language     = {{eng}},
  month        = {{09}},
  number       = {{24}},
  pages        = {{6791--6805}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{Molecular Ecology}},
  title        = {{Between-population differences in constitutive and infection-induced gene expression in threespine stickleback}},
  url          = {{http://dx.doi.org/10.1111/mec.16197}},
  doi          = {{10.1111/mec.16197}},
  volume       = {{30}},
  year         = {{2021}},
}