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Macroevolutionary foundations of a recently evolved innate immune defense

Antagonistic interactions between hosts and parasites may drive the evolution of novel host defenses, or new parasite strategies. Host immunity is therefore one of the fastest evolving traits. But where do the novel immune traits come from? Here, we test for phylogenetic conservation in a rapidly ev...

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Autores principales: Vrtílek, Milan, Bolnick, Daniel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488947/
https://www.ncbi.nlm.nih.gov/pubmed/34347301
http://dx.doi.org/10.1111/evo.14316
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author Vrtílek, Milan
Bolnick, Daniel I.
author_facet Vrtílek, Milan
Bolnick, Daniel I.
author_sort Vrtílek, Milan
collection PubMed
description Antagonistic interactions between hosts and parasites may drive the evolution of novel host defenses, or new parasite strategies. Host immunity is therefore one of the fastest evolving traits. But where do the novel immune traits come from? Here, we test for phylogenetic conservation in a rapidly evolving immune trait—peritoneal fibrosis. Peritoneal fibrosis is a costly defense against a specialist tapeworm, Schistocephalus solidus (Cestoda), expressed in some freshwater populations of threespine stickleback fish (Gasterosteus aculeatus, Perciformes). We asked whether stickleback fibrosis is a derived species‐specific trait or an ancestral immune response that was widely distributed across ray‐finned fish (Actinopterygii) only to be employed by threespine stickleback against the specialist parasite. We combined literature review on peritoneal fibrosis with a comparative experiment using either parasite‐specific, or nonspecific, immune challenge in deliberately selected species across fish tree of life. We show that ray‐finned fish are broadly, but not universally, able to induce peritoneal fibrosis when challenged with a generic stimulus (Alum adjuvant). The experimental species were, however, largely indifferent to the tapeworm antigen homogenate. Peritoneal fibrosis, thus, appears to be a common and deeply conserved fish immune response that was co‐opted by stickleback to adapt to a new selective challenge.
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spelling pubmed-84889472022-10-01 Macroevolutionary foundations of a recently evolved innate immune defense Vrtílek, Milan Bolnick, Daniel I. Evolution Brief Communications Antagonistic interactions between hosts and parasites may drive the evolution of novel host defenses, or new parasite strategies. Host immunity is therefore one of the fastest evolving traits. But where do the novel immune traits come from? Here, we test for phylogenetic conservation in a rapidly evolving immune trait—peritoneal fibrosis. Peritoneal fibrosis is a costly defense against a specialist tapeworm, Schistocephalus solidus (Cestoda), expressed in some freshwater populations of threespine stickleback fish (Gasterosteus aculeatus, Perciformes). We asked whether stickleback fibrosis is a derived species‐specific trait or an ancestral immune response that was widely distributed across ray‐finned fish (Actinopterygii) only to be employed by threespine stickleback against the specialist parasite. We combined literature review on peritoneal fibrosis with a comparative experiment using either parasite‐specific, or nonspecific, immune challenge in deliberately selected species across fish tree of life. We show that ray‐finned fish are broadly, but not universally, able to induce peritoneal fibrosis when challenged with a generic stimulus (Alum adjuvant). The experimental species were, however, largely indifferent to the tapeworm antigen homogenate. Peritoneal fibrosis, thus, appears to be a common and deeply conserved fish immune response that was co‐opted by stickleback to adapt to a new selective challenge. John Wiley and Sons Inc. 2021-08-15 2021-10 /pmc/articles/PMC8488947/ /pubmed/34347301 http://dx.doi.org/10.1111/evo.14316 Text en © 2021 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Brief Communications
Vrtílek, Milan
Bolnick, Daniel I.
Macroevolutionary foundations of a recently evolved innate immune defense
title Macroevolutionary foundations of a recently evolved innate immune defense
title_full Macroevolutionary foundations of a recently evolved innate immune defense
title_fullStr Macroevolutionary foundations of a recently evolved innate immune defense
title_full_unstemmed Macroevolutionary foundations of a recently evolved innate immune defense
title_short Macroevolutionary foundations of a recently evolved innate immune defense
title_sort macroevolutionary foundations of a recently evolved innate immune defense
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8488947/
https://www.ncbi.nlm.nih.gov/pubmed/34347301
http://dx.doi.org/10.1111/evo.14316
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