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Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq

Host–pathogen associations change rapidly during a biological invasion and are predicted to impose strong selection on immune function. It has been proposed that the invader may experience an abrupt reduction in pathogen‐mediated selection (“enemy release”), thereby favoring decreased investment int...

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Autores principales: Selechnik, Daniel, Richardson, Mark F., Shine, Richard, Brown, Gregory P., Rollins, Lee Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580278/
https://www.ncbi.nlm.nih.gov/pubmed/31236254
http://dx.doi.org/10.1002/ece3.5249
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author Selechnik, Daniel
Richardson, Mark F.
Shine, Richard
Brown, Gregory P.
Rollins, Lee Ann
author_facet Selechnik, Daniel
Richardson, Mark F.
Shine, Richard
Brown, Gregory P.
Rollins, Lee Ann
author_sort Selechnik, Daniel
collection PubMed
description Host–pathogen associations change rapidly during a biological invasion and are predicted to impose strong selection on immune function. It has been proposed that the invader may experience an abrupt reduction in pathogen‐mediated selection (“enemy release”), thereby favoring decreased investment into “costly” immune responses. Across plants and animals, there is mixed support for this prediction. Pathogens are not the only form of selection imposed on invaders; differences in abiotic environmental conditions between native and introduced ranges are also expected to drive rapid evolution. Here, we use RNA‐Seq to assess the expression patterns of immune and environmentally associated genes in the cane toad (Rhinella marina) across its invasive Australian range. Transcripts encoding mediators of costly immune responses (inflammation, cytotoxicity) showed a curvilinear relationship with invasion history, with highest expression in toads from oldest and newest colonized areas. This pattern is surprising given theoretical expectations of density dynamics in invasive species and may be because density influences both intraspecific competition and parasite transmission, generating conflicting effects on the strength of immune responses. Alternatively, this expression pattern may be the result of other evolutionary forces, such as spatial sorting and genetic drift, working simultaneously with natural selection. Our findings do not support predictions about immune function based on the enemy release hypothesis and suggest instead that the effects of enemy release are difficult to isolate in wild populations, especially in the absence of information regarding parasite and pathogen infection. Additionally, expression patterns of genes underlying putatively environmentally associated traits are consistent with previous genetic studies, providing further support that Australian cane toads have adapted to novel abiotic challenges.
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spelling pubmed-65802782019-06-24 Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq Selechnik, Daniel Richardson, Mark F. Shine, Richard Brown, Gregory P. Rollins, Lee Ann Ecol Evol Original Research Host–pathogen associations change rapidly during a biological invasion and are predicted to impose strong selection on immune function. It has been proposed that the invader may experience an abrupt reduction in pathogen‐mediated selection (“enemy release”), thereby favoring decreased investment into “costly” immune responses. Across plants and animals, there is mixed support for this prediction. Pathogens are not the only form of selection imposed on invaders; differences in abiotic environmental conditions between native and introduced ranges are also expected to drive rapid evolution. Here, we use RNA‐Seq to assess the expression patterns of immune and environmentally associated genes in the cane toad (Rhinella marina) across its invasive Australian range. Transcripts encoding mediators of costly immune responses (inflammation, cytotoxicity) showed a curvilinear relationship with invasion history, with highest expression in toads from oldest and newest colonized areas. This pattern is surprising given theoretical expectations of density dynamics in invasive species and may be because density influences both intraspecific competition and parasite transmission, generating conflicting effects on the strength of immune responses. Alternatively, this expression pattern may be the result of other evolutionary forces, such as spatial sorting and genetic drift, working simultaneously with natural selection. Our findings do not support predictions about immune function based on the enemy release hypothesis and suggest instead that the effects of enemy release are difficult to isolate in wild populations, especially in the absence of information regarding parasite and pathogen infection. Additionally, expression patterns of genes underlying putatively environmentally associated traits are consistent with previous genetic studies, providing further support that Australian cane toads have adapted to novel abiotic challenges. John Wiley and Sons Inc. 2019-05-09 /pmc/articles/PMC6580278/ /pubmed/31236254 http://dx.doi.org/10.1002/ece3.5249 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Selechnik, Daniel
Richardson, Mark F.
Shine, Richard
Brown, Gregory P.
Rollins, Lee Ann
Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title_full Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title_fullStr Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title_full_unstemmed Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title_short Immune and environment‐driven gene expression during invasion: An eco‐immunological application of RNA‐Seq
title_sort immune and environment‐driven gene expression during invasion: an eco‐immunological application of rna‐seq
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580278/
https://www.ncbi.nlm.nih.gov/pubmed/31236254
http://dx.doi.org/10.1002/ece3.5249
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