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Evidence for reduced immune gene diversity and activity during the evolution of termites

The evolution of biological complexity is associated with the emergence of bespoke immune systems that maintain and protect organism integrity. Unlike the well-studied immune systems of cells and individuals, little is known about the origins of immunity during the transition to eusociality, a major...

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Autores principales: He, Shulin, Sieksmeyer, Thorben, Che, Yanli, Mora, M. Alejandra Esparza, Stiblik, Petr, Banasiak, Ronald, Harrison, Mark C., Šobotník, Jan, Wang, Zongqing, Johnston, Paul R., McMahon, Dino P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934958/
https://www.ncbi.nlm.nih.gov/pubmed/33593190
http://dx.doi.org/10.1098/rspb.2020.3168
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author He, Shulin
Sieksmeyer, Thorben
Che, Yanli
Mora, M. Alejandra Esparza
Stiblik, Petr
Banasiak, Ronald
Harrison, Mark C.
Šobotník, Jan
Wang, Zongqing
Johnston, Paul R.
McMahon, Dino P.
author_facet He, Shulin
Sieksmeyer, Thorben
Che, Yanli
Mora, M. Alejandra Esparza
Stiblik, Petr
Banasiak, Ronald
Harrison, Mark C.
Šobotník, Jan
Wang, Zongqing
Johnston, Paul R.
McMahon, Dino P.
author_sort He, Shulin
collection PubMed
description The evolution of biological complexity is associated with the emergence of bespoke immune systems that maintain and protect organism integrity. Unlike the well-studied immune systems of cells and individuals, little is known about the origins of immunity during the transition to eusociality, a major evolutionary transition comparable to the evolution of multicellular organisms from single-celled ancestors. We aimed to tackle this by characterizing the immune gene repertoire of 18 cockroach and termite species, spanning the spectrum of solitary, subsocial and eusocial lifestyles. We find that key transitions in termite sociality are correlated with immune gene family contractions. In cross-species comparisons of immune gene expression, we find evidence for a caste-specific social defence system in termites, which appears to operate at the expense of individual immune protection. Our study indicates that a major transition in organismal complexity may have entailed a fundamental reshaping of the immune system optimized for group over individual defence.
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spelling pubmed-79349582021-04-10 Evidence for reduced immune gene diversity and activity during the evolution of termites He, Shulin Sieksmeyer, Thorben Che, Yanli Mora, M. Alejandra Esparza Stiblik, Petr Banasiak, Ronald Harrison, Mark C. Šobotník, Jan Wang, Zongqing Johnston, Paul R. McMahon, Dino P. Proc Biol Sci Evolution The evolution of biological complexity is associated with the emergence of bespoke immune systems that maintain and protect organism integrity. Unlike the well-studied immune systems of cells and individuals, little is known about the origins of immunity during the transition to eusociality, a major evolutionary transition comparable to the evolution of multicellular organisms from single-celled ancestors. We aimed to tackle this by characterizing the immune gene repertoire of 18 cockroach and termite species, spanning the spectrum of solitary, subsocial and eusocial lifestyles. We find that key transitions in termite sociality are correlated with immune gene family contractions. In cross-species comparisons of immune gene expression, we find evidence for a caste-specific social defence system in termites, which appears to operate at the expense of individual immune protection. Our study indicates that a major transition in organismal complexity may have entailed a fundamental reshaping of the immune system optimized for group over individual defence. The Royal Society 2021-02-24 2021-02-17 /pmc/articles/PMC7934958/ /pubmed/33593190 http://dx.doi.org/10.1098/rspb.2020.3168 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
He, Shulin
Sieksmeyer, Thorben
Che, Yanli
Mora, M. Alejandra Esparza
Stiblik, Petr
Banasiak, Ronald
Harrison, Mark C.
Šobotník, Jan
Wang, Zongqing
Johnston, Paul R.
McMahon, Dino P.
Evidence for reduced immune gene diversity and activity during the evolution of termites
title Evidence for reduced immune gene diversity and activity during the evolution of termites
title_full Evidence for reduced immune gene diversity and activity during the evolution of termites
title_fullStr Evidence for reduced immune gene diversity and activity during the evolution of termites
title_full_unstemmed Evidence for reduced immune gene diversity and activity during the evolution of termites
title_short Evidence for reduced immune gene diversity and activity during the evolution of termites
title_sort evidence for reduced immune gene diversity and activity during the evolution of termites
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934958/
https://www.ncbi.nlm.nih.gov/pubmed/33593190
http://dx.doi.org/10.1098/rspb.2020.3168
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