Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783660917803712512 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7934958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT heshulin evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT sieksmeyerthorben evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT cheyanli evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT moramalejandraesparza evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT stiblikpetr evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT banasiakronald evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT harrisonmarkc evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT sobotnikjan evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT wangzongqing evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT johnstonpaulr evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites AT mcmahondinop evidenceforreducedimmunegenediversityandactivityduringtheevolutionoftermites |