Cargando…

Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific

1. Insects are important models for studying immunity in an ecological and evolutionary context. Yet, most empirical work on the insect immune system has come from phenotypic studies meaning we have a limited understanding of the genetic architecture of immune function in the sexes. 2. We use nine h...

Descripción completa

Detalles Bibliográficos
Autores principales: Letendre, Corinne, Duffield, Kristin R., Sadd, Ben M., Sakaluk, Scott K., House, Clarissa M., Hunt, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545791/
https://www.ncbi.nlm.nih.gov/pubmed/35470433
http://dx.doi.org/10.1111/1365-2656.13709
_version_ 1784804898176499712
author Letendre, Corinne
Duffield, Kristin R.
Sadd, Ben M.
Sakaluk, Scott K.
House, Clarissa M.
Hunt, John
author_facet Letendre, Corinne
Duffield, Kristin R.
Sadd, Ben M.
Sakaluk, Scott K.
House, Clarissa M.
Hunt, John
author_sort Letendre, Corinne
collection PubMed
description 1. Insects are important models for studying immunity in an ecological and evolutionary context. Yet, most empirical work on the insect immune system has come from phenotypic studies meaning we have a limited understanding of the genetic architecture of immune function in the sexes. 2. We use nine highly inbred lines to thoroughly examine the genetic relationships between a suite of commonly used immune assays (haemocyte count, implant encapsulation, total phenoloxidase activity, antibacterial zone of inhibition and pathogen clearance) and resistance to infection by three generalist insect pathogens (the gram‐negative bacterium Serratia marcescens, the gram‐positive bacterium Bacillus cereus and the fungus Metarhizium robertsii) in male and female Gryllodes sigillatus. 3. There were consistent positive genetic correlations between haemocyte count, antibacterial and phenoloxidase activity and resistance to S. marcescens in both sexes, but these relationships were less consistent for resistance to B. cereus and M. robertsii. In addition, the clearance of S. marcescens was genetically correlated with the resistance to all three pathogens in both sexes. Genetic correlations between resistances to the different pathogen species were inconsistent, indicating that resistance to one pathogen does not necessarily mean resistance to another. Finally, while there is ample genetic (co)variance in immune assays and pathogen resistance, these genetic estimates differed across the sexes and many of these measures were not genetically correlated across the sexes, suggesting that these measures could evolve independently in the sexes. 4. Our finding that the genetic architecture of immune function is sex and pathogen specific suggests that the evolution of immune function in male and female G. sigillatus is likely to be complex. Similar quantitative genetic studies that measure a large number of assays and resistance to multiple pathogens in both sexes are needed to ascertain if this complexity extends to other species.
format Online
Article
Text
id pubmed-9545791
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-95457912022-10-14 Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific Letendre, Corinne Duffield, Kristin R. Sadd, Ben M. Sakaluk, Scott K. House, Clarissa M. Hunt, John J Anim Ecol Research Articles 1. Insects are important models for studying immunity in an ecological and evolutionary context. Yet, most empirical work on the insect immune system has come from phenotypic studies meaning we have a limited understanding of the genetic architecture of immune function in the sexes. 2. We use nine highly inbred lines to thoroughly examine the genetic relationships between a suite of commonly used immune assays (haemocyte count, implant encapsulation, total phenoloxidase activity, antibacterial zone of inhibition and pathogen clearance) and resistance to infection by three generalist insect pathogens (the gram‐negative bacterium Serratia marcescens, the gram‐positive bacterium Bacillus cereus and the fungus Metarhizium robertsii) in male and female Gryllodes sigillatus. 3. There were consistent positive genetic correlations between haemocyte count, antibacterial and phenoloxidase activity and resistance to S. marcescens in both sexes, but these relationships were less consistent for resistance to B. cereus and M. robertsii. In addition, the clearance of S. marcescens was genetically correlated with the resistance to all three pathogens in both sexes. Genetic correlations between resistances to the different pathogen species were inconsistent, indicating that resistance to one pathogen does not necessarily mean resistance to another. Finally, while there is ample genetic (co)variance in immune assays and pathogen resistance, these genetic estimates differed across the sexes and many of these measures were not genetically correlated across the sexes, suggesting that these measures could evolve independently in the sexes. 4. Our finding that the genetic architecture of immune function is sex and pathogen specific suggests that the evolution of immune function in male and female G. sigillatus is likely to be complex. Similar quantitative genetic studies that measure a large number of assays and resistance to multiple pathogens in both sexes are needed to ascertain if this complexity extends to other species. John Wiley and Sons Inc. 2022-05-03 2022-07 /pmc/articles/PMC9545791/ /pubmed/35470433 http://dx.doi.org/10.1111/1365-2656.13709 Text en © 2022 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. 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 Research Articles
Letendre, Corinne
Duffield, Kristin R.
Sadd, Ben M.
Sakaluk, Scott K.
House, Clarissa M.
Hunt, John
Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title_full Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title_fullStr Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title_full_unstemmed Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title_short Genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
title_sort genetic covariance in immune measures and pathogen resistance in decorated crickets is sex and pathogen specific
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545791/
https://www.ncbi.nlm.nih.gov/pubmed/35470433
http://dx.doi.org/10.1111/1365-2656.13709
work_keys_str_mv AT letendrecorinne geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific
AT duffieldkristinr geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific
AT saddbenm geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific
AT sakalukscottk geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific
AT houseclarissam geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific
AT huntjohn geneticcovarianceinimmunemeasuresandpathogenresistanceindecoratedcricketsissexandpathogenspecific