4.6 Article

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

Journal

JOURNAL OF ANIMAL ECOLOGY
Volume 91, Issue 7, Pages 1471-1488

Publisher

WILEY
DOI: 10.1111/1365-2656.13709

Keywords

disease resistance; ecological immunity; immune assay; insect; pathogen; sexual dimorphism

Funding

  1. Agricultural Research Service
  2. Australian Research Council [DP180101708]
  3. Fonds de Recherche du Quebec -Nature et Technologies
  4. National Science Foundation [IOS 16-54028]
  5. Western Sydney University

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This study investigates the genetic architecture of the immune system in insects using Gryllodes sigillatus as a model. The results show that there are genetic correlations between haemocyte count, antibacterial and phenoloxidase activity, and resistance to a specific bacterium in both males and females. The ability to clear bacteria is also genetically correlated with resistance to all three pathogens. However, genetic correlations between resistances to different pathogens are inconsistent, indicating that resistance to one pathogen does not necessarily confer resistance to another. Genetic estimates of immune assays and pathogen resistance differ across sexes, suggesting independent evolution of these measures in males and females.
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. 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. 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. 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.

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