Evidence map›Paper›PMID 35470433›Full record

ArticleThe Journal of animal ecology2022

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

Corinne Letendre, Kristin R Duffield, Ben M Sadd, Scott K Sakaluk, Clarissa M House, John Hunt

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of animal ecology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Corinne LetendreSchool of Science, Western Sydney University, Richmond, NSW, Australia.ORCID 0000-0002-6457-1465
Kristin R DuffieldSchool of Biological Sciences, Illinois State University, Normal, IL, USA.
Ben M SaddSchool of Biological Sciences, Illinois State University, Normal, IL, USA.
Scott K SakalukSchool of Biological Sciences, Illinois State University, Normal, IL, USA.ORCID 0000-0003-2878-1438
Clarissa M HouseSchool of Science, Western Sydney University, Richmond, NSW, Australia.ORCID 0000-0003-1125-6354
John HuntSchool of Science, Western Sydney University, Richmond, NSW, Australia.ORCID 0000-0002-4962-8750
Illinois State University · USWestern Sydney University · AUNational Center for Agricultural Utilization Research · USUniversity of Exeter · GB

Funding

Agricultural Research ServiceAustralian Research Council DP180101708Fonds de Recherche du Québec - Nature et TechnologiesNational Science Foundation IOS 16-54028Western Sydney University
6 · The paper itself

Abstract

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.

Indexed as

GryllidaeAnimalsAnti-Bacterial AgentsFemaleGram-Negative BacteriaGram-Positive BacteriaMaleMonophenol MonooxygenaseAnti-Bacterial AgentsMonophenol Monooxygenasedisease resistanceecological immunityimmune assayinsectpathogensexual dimorphism

Identifiers

PMID35470433
PMCPMC9545791
OpenAlexW4224865653

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.