Evidence map›Paper›PMID 39491325›Full record

ArticleMolecular ecology2024

Conserved and Unique Protein Expression Patterns Across Reproductive Stage Transitions in Social Hymenopteran Queens.

Alison McAfee, Baptiste Martinet, Kimberly Przybyla, Félicien Degueldre, Shelley E Hoover, Serge Aron, Leonard J Foster

Abstract read
In one paragraph

Article in Molecular ecology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Elevated virus infection of honey bee queens reduces methyl oleate production and destabilizes colony-level social structure.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
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

7 authors.

Alison McAfeeDepartment of Biochemistry and Molecular Biology, Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0003-3523-6649
Baptiste MartinetDepartment of Evolutionary Biology & Ecology, Université Libre de Bruxelles, Brussels, Belgium.
Kimberly PrzybylaDepartment of Zoology, University of Mons, Mons, Belgium.
Félicien DegueldreDepartment of Evolutionary Biology & Ecology, Université Libre de Bruxelles, Brussels, Belgium.
Shelley E HooverDepartment of Biological Sciences, University of Lethbridge, Lethbridge, Alberta, Canada.
Serge AronDepartment of Evolutionary Biology & Ecology, Université Libre de Bruxelles, Brussels, Belgium.
Leonard J FosterDepartment of Biochemistry and Molecular Biology, Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

BC Knowledge Development FundCanada Foundation for InnovationCenter for Blood ResearchFonds De La Recherche Scientifique - FNRS J.0008.23Genome British Columbia 374PROL'Oreal-UNESCOResults-Driven Agricultural ResearchUBC Life Sciences InstituteUniversité Libre de Bruxelles
6 · The paper itself

Abstract

Hymenopteran queens are collectively highly fecund, often long-lived individuals that undergo dramatic physiological changes after they mate and establish a nest. However, the degree to which these changes are conserved among species with different life histories is not well-defined. We conducted a comparative proteomic study investigating differences between reproductive stages (virgin, mated and established queens) of Apis mellifera, Bombus impatiens, B. terrestris and Lasius niger. We analysed haemolymph for all species except L. niger, for which a whole-body analysis was performed due to the small size of these queens. We identified conserved upregulation of proteins involved in anatomical and system development as queens transition to establishing a nest in all species except B. terrestris. We also identified conserved patterns of vitellogenin, vitellogenin receptor and immune-responsive protein (IRP)30, all of which are proteins typically associated with oviposition. However, expression patterns of other immune proteins, heat-shock proteins (HSPs), detoxification enzymes and antioxidant enzymes were more dissimilar, with some species exhibiting similar trends and co-occurrence through reproductive stages, while others exhibited variable or opposite patterns. These conserved and unique profiles likely in part reflect similarities and differences in selective pressure on reproductive stages of each species and may indicate differing abilities to respond to emergent pathogens or environmental change.

Indexed as

Insect ProteinsProteomicsReproductionVitellogeninsAnimalsBeesEgg ProteinsFemaleHemolymphHymenopteraOvipositionReceptors, Cell SurfaceEgg ProteinsInsect ProteinsReceptors, Cell Surfacevitellogenin receptorVitellogeninsadaptationanimal mating/breeding systemscomparative biologygenomics/proteomicsinsects

Identifiers

PMID39491325
PMCPMC11589692

What Socratic 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 Socratic graph.