Evidence map›Paper›PMID 25908406›Full record

ArticleGenome biology2015

A depauperate immune repertoire precedes evolution of sociality in bees.

Seth M Barribeau, Ben M Sadd, Louis du Plessis, Mark J F Brown, Severine D Buechel, Kaat Cappelle, James C Carolan, Olivier Christiaens, Thomas J Colgan, Silvio Erler and 14 more

Abstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

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  18. Review
  19. Complex networks of parasites and pollinators: moving towards a healthy balance.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  20. Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Seth M BarribeauExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. barribeaus14@ecu.edu.
Ben M SaddExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. bmsadd@ilstu.edu.
Louis du PlessisTheoretical Biology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. louis.duplessis@env.ethz.ch.
Mark J F BrownSchool of Biological Sciences, Royal Holloway University of London, London, TW20 0EX, UK. mark.brown@rhul.ac.uk.
Severine D BuechelExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. severine.buechel@env.ethz.ch.
Kaat CappelleDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. kaat.cappelle@ugent.be.
James C CarolanMaynooth University Department of Biology, Maynooth University, Maynooth, Kildare, Ireland. james.carolan@nuim.ie.
Olivier ChristiaensDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. olchrist.christiaens@ugent.be.
Thomas J ColganDepartment of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin, 2, Ireland. tcolgan@tcd.ie.
Silvio ErlerDepartment of Apiculture and Sericulture, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, 400372, Romania. silvio.erler@zoologie.uni-halle.de.
Jay EvansUSDA-ARS Bee Research Laboratory, Beltsville, MD, 20705, USA. jay.evans@ars.usda.gov.
Sophie HelbingInstitut für Biologie, Molekulare Ökologie, Martin-Luther-Universität Halle-Wittenberg, Wittenberg, 06120, Germany. sophie.helbing@zoologie.uni-halle.de.
Elke KarausExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. elke.karaus@env.ethz.ch.
H Michael G LattorffInstitut für Biologie, Molekulare Ökologie, Martin-Luther-Universität Halle-Wittenberg, Wittenberg, 06120, Germany. lattorff@zoologie.uni-halle.de.
Monika MarxerExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. monika.marxer@env.ethz.ch.
Ivan MeeusDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. ivan.meeus@ugent.be.
Kathrin NäpflinExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. kathrin.naepflin@env.ethz.ch.
Jinzhi NiuDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. jinzhi.niu@ugent.be.
Regula Schmid-HempelExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. regula.schmid@env.ethz.ch.
Guy SmaggheDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. guy.smagghe@ugent.be.
Robert M WaterhouseSwiss Institute of Bioinformatics, 1211, Lausanne, Switzerland. robert.waterhouse@unige.ch.
Na YuDepartment of Crop Protection, Faculty of Bioscience Engineering, Ghent University, 9000, Ghent, Belgium. na.yu@ugent.be.
Evgeny M ZdobnovSwiss Institute of Bioinformatics, 1211, Lausanne, Switzerland. evgeny.zdobnov@unige.ch.
Paul Schmid-HempelExperimental Ecology, Institute of Integrative Biology, ETH Zürich, CH-8092, Zürich, Switzerland. paul.schmid-hempel@env.ethz.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSociality has many rewards, but can also be dangerous, as high population density and low genetic diversity, common in social insects, is ideal for parasite transmission. Despite this risk, honeybees and other sequenced social insects have far fewer canonical immune genes relative to solitary insects. Social protection from infection, including behavioral responses, may explain this depauperate immune repertoire. Here, based on full genome sequences, we describe the immune repertoire of two ecologically and commercially important bumblebee species that diverged approximately 18 million years ago, the North American Bombus impatiens and European Bombus terrestris.

resultsWe find that the immune systems of these bumblebees, two species of honeybee, and a solitary leafcutting bee, are strikingly similar. Transcriptional assays confirm the expression of many of these genes in an immunological context and more strongly in young queens than males, affirming Bateman's principle of greater investment in female immunity. We find evidence of positive selection in genes encoding antiviral responses, components of the Toll and JAK/STAT pathways, and serine protease inhibitors in both social and solitary bees. Finally, we detect many genes across pathways that differ in selection between bumblebees and honeybees, or between the social and solitary clades.

conclusionsThe similarity in immune complement across a gradient of sociality suggests that a reduced immune repertoire predates the evolution of sociality in bees. The differences in selection on immune genes likely reflect divergent pressures exerted by parasites across social contexts.

Indexed as

Behavior, AnimalEvolution, MolecularSocial BehaviorAnimalsBeesFemaleGene Expression RegulationGenes, InsectGenetic VariationMaleSelection, Genetic

Identifiers

PMID25908406
PMCPMC4408586

What OpenQuestion holds

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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.