Evidence map›Paper›PMID 33593190›Full record

ArticleProceedings. Biological sciences2021

Evidence for reduced immune gene diversity and activity during the evolution of termites.

Shulin He, Thorben Sieksmeyer, Yanli Che, M Alejandra Esparza Mora, Petr Stiblik, Ronald Banasiak, Mark C Harrison, Jan Šobotník, Zongqing Wang, Paul R Johnston and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  5. Pervasive relaxed selection in termite genomes.Proceedings. Biological sciences · 2024
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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

11 authors at 5 institutions in 3 countries.

Shulin HeInstitute of Biology, Freie Universität Berlin, Schwendenerstr. 1, 14195 Berlin, Germany.
Thorben SieksmeyerInstitute of Biology, Freie Universität Berlin, Schwendenerstr. 1, 14195 Berlin, Germany.
Yanli CheCollege of Plant Protection, Southwest University, Tiansheng 2, 400715 Chongqing, People's Republic of China.
M Alejandra Esparza MoraInstitute of Biology, Freie Universität Berlin, Schwendenerstr. 1, 14195 Berlin, Germany.
Petr StiblikFaculty of Forestry and Wood Science, Czech University of Life Science Prague, Kamýcká 129, 16500 Prague, Czech Republic.
Ronald BanasiakDepartment for Materials and Environment, BAM Federal Institute for Materials Research and Testing, Unter den Eichen 87, 12205 Berlin, Germany.
Mark C HarrisonInstitute for Evolution and Biodiversity, University of Münster, Münster, Germany.
Jan ŠobotníkFaculty of Tropical AgriSciences, Czech University of Life Science Prague, Kamýcká 129, 16500 Prague, Czech Republic.
Zongqing WangCollege of Plant Protection, Southwest University, Tiansheng 2, 400715 Chongqing, People's Republic of China.
Paul R JohnstonInstitute of Biology, Freie Universität Berlin, Schwendenerstr. 1, 14195 Berlin, Germany.
Dino P McMahonInstitute of Biology, Freie Universität Berlin, Schwendenerstr. 1, 14195 Berlin, Germany.
Federal Institute For Materials Research and Testing · DECzech University of Life Sciences Prague · CZSouthwest University · CNLeibniz Institute of Freshwater Ecology and Inland Fisheries · DEUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The evolution of biological complexity is associated with the emergence of bespoke immune systems that maintain and protect organism integrity. Unlike the well-studied immune systems of cells and individuals, little is known about the origins of immunity during the transition to eusociality, a major evolutionary transition comparable to the evolution of multicellular organisms from single-celled ancestors. We aimed to tackle this by characterizing the immune gene repertoire of 18 cockroach and termite species, spanning the spectrum of solitary, subsocial and eusocial lifestyles. We find that key transitions in termite sociality are correlated with immune gene family contractions. In cross-species comparisons of immune gene expression, we find evidence for a caste-specific social defence system in termites, which appears to operate at the expense of individual immune protection. Our study indicates that a major transition in organismal complexity may have entailed a fundamental reshaping of the immune system optimized for group over individual defence.

Indexed as

CockroachesIsopteraAnimalsBiological EvolutionPhylogenySocial Behaviorcockroachcontractionexpansionmajor transitionsocial insectsubsocial

Identifiers

PMID33593190
PMCPMC7934958
OpenAlexW3131890167

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.