Evidence map›Paper›PMID 35510766›Full record

ArticleMolecular ecology2022

Long term patterns of association between MHC and helminth burdens in the bank vole support Red Queen dynamics.

Magdalena Migalska, Karolina Przesmycka, Mohammed Alsarraf, Anna Bajer, Jolanta Behnke-Borowczyk, Maciej Grzybek, Jerzy M Behnke, Jacek Radwan

Open access · bronzeAbstract read
In one paragraph

Article in Molecular ecology, 2022. 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
3.9field-weighted citation impact, top 6% 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, 21 citations in OpenAlex.

  1. Article
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  5. MHC Diversity Across Time and Space.Ecology and evolution · 2025
    Review
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  7. Article
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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

8 authors at 6 institutions in 2 countries.

Magdalena MigalskaInstitute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Krakow, Poland.
Karolina PrzesmyckaInstitute of Environmental Biology, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.
Mohammed AlsarrafDepartment of Eco-epidemiology of Parasitic Diseases, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Anna BajerDepartment of Eco-epidemiology of Parasitic Diseases, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Jolanta Behnke-BorowczykDepartment of Forest Entomology and Pathology, Faculty of Forestry and Wood Technology, Poznań University of Life Sciences, Poznań, Poland.
Maciej GrzybekInstitute of Maritime and Tropical Medicine, Medical University of Gdansk, Gdynia, Poland.
Jerzy M BehnkeSchool of Life Science, University of Nottingham, Nottingham, UK.
Jacek RadwanInstitute of Environmental Biology, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland.
Adam Mickiewicz University in Poznań · PLUniversity of Warsaw · PLGdynia Maritime University · PLJagiellonian University · PLUniversity of Life Sciences in Poznań · PLUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major histocompatibility complex (MHC) genes encode proteins crucial for adaptive immunity of vertebrates. Negative frequency-dependent selection (NFDS), resulting from adaptation of parasites to common MHC types, has been hypothesized to maintain high, functionally relevant polymorphism of MHC, but demonstration of this relationship has remained elusive. In particular, differentiation of NFDS from fluctuating selection, resulting from changes in parasite communities in time and space (FS), has proved difficult in short-term studies. Here, we used temporal data, accumulated through long-term monitoring of helminths infecting bank voles (Myodes glareolus), to test specific predictions of NFDS on MHC class II. Data were collected in three, moderately genetically differentiated subpopulations in Poland, which were characterized by some stable spatiotemporal helminth communities but also events indicating introduction of new species and loss of others. We found a complex association between individual MHC diversity and species richness, where intermediate numbers of DRB supertypes correlated with lowest species richness, but the opposite was true for DQB supertypes-arguing against universal selection for immunogenetic optimality. We also showed that particular MHC supertypes explain a portion of the variance in prevalence and abundance of helminths, but this effect was subpopulation-specific, which is consistent with both NFDS and FS. Finally, in line with NFDS, we found that certain helminths that have recently colonized or spread in a given subpopulation, more frequently or intensely infected voles with MHC supertypes that have been common in the recent past. Overall, our results highlight complex spatial and temporal patterns of MHC-parasite associations, the latter being consistent with Red Queen coevolutionary dynamics.

Indexed as

ArvicolinaeHelminthsAnimalsHistocompatibility Antigens Class IIPolandPolymorphism, GeneticSelection, GeneticHistocompatibility Antigens Class IImajor histocompatibility complexMyodes glareolusnegative frequency-dependent selectionRed Queen

Identifiers

PMID35510766
PMCPMC9325469
OpenAlexW4229051572

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.