Evidence map›Paper›PMID 32299345›Full record

ArticleBMC evolutionary biology2020

Host-parasite interactions in non-native invasive species are dependent on the levels of standing genetic variation at the immune locus.

Aleksandra Biedrzycka, Marcin Popiołek, Andrzej Zalewski

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Evidence of predation pressure on sensitive species by raccoons based on parasitological studies.International journal for parasitology. Parasites and wildlife · 2024
    Article
  8. Article
  9. Article
  10. Helminths in Invasive Raccoons (Pathogens (Basel, Switzerland) · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. 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

3 authors at 3 institutions in 1 country.

Aleksandra BiedrzyckaInstitute of Nature Conservation, Polish Academy of Sciences, Al. Adama Mickiewicza 33, 31-120, Kraków, Poland. biedrzycka@iop.krakow.pl.
Marcin PopiołekDepartment of Parasitology, Institute of Genetics and Microbiology, University of Wrocław, Przybyszewskiego 63/67, 51-148, Wroclaw, Poland.
Andrzej ZalewskiMammal Research Institute, Polish Academy of Sciences, ul. Stoczek 1, 17-230, Białowieża, Poland.
Mammal Research Institute · PLPolish Academy of Sciences · PLUniversity of Wrocław · PL

Funding

Narodowe Centrum Nauki 2014/15/B/NZ8/00261
6 · The paper itself

Abstract

backgroundParasites may mediate the success of biological invasions through their effect on host fitness and thus, on host population growth and stability. However, a release from the pressure of parasites is strongly related to the genetic differentiation of the host. In invasive host populations, the number of available genetic variants, allowing them to 'fight' the infection, are likely to be influenced by founder events and genetic drift. The level standing genetic variation of invasive populations may be crucial in successfully adapting to new environments and resisting diseases. We studied invasive populations of raccoon that experienced a random reduction in genetic diversity during the establishment and evaluated the relationship between host immune genetic diversity and intestinal parasites infection.

resultsWe distinguished two different genetic clusters that are characterized by different sets of functionally relevant MHC-DRB alleles. Both clusters were characterized by considerably different allele-parasite associations and different levels of parasite infection. The specific resistance MHC-DRB alleles explained the lower prevalence of Digenea parasites. An increased infection intensity was related to the presence of two MHC-DRB alleles. One of these alleles significantly decreased in frequency over time, causing a decrease of Digenea abundance in raccoons in consecutive years.

conclusionsOur findings suggest that intestinal parasites can exert selective pressure on an invasive host with lowered levels of immune genetic diversity and contribute to promoting local adaptation over time. The random genetic drift that created the two different genetic clusters in the invasive raccoon range imposed completely different MHC-parasite associations, strongly associated with the infection status of populations. Our findings underline the role of standing genetic variation in shaping host-parasite relationships and provide empirical support that functional genetic variation may be, at least partly, responsible for differences in the success of invasive populations.

Indexed as

Genetic VariationHost-Parasite InteractionsIntroduced SpeciesAllelesAnimalsIntestinesMultigene FamilyParasitesRaccoonsSelection, GeneticCestodaDigeneaGenetic driftImmune genetic diversityIntestinal parasitesInvasive populationsMHC-DRBRaccoonStanding genetic variation

Identifiers

PMID32299345
PMCPMC7164242
OpenAlexW3016808616

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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.