Evidence map›Paper›PMID 26042786›Full record

ArticlePLoS biology2015

Host-Pathogen Coevolution: The Selective Advantage of Bacillus thuringiensis Virulence and Its Cry Toxin Genes.

Leila Masri, Antoine Branca, Anna E Sheppard, Andrei Papkou, David Laehnemann, Patrick S Guenther, Swantje Prahl, Manja Saebelfeld, Jacqueline Hollensteiner, Heiko Liesegang and 9 more

Abstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Article
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  9. Article
  10. Evolutionary repeatability of emergent properties of ecological communities.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. What Can Genetics Do for the Control of Infectious Diseases in Aquaculture?Animals : an open access journal from MDPI · 2022
    Review
  15. No major cost of evolved survivorship inProceedings. Biological sciences · 2022
    Article
  16. Article
  17. Article
  18. Exploring Effects ofFrontiers in cellular and infection microbiology · 2022
    Article
  19. Population size impacts host-pathogen coevolution.Proceedings. Biological sciences · 2021
    Article
  20. 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

19 authors.

Leila MasriDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany; Department of Animal Evolutionary Ecology, Institute of Evolution and Ecology, University of Tuebingen, Tuebingen, Germany.
Antoine BrancaInstitute for Evolution and Biodiversity, University of Muenster, Muenster, Germany.
Anna E SheppardDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Andrei PapkouDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
David LaehnemannDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany; Department of Animal Evolutionary Ecology, Institute of Evolution and Ecology, University of Tuebingen, Tuebingen, Germany.
Patrick S GuentherDepartment of Animal Evolutionary Ecology, Institute of Evolution and Ecology, University of Tuebingen, Tuebingen, Germany.
Swantje PrahlDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Manja SaebelfeldDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Jacqueline HollensteinerGoettingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University of Goettingen, Goettingen, Germany.
Heiko LiesegangGoettingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University of Goettingen, Goettingen, Germany.
Elzbieta BrzuszkiewiczGoettingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University of Goettingen, Goettingen, Germany.
Rolf DanielGoettingen Genomics Laboratory, Institute of Microbiology and Genetics, Georg-August-University of Goettingen, Goettingen, Germany.
Nicolaas K MichielsDepartment of Animal Evolutionary Ecology, Institute of Evolution and Ecology, University of Tuebingen, Tuebingen, Germany.
Rebecca D SchulteDepartment of Behavioural Biology, University of Osnabrueck, Osnabrueck, Germany.
Joachim KurtzInstitute for Evolution and Biodiversity, University of Muenster, Muenster, Germany.
Philip RosenstielInstitute for Clinical Molecular Biology, Christian-Albrechts-University, Kiel, Germany.
Arndt TelschowInstitute for Evolution and Biodiversity, University of Muenster, Muenster, Germany.
Erich Bornberg-BauerInstitute for Evolution and Biodiversity, University of Muenster, Muenster, Germany.
Hinrich SchulenburgDepartment of Evolutionary Ecology and Genetics, Zoological Institute, Christian-Albrechts-University of Kiel, Kiel, Germany; Department of Animal Evolutionary Ecology, Institute of Evolution and Ecology, University of Tuebingen, Tuebingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reciprocal coevolution between host and pathogen is widely seen as a major driver of evolution and biological innovation. Yet, to date, the underlying genetic mechanisms and associated trait functions that are unique to rapid coevolutionary change are generally unknown. We here combined experimental evolution of the bacterial biocontrol agent Bacillus thuringiensis and its nematode host Caenorhabditis elegans with large-scale phenotyping, whole genome analysis, and functional genetics to demonstrate the selective benefit of pathogen virulence and the underlying toxin genes during the adaptation process. We show that: (i) high virulence was specifically favoured during pathogen-host coevolution rather than pathogen one-sided adaptation to a nonchanging host or to an environment without host; (ii) the pathogen genotype BT-679 with known nematocidal toxin genes and high virulence specifically swept to fixation in all of the independent replicate populations under coevolution but only some under one-sided adaptation; (iii) high virulence in the BT-679-dominated populations correlated with elevated copy numbers of the plasmid containing the nematocidal toxin genes; (iv) loss of virulence in a toxin-plasmid lacking BT-679 isolate was reconstituted by genetic reintroduction or external addition of the toxins. We conclude that sustained coevolution is distinct from unidirectional selection in shaping the pathogen's genome and life history characteristics. To our knowledge, this study is the first to characterize the pathogen genes involved in coevolutionary adaptation in an animal host-pathogen interaction system.

Indexed as

Biological EvolutionSelection, GeneticAnimalsBacillus thuringiensisBacterial ProteinsCaenorhabditis elegansGenome, BacterialGenomicsGenotypeHost-Pathogen InteractionsInsect ProteinsPhenotypeReceptors, Cell SurfaceVirulenceBacterial ProteinsCry toxin receptorsInsect ProteinsReceptors, Cell Surface

Identifiers

PMID26042786
PMCPMC4456383

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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.