Evidence map›Paper›PMID 28548661›Full record

ArticleThe ISME journal2017

Co-evolution with Staphylococcus aureus leads to lipopolysaccharide alterations in Pseudomonas aeruginosa.

Mikael Tognon, Thilo Köhler, Bartosz G Gdaniec, Youai Hao, Joseph S Lam, Marie Beaume, Alexandre Luscher, Angus Buckling, Christian van Delden

Abstract read
In one paragraph

Article in The ISME journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Microenvironment shapesiScience · 2026
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  2. Calprotectin protectsmSystems · 2025
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  8. The evolution of autonomy from two cooperative specialists in fluctuating environments.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. The presence of cystic fibrosis-related diabetes modifies the sputum microbiome in cystic fibrosis disease.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  10. A bacterial pigment provides cross-species protection from HProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Co-occurring microflora and mucin driveISME communications · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. AIMS microbiology · 2023
    Review
  19. Review
  20. Article

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

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

9 authors.

Mikael TognonTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.
Thilo KöhlerTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.
Bartosz G GdaniecTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.
Youai HaoDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.
Joseph S LamDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.
Marie BeaumeTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.
Alexandre LuscherTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.
Angus BucklingEnvironment and Sustainability Institute, University of Exeter, Penryn, UK.
Christian van DeldenTransplant Infectious Diseases Unit, University Hospitals of Geneva, Genève, Switzerland.

Funding

CIHR MOP-14687
6 · The paper itself

Abstract

Detrimental and beneficial interactions between co-colonizing bacteria may influence the course of infections. In cystic fibrosis (CF) airways, Staphylococcus aureus prevails in childhood, whereas Pseudomonas aeruginosa progressively predominates thereafter. While a range of interactions has been identified, it is unclear if these represent specific adaptations or correlated responses to other aspects of the environment. Here, we investigate how P. aeruginosa adapts to S. aureus by evolving P. aeruginosa in the presence and absence of S. aureus. P. aeruginosa populations that evolved for 150 generations were sequenced and compared to the ancestor strain. Mutations in the Wsp signaling system were identified in both treatments and likely occurred because of low oxygen availability. Despite showing increased killing activity, wsp mutants were less fit in the presence of S. aureus. In contrast, mutations in lipopolysaccharide (LPS) biosynthesis occurred exclusively in co-cultures with S. aureus and conferred a fitness gain in its presence. Moreover, they increased resistance towards beta-lactam antibiotics. Strikingly, both mutations in wsp and LPS genes are observed in clinical isolates from CF-patients. Our results suggest that P. aeruginosa LPS mutations are a direct consequence of S. aureus imposed selection in vitro.

Indexed as

LipopolysaccharidesPseudomonas aeruginosaStaphylococcus aureusBiological CoevolutionCoculture TechniquesCystic FibrosisMutationPseudomonas InfectionsStaphylococcal InfectionsLipopolysaccharides

Identifiers

PMID28548661
PMCPMC5607365

What OpenQuestion holds

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Registered trials

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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.