Evidence map›Paper›PMID 23147702›Full record

ReviewNature reviews. Microbiology2012

Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective.

Anders Folkesson, Lars Jelsbak, Lei Yang, Helle Krogh Johansen, Oana Ciofu, Niels Høiby, Søren Molin

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04803695 (Role of Pseudomonas Aeruginosa Biofilms in Exacerbations in Patients With Bronchiectasis With and Without Chronic Obstructive Pulmonary Disease), which is not on this map. Cited by 407 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
407citing papers in PubMed, 1 pooled it
–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.

NCT04803695 unknown statusnot on this mapstarted 2018, after this paper: background citation

Role of Pseudomonas Aeruginosa Biofilms in Exacerbations in Patients With Bronchiectasis With and Without Chronic Obstructive Pulmonary Disease

TypeobservationalSponsorHospital Clinic of BarcelonaRan2018 to 2021Enrolled96ConditionsBronchiectasis, Microbial Colonization, Pseudomonas Aeruginosa, BiofilmArmsMicrobial biofilm diagnose
3 · Its place in the literature

Who cites it

407 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. How cystic fibrosis modulator therapy could transformMicrobiology (Reading, England) · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Morphogenesis of bacterial colonies in liquid crystalline environments.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. R pyocin sensitivity ofJournal of medical microbiology · 2026
    Article
  10. Characterization of two exoUBMC microbiology · 2026
    Article
  11. Article
  12. ClpP2 modulates ClpXP assembly to promote multiple pathogenic phenotypes inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Essential role of cytochromeFrontiers in cellular and infection microbiology · 2026
    Article
  18. Article
  19. Article
  20. Within-host adaptation mutations associated with persistent colonization ofFrontiers in cellular and infection microbiology · 2026
    Article

347 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

7 authors.

Anders FolkessonDepartment of Systems Biology, Technical University of Denmark, 2800 Lyngby, Denmark.
Lars Jelsbak
Lei Yang
Helle Krogh Johansen
Oana Ciofu
Niels Høiby
Søren Molin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The airways of patients with cystic fibrosis (CF) are nearly always infected with many different microorganisms. This environment offers warm, humid and nutrient-rich conditions, but is also stressful owing to frequent antibiotic therapy and the host immune response. Pseudomonas aeruginosa is commonly isolated from the airways of patients with CF, where it most often establishes chronic infections that usually persist for the rest of the lives of the patients. This bacterium is a major cause of mortality and morbidity and has therefore been studied intensely. Here, we discuss how P. aeruginosa evolves from a state of early, recurrent intermittent colonization of the airways of patients with CF to a chronic infection state, and how this process offers opportunities to study bacterial evolution in natural environments. We believe that such studies are valuable not only for our understanding of bacterial evolution but also for the future development of new therapeutic strategies to treat severe chronic infections.

Indexed as

Biological EvolutionCystic FibrosisHost-Parasite InteractionsHumansPseudomonas aeruginosaPseudomonas InfectionsRespiratory System

Identifiers

PMID23147702

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.