Evidence map›Paper›PMID 15995954›Full record

ArticleThe Journal of infectious diseases2005

Nonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model.

Alessandra Bragonzi, Dieter Worlitzsch, Gerald B Pier, Petra Timpert, Martina Ulrich, Morten Hentzer, Jens Bo Andersen, Michael Givskov, Massimo Conese, Gerd Doring

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 140 citations in OpenAlex.

  1. Article
  2. The longitudinal expression ofMicrobiology (Reading, England) · 2026
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  4. Assessing the Potential ofACS pharmacology & translational science · 2024
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  7. Microbiology spectrum · 2023
    Article
  8. To bead or not to bead: A review ofFrontiers in physiology · 2023
    Review
  9. The cystic fibrosis lung microenvironment alters antibiotic activity: causes and effects.European respiratory review : an official journal of the European Respiratory Society · 2021
    Review
  10. Article
  11. The Response ofInternational journal of molecular sciences · 2020
    Article
  12. Article
  13. A New Model of ChronicInternational journal of molecular sciences · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Frontiers in microbiology · 2020
    Article
  20. Article

13 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

10 authors at 5 institutions in 4 countries.

Alessandra BragonziInstitute of Medical Microbiology and Hygiene, Universitatsklinikum Tubingen, Germany.
Dieter Worlitzsch
Gerald B Pier
Petra Timpert
Martina Ulrich
Morten Hentzer
Jens Bo Andersen
Michael Givskov
Massimo Conese
Gerd Doring
Universitätsklinikum Tübingen · DETechnical University of Denmark · DKHarvard University · USInstitute of Medical Microbiology and Hygiene · DEVita-Salute San Raffaele University · IT

Funding

VIRULENCE AND IMMUNITY TO MUCOID P. AERUGINOSAR01AI048917 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 2001 to 2009
$3.2M
NIAID NIH HHS AI48917NIAID NIH HHS R01 AI048917
6 · The paper itself

Abstract

backgroundIn patients with cystic fibrosis (CF), lung infection with mucoid Pseudomonas aeruginosa strains overexpressing the exopolysaccaride alginate is preceded by colonization with nonmucoid strains. We investigated the kinetics, impact of environmental signals, and genetics of P. aeruginosa alginate expression in a mouse model and in patients with CF.

methodsUsing indirect immunofluorescence, microarray technology and real-time reverse-transcription polymerase chain reaction, we assessed alginate gene expression during aerobic and anaerobic growth of the nonmucoid strain PAO1 in vitro, in a mouse lung-infection model and in sputum specimens from patients with CF infected with nonmucoid or mucoid P. aeruginosa strains.

resultsAnaerobic conditions increased the transcription of alginate genes in vitro and in murine lungs within 24 h. Alginate production by PAO1 in murine lungs and by nonmucoid P. aeruginosa strains in patients with CF was reversible after in vitro culture under aerobic conditions. A subpopulation of P. aeruginosa clones revealing stable alginate production was detected in murine lungs 2 weeks after infection.

conclusionsAnaerobiosis and lung infection rapidly induce alginate production by gene regulation in nonmucoid P. aeruginosa. This trait may contribute to early persistence, leading to chronic P. aeruginosa infection once stable mucoid strains are generated.

Indexed as

AlginatesAnimalsBacteroides fragilisCystic FibrosisDisease Models, AnimalGene Expression RegulationHumansLungMicePseudomonas aeruginosaSputumAlginates

Identifiers

PMID15995954
PMCPMC1317300
OpenAlexW2156039720

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.