Evidence map›Paper›PMID 20732993›Full record

ArticleInfection and immunity2010

Specific resistance to Pseudomonas aeruginosa infection in zebrafish is mediated by the cystic fibrosis transmembrane conductance regulator.

Ryan T Phennicie, Matthew J Sullivan, John T Singer, Jeffrey A Yoder, Carol H Kim

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
  2. Cystic fibrosis: insights from zebrafish models.Disease models & mechanisms · 2026
    Review
  3. Strain-specific persistence ofJournal of medical microbiology · 2026
    Article
  4. Article
  5. Article
  6. Zebrafish (International journal of molecular sciences · 2024
    Review
  7. Localized Infections withInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Immunization againstIranian journal of basic medical sciences · 2021
    Article
  13. Zebrafish Embryo Infection Model to InvestigateFrontiers in cellular and infection microbiology · 2021
    Review
  14. Review
  15. Review
  16. Deletion ofFrontiers in immunology · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Dual Transcriptomics of Host-Pathogen Interaction of Cystic Fibrosis IsolateFrontiers in cellular and infection microbiology · 2018
    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

5 authors at 2 institutions in 1 country.

Ryan T PhennicieDepartment of Molecular and Biomedical Sciences, University of Maine, Orono, ME 04469, USA.
Matthew J Sullivan
John T Singer
Jeffrey A Yoder
Carol H Kim
University of Maine · USNorth Carolina State University · US

Funding

Quantitative Biology Research InstituteP20GM103534 · NIGMS · DARTMOUTH COLLEGE · PI AMOS, CHRISTOPHER I. · 2012 to 2016
$8.6M
Role of CFTR in Toxicant-Sensitivity of Innate ImmunityR21ES014028 · NIEHS · UNIVERSITY OF MAINE ORONO · PI KIM, CAROL H. · 2005 to 2006
$404k
NIEHS NIH HHS R21 ES014028NIEHS NIH HHS R21 ES014028-02NIGMS NIH HHS P20 GM103534
6 · The paper itself

Abstract

Cystic fibrosis (CF) is a genetic disease caused by recessive mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and is associated with prevalent and chronic Pseudomonas aeruginosa lung infections. Despite numerous studies that have sought to elucidate the role of CFTR in the innate immune response, the links between CFTR, innate immunity, and P. aeruginosa infection remain unclear. The present work highlights the zebrafish as a powerful model organism for human infectious disease, particularly infection by P. aeruginosa. Zebrafish embryos with reduced expression of the cftr gene (Cftr morphants) exhibited reduced respiratory burst response and directed neutrophil migration, supporting a connection between cftr and the innate immune response. Cftr morphants were infected with P. aeruginosa or other bacterial species that are commonly associated with infections in CF patients, including Burkholderia cenocepacia, Haemophilus influenzae, and Staphylococcus aureus. Intriguingly, the bacterial burden of P. aeruginosa was found to be significantly higher in zebrafish Cftr morphants than in controls, but this phenomenon was not observed with the other bacterial species. Bacterial burden in Cftr morphants infected with a P. aeruginosa ΔLasR mutant, a quorum sensing-deficient strain, was comparable to that in control fish, indicating that the regulation of virulence factors through LasR is required for enhancement of infection in the absence of Cftr. The zebrafish system provides a multitude of advantages for studying the pathogenesis of P. aeruginosa and for understanding the role that innate immune cells, such as neutrophils, play in the host response to acute bacterial infections commonly associated with cystic fibrosis.

Indexed as

Disease Models, AnimalAnimalsBacterial ProteinsCystic Fibrosis Transmembrane Conductance RegulatorHumansImmunity, InnateNeutrophilsPseudomonas aeruginosaPseudomonas InfectionsQuorum SensingTrans-ActivatorsVirulenceZebrafishBacterial ProteinsCystic Fibrosis Transmembrane Conductance RegulatorLasR protein, Pseudomonas aeruginosaTrans-Activators

Identifiers

PMID20732993
PMCPMC2976322
OpenAlexW2154315671

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.