Evidence map›Paper›PMID 12093875›Full record

ArticleThe Journal of experimental medicine2002

Multidrug efflux systems play an important role in the invasiveness of Pseudomonas aeruginosa.

Yoichi Hirakata, Ramakrishnan Srikumar, Keith Poole, Naomasa Gotoh, Takashi Suematsu, Shigeru Kohno, Shimeru Kamihira, Robert E W Hancock, David P Speert

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
6.7field-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

128 citing papers in PubMed, 256 citations in OpenAlex.

  1. Strain-specific persistence ofJournal of medical microbiology · 2026
    Article
  2. Antibiotic Resistance inAntibiotics (Basel, Switzerland) · 2026
    Review
  3. Review
  4. Genomic characterization ofAdvances in laboratory medicine · 2025
    Article
  5. Advances in laboratory medicine · 2025
    Article
  6. Article
  7. Biliary microbiota in disease-free, obstructive and post-drainage biliary tracts.Frontiers in cellular and infection microbiology · 2025
    Article
  8. Antibiotics (Basel, Switzerland) · 2024
    Review
  9. Article
  10. Review
  11. Evidence for intracellularJournal of bacteriology · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. RND pumps across the genusMicrobial genomics · 2023
    Article
  18. Review
  19. Review
  20. Article

68 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 at 4 institutions in 2 countries.

Yoichi HirakataDivision of Infectious and Immunological Diseases, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, V5Z 4H4 Canada. hirakata@net.nagasaki-u.ac.jp
Ramakrishnan Srikumar
Keith Poole
Naomasa Gotoh
Takashi Suematsu
Shigeru Kohno
Shimeru Kamihira
Robert E W Hancock
David P Speert
Nagasaki University · JPUniversity of British Columbia · CAQueen's University · CAKyoto Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudomonas aeruginosa is an important opportunistic human pathogen. Certain strains can transmigrate across epithelial cells, and their invasive phenotype is correlated with capacity to cause invasive human disease and fatal septicemia in mice. Four multidrug efflux systems have been described in P. aeruginosa, however, their contribution to virulence is unclear. To clarify the role of efflux systems in invasiveness, P. aeruginosa PAO1 wild-type (WT) and its efflux mutants were evaluated in a Madin-Darby canine kidney (MDCK) epithelial cell monolayer system and in a murine model of endogenous septicemia. All efflux mutants except a deltamexCD-oprJ deletion demonstrated significantly reduced invasiveness compared with WT. In particular, a deltamexAB-oprM deletion strain was compromised in its capacity to invade or transmigrate across MDCK cells, and could not kill mice, in contrast to WT which was highly invasive (P < 0.0006) and caused fatal infection (P < 0.0001). The other mutants, including deltamexB and deltamexXY mutants, were intermediate between WT and the deltamexAB-oprM mutant in invasiveness and murine virulence. Invasiveness was restored to the deltamexAB-oprM mutant by complementation with mexAB-oprM or by addition of culture supernatant from MDCK cells infected with WT. We conclude that the P. aeruginosa MexAB-OprM efflux system exports virulence determinants that contribute to bacterial virulence.

Indexed as

Membrane Transport ProteinsAnimalsBacterial Outer Membrane ProteinsBacterial ProteinsBacterial TranslocationCarrier ProteinsCell LineCulture Media, ConditionedDisease Models, AnimalDisease ProgressionDogsDrug Resistance, BacterialEpithelial CellsGentamicinsKidneyMiceBacterial Outer Membrane ProteinsBacterial ProteinsCarrier ProteinsCulture Media, ConditionedGentamicinsMembrane Transport ProteinsMexA protein, Pseudomonas aeruginosaMexB protein, Pseudomonas aeruginosa

Identifiers

PMID12093875
PMCPMC2194012
OpenAlexW2112882791

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.