Evidence map›Paper›PMID 24891445›Full record

ArticleJournal of bacteriology2014

The Pseudomonas aeruginosa diguanylate cyclase GcbA, a homolog of P. fluorescens GcbA, promotes initial attachment to surfaces, but not biofilm formation, via regulation of motility.

Olga E Petrova, Kathryn E Cherny, Karin Sauer

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

44 citing papers in PubMed, 68 citations in OpenAlex.

  1. Biofilm dispersion byJournal of bacteriology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. The surface interface and swimming motility influence surface-sensing responses inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Antibiotics (Basel, Switzerland) · 2024
    Review
  9. Article
  10. Adaption ofMicroorganisms · 2023
    Review
  11. A Library of Promoter-Applied and environmental microbiology · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Controlling Biofilm Development Through Cyclic di-GMP Signaling.Advances in experimental medicine and biology · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Olga E PetrovaDepartment of Biological Sciences, Binghamton University, Binghamton, New York, USA.
Kathryn E ChernyDepartment of Biological Sciences, Binghamton University, Binghamton, New York, USA.
Karin SauerDepartment of Biological Sciences, Binghamton University, Binghamton, New York, USA ksauer@binghamton.edu.
Binghamton University · US

Funding

Role of BdlA in biofilm dispersion and virulence properties of P. aeruginosaR01AI075257 · NIAID · STATE UNIVERSITY OF NY,BINGHAMTON · PI SAUER, KARIN · 2009 to 2012
$1.1M
NIAID NIH HHS 1R01 AI075257-01A2
6 · The paper itself

Abstract

Cyclic di-GMP is a conserved signaling molecule regulating the transitions between motile and sessile modes of growth in a variety of bacterial species. Recent evidence suggests that Pseudomonas species harbor separate intracellular pools of c-di-GMP to control different phenotypic outputs associated with motility, attachment, and biofilm formation, with multiple diguanylate cyclases (DGCs) playing distinct roles in these processes, yet little is known about the potential conservation of functional DGCs across Pseudomonas species. In the present study, we demonstrate that the P. aeruginosa homolog of the P. fluorescens DGC GcbA involved in promoting biofilm formation via regulation of swimming motility likewise synthesizes c-di-GMP to regulate surface attachment via modulation of motility, however, without affecting subsequent biofilm formation. P. aeruginosa GcbA was found to regulate flagellum-driven motility by suppressing flagellar reversal rates in a manner independent of viscosity, surface hardness, and polysaccharide production. P. fluorescens GcbA was found to be functional in P. aeruginosa and was capable of restoring phenotypes associated with inactivation of gcbA in P. aeruginosa to wild-type levels. Motility and attachment of a gcbA mutant strain could be restored to wild-type levels via overexpression of the small regulatory RNA RsmZ. Furthermore, epistasis analysis revealed that while both contribute to the regulation of initial surface attachment and flagellum-driven motility, GcbA and the phosphodiesterase DipA act within different signaling networks to regulate these processes. Our findings expand the complexity of c-di-GMP signaling in the regulation of the motile-sessile switch by providing yet another potential link to the Gac/Rsm network and suggesting that distinct c-di-GMP-modulating signaling pathways can regulate a single phenotypic output.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsBiofilmsCyclic GMPEscherichia coli ProteinsFlagellaGenetic Complementation TestMovementPhenotypePhosphoric Diester HydrolasesPhosphorus-Oxygen LyasesPolysaccharides, BacterialPolystyrenesPromoter Regions, GeneticPseudomonas aeruginosaSequence DeletionBacterial Proteinsbis(3',5')-cyclic diguanylic acidCyclic GMPdiguanylate cyclaseEscherichia coli ProteinsPhosphoric Diester HydrolasesPhosphorus-Oxygen LyasesPolysaccharides, BacterialPolystyrenes

Identifiers

PMID24891445
PMCPMC4135668
OpenAlexW2167248275

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.