Evidence map›Paper›PMID 21255280›Full record

ArticleMicrobial biotechnology2009

Three independent signalling pathways repress motility in Pseudomonas fluorescens F113.

Ana Navazo, Emma Barahona, Miguel Redondo-Nieto, Francisco Martínez-Granero, Rafael Rivilla, Marta Martín

Open access · bronzeAbstract read
In one paragraph

Article in Microbial biotechnology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

28 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Multiple Pathways Impact Swarming Motility ofbioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Adaption ofMicroorganisms · 2023
    Review
  7. Review
  8. Microorganisms · 2022
    Article
  9. Article
  10. International journal of molecular sciences · 2021
    Review
  11. Microbiology and molecular biology reviews : MMBR · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. SuhB Regulates the Motile-Sessile Switch inFrontiers in microbiology · 2017
    Article
  16. Frontiers in microbiology · 2016
    Article
  17. Article
  18. Article
  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

6 authors at 2 institutions in 2 countries.

Ana NavazoDepartamento de Biología. Universidad Autónoma de Madrid. c/Darwin, 2, 28049 Madrid, Spain.
Emma Barahona
Miguel Redondo-Nieto
Francisco Martínez-Granero
Rafael Rivilla
Marta Martín
Universidad Autónoma de Madrid · ESZero to Three · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motility is one of the most important traits for rhizosphere colonization by pseudomonads. Despite this importance, motility is severely repressed in the rhizosphere-colonizing strain Pseudomonas fluorescens F113. This bacterium is unable to swarm under laboratory conditions and produce relatively small swimming haloes. However, phenotypic variants with the ability to swarm and producing swimming haloes up to 300% larger than the wild-type strain, arise during rhizosphere colonization. These variants harbour mutations in the genes encoding the GacA/GacS two-component system and in other genes. In order to identify genes and pathways implicated in motility repression, we have used generalized mutagenesis with transposons. Analysis of the mutants has shown that besides the Gac system, the Wsp system and the sadB gene, which have been previously implicated in cyclic di-GMP turnover, are implicated in motility repression: mutants in the gacS, sadB or wspR genes can swarm and produce swimming haloes larger than the wild-type strain. Epistasis analysis has shown that the pathways defined by each of these genes are independent, because double and triple mutants show an additive phenotype. Furthermore, GacS, SadB and WspR act at different levels. Expression of the fleQ gene, encoding the master regulator of flagella synthesis is higher in the gacS(-) and sadB(-) backgrounds than in the wild-type strain and this differential expression is reflected by a higher secretion of the flagellin protein FliC. Conversely, no differences in fleQ expression or FliC secretion were observed between the wild-type strain and the wspR(-) mutant.

Indexed as

Gene Expression Regulation, BacterialLocomotionSignal TransductionBacterial Outer Membrane ProteinsBacterial ProteinsDNA Transposable ElementsMutagenesis, InsertionalMutant ProteinsMutationPseudomonas fluorescensTranscription FactorsBacterial Outer Membrane ProteinsBacterial ProteinsDNA Transposable ElementsGacA protein, BacterialemA protein, bacterialMutant ProteinsTranscription Factors

Identifiers

PMID21255280
PMCPMC3815909
OpenAlexW2028853237

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.