Evidence map›Paper›PMID 24920832›Full record

ArticleNucleic acids research2014

GtrS and GltR form a two-component system: the central role of 2-ketogluconate in the expression of exotoxin A and glucose catabolic enzymes in Pseudomonas aeruginosa.

Abdelali Daddaoua, Carlos Molina-Santiago, Jesús de la Torre, Tino Krell, Juan-Luis Ramos

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. mBio · 2024
    Article
  8. Transcriptional Regulators Controlling Virulence inInternational journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Commensal colonization reducesFrontiers in cellular and infection microbiology · 2023
    Article
  14. Article
  15. Review
  16. Review
  17. Virulence Factors ofFrontiers in cellular and infection microbiology · 2022
    Review
  18. Role of Two-Component System Networks in Pseudomonas aeruginosa Pathogenesis.Advances in experimental medicine and biology · 2022
    Article
  19. Roles of Two-Component Systems inInternational journal of molecular sciences · 2021
    Review
  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

5 authors at 1 institution in 1 country.

Abdelali DaddaouaDepartment of Environmental Protection, CSIC-EEZ, C/Profesor Albareda 1, E-18008 Granada, Spain abdelali.daddaoua@eez.csic.es.
Carlos Molina-SantiagoDepartment of Environmental Protection, CSIC-EEZ, C/Profesor Albareda 1, E-18008 Granada, Spain.
Jesús de la TorreDepartment of Environmental Protection, CSIC-EEZ, C/Profesor Albareda 1, E-18008 Granada, Spain.
Tino KrellDepartment of Environmental Protection, CSIC-EEZ, C/Profesor Albareda 1, E-18008 Granada, Spain.
Juan-Luis RamosDepartment of Environmental Protection, CSIC-EEZ, C/Profesor Albareda 1, E-18008 Granada, Spain.
Consejo Superior de Investigaciones Científicas · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the human pathogen Pseudomonas aeruginosa, the GltR regulator is required for glucose transport, whereas GtrS is a sensor kinase that plays a key role in mediating bacteria-host interaction and pathogen dissemination in the host. We show that GtrS and GltR form a two-component system that regulates the expression from the promoters Pedd/gap-1, PoprB and Pglk, which control the expression of genes involved in glucose metabolism and transport. In addition, the GtrS/GltR pair regulates the expression of toxA that encodes exotoxin A, the primary virulence factor. Microcalorimetry-based ligand screening of the recombinant GtrS ligand-binding domain revealed specific binding of 2-ketogluconate (2-KG) (KD=5 μM) and 6-phosphogluconate (KD=98 μM). These effectors accelerate GtrS autophosphorylation, with concomitant transphosphorylation of GltR leading to a three-fold increase in transcription. Surprisingly, in vivo a similar increase in expression from the above promoters was observed for the mutant deficient in GltR regardless of the presence of effectors. The GltR operator site was found to contain the consensus sequence 5'-tgGTTTTTc-3'. We propose that 2-KG is a key metabolite in the stringent transcriptional control of genes involved in virulence and glucose metabolism. We show that GltR is a transcriptional repressor that is released from DNA upon phosphorylation.

Indexed as

Gene Expression Regulation, BacterialADP Ribose TransferasesBacterial ProteinsBacterial ToxinsBinding SitesExotoxinsGluconatesGlucoseMonosaccharide Transport ProteinsPromoter Regions, GeneticProtein KinasesProtein Structure, TertiaryPseudomonas aeruginosaPseudomonas aeruginosa Exotoxin ARepressor ProteinsTranscriptional Activation2-ketogluconate6-phosphogluconic acidADP Ribose TransferasesBacterial ProteinsBacterial ToxinsExotoxinsGltR protein, Pseudomonas aeruginosaGluconatesGlucoseMonosaccharide Transport ProteinsProtein KinasesPseudomonas aeruginosa Exotoxin ARepressor ProteinsVirulence Factors

Identifiers

PMID24920832
PMCPMC4081096
OpenAlexW2153078195

What OpenQuestion holds

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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.