Evidence map›Paper›PMID 25164818›Full record

ArticleThe Journal of biological chemistry2014

The pyruvate-tricarboxylic acid cycle node: a focal point of virulence control in the enteric pathogen Yersinia pseudotuberculosis.

René Bücker, Ann Kathrin Heroven, Judith Becker, Petra Dersch, Christoph Wittmann

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.1field-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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Function and Regulation of the Pyruvate Transporter CstA inInternational journal of molecular sciences · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. mBio · 2019
    Article
  16. Article
  17. Article
  18. Review
  19. BtsT, a Novel and Specific Pyruvate/HJournal of bacteriology · 2018
    Article
  20. Frontiers 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.

René BückerFrom the Institute of Systems Biotechnology, Saarland University, 66123 Saarbrücken, the Institute of Biochemical Engineering, Technische Universität, Braunschweig and.
Ann Kathrin Heroventhe Department of Molecular Infection Biology, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.
Judith BeckerFrom the Institute of Systems Biotechnology, Saarland University, 66123 Saarbrücken.
Petra Derschthe Department of Molecular Infection Biology, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany.
Christoph WittmannFrom the Institute of Systems Biotechnology, Saarland University, 66123 Saarbrücken, christoph.wittmann@uni-saarland.de.
Saarland University · DEHelmholtz Centre for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite our increasing knowledge of the specific pathogenicity factors in bacteria, the contribution of metabolic processes to virulence is largely unknown. Here, we elucidate a tight connection between pathogenicity and core metabolism in the enteric pathogen Yersinia pseudotuberculosis by integrated transcriptome and [(13)C]fluxome analysis of the wild type and virulence-regulator mutants. During aerobic growth on glucose, Y. pseudotuberculosis reveals an unusual flux distribution with a high level of secreted pyruvate. The absence of the transcriptional and post-transcriptional regulators RovA, CsrA, and Crp strongly perturbs the fluxes of carbon core metabolism at the level of pyruvate metabolism and the tricarboxylic acid (TCA) cycle, and these perturbations are accompanied by transcriptional changes in the corresponding enzymes. Knock-outs of regulators of this metabolic branch point and of its central enzyme, pyruvate kinase (ΔpykF), result in mutants with significantly reduced virulence in an oral mouse infection model. In summary, our work identifies the pyruvate-TCA cycle node as a focal point for controlling the host colonization and virulence of Yersinia.

Indexed as

Citric Acid CycleAdaptation, PhysiologicalAnimalsBacterial ProteinsBiomassEscherichia coliFemaleGene Expression Regulation, BacterialGene Regulatory NetworksGlucoseIronMetabolic Flux AnalysisMiceMice, Inbred BALB CMolecular WeightMutationBacterial ProteinsGlucoseIronPyruvatesBacteriaBacterial MetabolismBacterial PathogenesisGene ExpressionMetabolic Flux AnalysisPyruvateSystems BiologyTricarboxylic Acid Cycle (TCA Cycle) (Krebs Cycle)Yersinia

Identifiers

PMID25164818
PMCPMC4208018
OpenAlexW2002077151

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.