Evidence map›Paper›PMID 25039394›Full record

ArticleMolecular microbiology2014

EspI regulates the ESX-1 secretion system in response to ATP levels in Mycobacterium tuberculosis.

Ming Zhang, Jeffrey M Chen, Claudia Sala, Jan Rybniker, Neeraj Dhar, Stewart T Cole

Open access · greenAbstract read
In one paragraph

Article in Molecular microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  5. Phase variation as a major mechanism of adaptation inProceedings of the National Academy of Sciences of the United States of America · 2023
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  9. Comparative Genome Analyses ofFrontiers in microbiology · 2021
    Article
  10. Article
  11. Modeling Tubercular ESX-1 Secretion Using Mycobacterium marinum.Microbiology and molecular biology reviews : MMBR · 2020
    Review
  12. Review
  13. Genomic Insights Into theFrontiers in microbiology · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Identification of genes required forProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. The Role of ESX-1 inMicrobiology spectrum · 2017
    Review
  19. Article
  20. Review
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 1 institution in 2 countries.

Ming Zhang *Ecole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
Jeffrey M Chen *Ecole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
Claudia SalaEcole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
Jan RybnikerEcole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
Neeraj DharEcole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
Stewart T ColeEcole Polytechnique Fédérale de Lausanne, Global Health Institute, Station 19, CH-1015, Lausanne, Switzerland.
École Polytechnique Fédérale de Lausanne · CH

Funding

CIHRNIAID NIH HHS HHSN266200400091C
6 · The paper itself

Abstract

The function of EspI, a 70 kDa protein in Mycobacterium tuberculosis, has remained unclear. Although EspI is encoded by a gene within the esx-1 locus, in this study we clarify previous conflicting results and show that EspI is not essential for ESX-1-mediated secretion or virulence in M. tuberculosis. We also provide evidence that reduction of cellular ATP levels in wild-type M. tuberculosis using the drug bedaquiline completely blocks ESX-1-mediated secretion. Remarkably, M. tuberculosis lacking EspI fails to exhibit this phenotype. Furthermore, mutagenesis of a highly conserved ATP-binding motif in EspI renders M. tuberculosis incapable of shutting down ESX-1-mediated secretion during ATP depletion. Collectively these results show that M. tuberculosis EspI negatively regulates the ESX-1 secretion system in response to low cellular ATP levels and this function requires the ATP-binding motif. In light of our results the potential significance of EspI in ESX-1 function during latent tuberculosis infection and reactivation is also discussed.

Indexed as

Bacterial Secretion SystemsGene Expression Regulation, BacterialAdenosine TriphosphateAmino Acid SequenceBacterial ProteinsMolecular Sequence DataMycobacterium tuberculosisSequence AlignmentSignal TransductionAdenosine TriphosphateBacterial ProteinsBacterial Secretion Systems

Identifiers

PMID25039394
PMCPMC4150839
OpenAlexW1928554269

What OpenQuestion holds

Textmetadata
LicenceTDM
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.