Evidence map›Paper›PMID 25705205›Full record

ArticleFrontiers in microbiology2015

FurA contributes to the oxidative stress response regulation of Mycobacterium avium ssp. paratuberculosis.

Elke Eckelt, Thorsten Meißner, Jochen Meens, Kristin Laarmann, Andreas Nerlich, Michael Jarek, Siegfried Weiss, Gerald-F Gerlach, Ralph Goethe

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. The role of transcriptional regulators in metal ion homeostasis ofFrontiers in cellular and infection microbiology · 2024
    Review
  4. Review
  5. Article
  6. Elucidating the Regulon of a FurFrontiers in microbiology · 2020
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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

9 authors at 3 institutions in 2 countries.

Elke EckeltInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Thorsten MeißnerInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Jochen MeensInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Kristin LaarmannInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Andreas NerlichInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Michael JarekGenome Analytics, Helmholtz Centre for Infection Research Braunschweig, Germany.
Siegfried WeissMolecular Immunology, Helmholtz Centre for Infection Research Braunschweig, Germany.
Gerald-F GerlachInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
Ralph GoetheInstitute for Microbiology, Department of Infectious Diseases, University of Veterinary Medicine Hannover Hannover, Germany.
University of Veterinary Medicine Hannover, Foundation · DEUniversity of Veterinary Medicine Vienna · ATHelmholtz Centre for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ferric uptake regulator A (FurA) is known to be involved in iron homeostasis and stress response in many bacteria. In mycobacteria the precise role of FurA is still unclear. In the presented study, we addressed the functional role of FurA in the ruminant pathogen Mycobacterium avium ssp. paratuberculosis (MAP) by construction of a furA deletion strain (MAPΔfurA). RNA deep sequencing revealed that the FurA regulon consists of repressed and activated genes associated to stress response or intracellular survival. Not a single gene related to metal homeostasis was affected by furA deletion. A decisive role of FurA during intracellular survival in macrophages was shown by significantly enhanced survival of MAPΔfurA compared to the wildtype, indicating that a principal task of mycobacterial FurA is oxidative stress response regulation in macrophages. This resistance was not associated with altered survival of mice after long term infection with MAP. Our results demonstrate for the first time, that mycobacterial FurA is not involved in the regulation of iron homeostasis. However, they provide strong evidence that FurA contributes to intracellular survival as an oxidative stress sensing regulator.

Indexed as

furAironmetallo-regulatormycobacteriaoxidative stress response regulation

Identifiers

PMID25705205
PMCPMC4319475
OpenAlexW2054189635

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.