Evidence map›Paper›PMID 29237286›Full record

ArticleAntioxidants & redox signaling2018

Redox-Sensing Under Hypochlorite Stress and Infection Conditions by the Rrf2-Family Repressor HypR in Staphylococcus aureus.

Vu Van Loi, Tobias Busche, Karsten Tedin, Jörg Bernhardt, Jan Wollenhaupt, Nguyen Thi Thu Huyen, Christoph Weise, Jörn Kalinowski, Markus C Wahl, Marcus Fulde and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Antioxidants & redox signaling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 60 citations in OpenAlex.

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  11. The Catalase KatA Contributes to Microaerophilic HAntioxidants (Basel, Switzerland) · 2022
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  16. The Old Yellow Enzyme OfrA FostersFrontiers in microbiology · 2022
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  19. Review
  20. SigB-regulated antioxidant functions in gram-positive bacteria.World journal of microbiology & biotechnology · 2021
    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

11 authors at 3 institutions in 1 country.

Vu Van Loi1 Institute for Biology-Microbiology, Freie Universität Berlin , Berlin, Germany .
Tobias Busche1 Institute for Biology-Microbiology, Freie Universität Berlin , Berlin, Germany .
Karsten Tedin3 Centre for Infection Medicine, Institute of Microbiology and Epizootics , Freie Universität Berlin, Berlin, Germany .
Jörg Bernhardt4 Institute for Microbiology, Ernst-Moritz-Arndt-University of Greifswald , Greifswald, Germany .
Jan Wollenhaupt5 Laboratory of Structural Biochemistry, Freie Universität Berlin, Berlin, Germany .
Nguyen Thi Thu Huyen1 Institute for Biology-Microbiology, Freie Universität Berlin , Berlin, Germany .
Christoph Weise6 Institute of Chemistry and Biochemistry , Freie Universität Berlin, Berlin, Germany .
Jörn Kalinowski2 Center for Biotechnology, Bielefeld University , Bielefeld, Germany .
Markus C Wahl5 Laboratory of Structural Biochemistry, Freie Universität Berlin, Berlin, Germany .
Marcus Fulde3 Centre for Infection Medicine, Institute of Microbiology and Epizootics , Freie Universität Berlin, Berlin, Germany .
Haike Antelmann1 Institute for Biology-Microbiology, Freie Universität Berlin , Berlin, Germany .
Freie Universität Berlin · DEBielefeld University · DEUniversität Greifswald · DE

Funding

European Research Council 615585
6 · The paper itself

Abstract

aimsStaphylococcus aureus is a major human pathogen and has to cope with reactive oxygen and chlorine species (ROS, RCS) during infections, which requires efficient protection mechanisms to avoid destruction. Here, we have investigated the changes in the RNA-seq transcriptome by the strong oxidant sodium hypochlorite (NaOCl) in S. aureus USA300 to identify novel redox-sensing mechanisms that provide protection under infection conditions.

resultsNaOCl stress caused an oxidative stress response in S. aureus as indicated by the induction of the PerR, QsrR, HrcA, and SigmaB regulons in the RNA-seq transcriptome. The hypR-merA (USA300HOU_0588-87) operon was most strongly upregulated under NaOCl stress, which encodes for the Rrf2-family regulator HypR and the pyridine nucleotide disulfide reductase MerA. We have characterized HypR as a novel redox-sensitive repressor that controls MerA expression and directly senses and responds to NaOCl and diamide stress via a thiol-based mechanism in S. aureus. Mutational analysis identified Cys33 and the conserved Cys99 as essential for NaOCl sensing, while Cys99 is also important for repressor activity of HypR in vivo. The redox-sensing mechanism of HypR involves Cys33-Cys99 intersubunit disulfide formation by NaOCl stress both in vitro and in vivo. Moreover, the HypR-controlled flavin disulfide reductase MerA was shown to protect S. aureus against NaOCl stress and increased survival in J774A.1 macrophage infection assays. Conclusion and Innovation: Here, we identified a new member of the widespread Rrf2 family as redox sensor of NaOCl stress in S. aureus that uses a thiol/disulfide switch to regulate defense mechanisms against the oxidative burst under infections in S. aureus. Antioxid. Redox Signal. 29, 615-636.

Indexed as

AnimalsBacterial ProteinsCell LineComputational BiologyHypochlorous AcidMiceModels, MolecularOxidation-ReductionOxidative StressStaphylococcal InfectionsStaphylococcus aureusBacterial ProteinsHypochlorous Acidhypochlorite stressredox-sensing regulatorRrf2Staphylococcus aureus

Identifiers

PMID29237286
PMCPMC6067689
OpenAlexW2775676425

What OpenQuestion holds

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LicenceCC BY-NC
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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.