Evidence map›Paper›PMID 42755362›Full record

ArticleNucleic acids research2026

A Zur-dependent regulatory RNA involved in maintaining zinc homeostasis in Staphylococcus aureus.

Mathilde Charbonnier, Hugo Racine, Samuel Probst-Lotze, Jana N Radin, Gustavo Rios-Delgado, Liangyu Lyu, Hannah M Laster, Maximilian P Kohl, Rafał Mazgaj, Marion Blum and 11 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Mathilde CharbonnierUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.ORCID 0000-0002-2211-1196
Hugo RacineUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Samuel Probst-LotzeUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Jana N RadinDepartment of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United States.
Gustavo Rios-DelgadoDepartment of Biochemistry and Microbiology, Rutgers, the State University of New Jersey, New Brunswick, NJ 08901, United States.
Liangyu LyuDepartment of Biochemistry and Microbiology, Rutgers, the State University of New Jersey, New Brunswick, NJ 08901, United States.
Hannah M LasterDepartment of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United States.
Maximilian P KohlUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Rafał MazgajLaboratory of Metalloprotein Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw 02-106, Poland.
Marion BlumUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Virginie MarchandIMoPA UMR7365 CNRS-UL, BioPole Université de Lorraine, Vandœuvre-lès-Nancy 54505, France.
Johana ChicherPlateforme de Protéomique Strasbourg-Esplanade, CNRS UAR1589, F-67000 Strasbourg, France.ORCID 0000-0002-4403-7484
Pascale RombyUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Stefano MarziUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.
Isabelle CaldelariUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.ORCID 0000-0002-1427-4569
Jai J TreeSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.ORCID 0000-0001-8233-0975
Kevin J WaldronLaboratory of Metalloprotein Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw 02-106, Poland.ORCID 0000-0002-5577-7357
Jeffrey M BoydDepartment of Biochemistry and Microbiology, Rutgers, the State University of New Jersey, New Brunswick, NJ 08901, United States.ORCID 0000-0001-7721-3926
Julien Y DutheilDepartment of Theoretical Biology, Max Planck Institute of Evolutionary Biology, Plön D-24306, Germany.ORCID 0000-0001-7753-4121
Thomas E Kehl-FieDepartment of Microbiology and Immunology, Carver College of Medicine, University of Iowa, Iowa City, IA 52242, United States.
David LalaounaUniversité de Strasbourg, CNRS, Architecture et Réactivité de l'ARN, UPR9002, F-67000 Strasbourg, France.ORCID 0000-0002-0347-5816

Funding

Calprotectin and Antibiotic Activities at the Infection InterfaceR01AI179695 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Brian Patrick Conlon, Thomas Everett Kehl-Fie · 2024 to 2026
$2.3M
Agence Nationale de la Recherche ANR-20-CE12-0021Australian Research Council DP220101938EUR IMCBio ANR-17-EURE-0023Interdisciplinary Thematic Institute IMCBio+ ANR-10-IDEX-0002National Health and Medical Research Council GNT2028572NIAID NIH HHS R01 AI179695NIAID NIH HHS R01AI179695SFRI-STRAT'US ANR-20-SFRI-0012Thomas Jefferson Fund ANR-10-IDEX-0002University of Iowa's Year 2 P3 Strategic Initiatives Program GNT2028572University of Strasbourg, CNRS and Inserm, IdEx Unistra ANR-10-IDEX-0002
6 · The paper itself

Abstract

Small regulatory RNAs (sRNAs) are key drivers of bacterial adaptation to environmental fluctuations, including iron and manganese restriction imposed by the host. This study explored the repertoire of sRNAs produced by the human pathogen Staphylococcus aureus in response to metal limitation. Two sRNAs were identified, S1077 and ZinS, that were regulated by zinc (Zn) availability. Further investigations revealed that, similar to the cnt operon from which it derives, S1077 synthesis is controlled by the transcription factors Zur and Fur. In contrast, zinS transcription is solely repressed by Zur. RNA affinity purification identified several ZinS-associated mRNAs encoding Zn-dependent enzymes, including the alcohol dehydrogenase Adh, whose synthesis is negatively regulated by ZinS. Loss of ZinS does not alter staphylococcal metal accumulation, suggesting a role in a Zn-sparing response. Remarkably, zinS also encodes a small peptide, ZinP. Genomic analysis shows that the regulatory portion of zinS emerged from the 3' untranslated region of zinP and is conserved in S. aureus and closely related species, whereas zinP is also found in phylogenetically distant organisms. Our findings demonstrate that sRNAs facilitate bacterial adaptation to Zn limitation, and that genetic exchange and subsequent neofunctionalization have enabled S. aureus to adapt to metal-restricted environments.

Indexed as

Bacterial ProteinsRNA, BacterialRNA, Small UntranslatedStaphylococcus aureusZinc3' Untranslated RegionsAlcohol DehydrogenaseBase SequenceGene Expression Regulation, BacterialHomeostasisRepressor Proteins3' Untranslated RegionsAlcohol DehydrogenaseBacterial ProteinsRepressor ProteinsRNA, BacterialRNA, Small UntranslatedZinc

Identifiers

PMID42755362
PMCPMC13586535

What OpenQuestion holds

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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.