Evidence map›Paper›PMID 30443649›Full record

ArticleMetallomics : integrated biometal science2019

Copper stress in Staphylococcus aureus leads to adaptive changes in central carbon metabolism.

Emma Tarrant, Gustavo P Riboldi, Matthew R McIlvin, Jack Stevenson, Anna Barwinska-Sendra, Louisa J Stewart, Mak A Saito, Kevin J Waldron

Open access · hybridAbstract read
In one paragraph

Article in Metallomics : integrated biometal science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  3. Review
  4. mSphere · 2026
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  8. Microbial metal physiology: ions to ecosystems.Nature reviews. Microbiology · 2025
    Review
  9. Article
  10. Article
  11. Article
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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

8 authors at 2 institutions in 2 countries.

Emma TarrantInstitute for Cell & Molecular Biosciences, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK. kevin.waldron@ncl.ac.uk.
Gustavo P Riboldi
Matthew R McIlvin
Jack Stevenson
Anna Barwinska-Sendra
Louisa J Stewart
Mak A Saito
Kevin J Waldron
In-Q-Tel · USWoodwell Climate Research Center · US

Funding

Biotechnology and Biological Sciences Research Council BB/F015895/1Biotechnology and Biological Sciences Research Council BB/J014516/1Wellcome Trust 098375/Z/12/Z
6 · The paper itself

Abstract

Copper toxicity has been a long-term selection pressure on bacteria due to its presence in the environment and its use as an antimicrobial agent by grazing protozoa, by phagocytic cells of the immune system, and in man-made medical and commercial products. There is recent evidence that exposure to increased copper stress may have been a key driver in the evolution and spread of methicillin-resistant Staphylococcus aureus, a globally important pathogen that causes significant mortality and morbidity worldwide. Yet it is unclear how S. aureus physiology is affected by copper stress or how it adapts in order to be able to grow in the presence of excess copper. Here, we have determined quantitatively how S. aureus alters its proteome during growth under copper stress conditions, comparing this adaptive response in two different types of growth regime. We found that the adaptive response involves induction of the conserved copper detoxification system as well as induction of enzymes of central carbon metabolism, with only limited induction of proteins involved in the oxidative stress response. Further, we identified a protein that binds copper inside S. aureus cells when stressed by copper excess. This copper-binding enzyme, a glyceraldehyde-3-phosphate dehydrogenase essential for glycolysis, is inhibited by copper in vitro and inside S. aureus cells. Together, our data demonstrate that copper stress leads to the inhibition of glycolysis in S. aureus, and that the bacterium adapts to this stress by altering its central carbon utilisation pathways.

Indexed as

Anti-Infective AgentsBacterial ProteinsCarbonCopperGlyceraldehyde-3-Phosphate DehydrogenasesHumansOxidative StressStaphylococcal InfectionsStaphylococcus aureusStress, PhysiologicalAnti-Infective AgentsBacterial ProteinsCarbonCopperGlyceraldehyde-3-Phosphate Dehydrogenases

Identifiers

PMID30443649
PMCPMC6350627
OpenAlexW2901531046

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.