Evidence map›Paper›PMID 26936660›Full record

ArticleScientific reports2016

Antibacterial activity and mechanism of action of auranofin against multi-drug resistant bacterial pathogens.

Shankar Thangamani, Haroon Mohammad, Mostafa F N Abushahba, Tiago J P Sobreira, Victoria E Hedrick, Lake N Paul, Mohamed N Seleem

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
21.4field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 204 citations in OpenAlex.

  1. Article
  2. Article
  3. Synergy Between the Auranofin Analogue PEtInternational journal of molecular sciences · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Anti-staphylococcal activity of the auranofin-analogous PEtFrontiers in cellular and infection microbiology · 2026
    Article
  9. Article
  10. Article
  11. Drug Repurposing: An Emerging Strategy inJournal of microbiology and biotechnology · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

43 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 2 countries.

Shankar ThangamaniDepartment of Comparative Pathobiology, Purdue University College of Veterinary Medicine, West Lafayette, IN, USA.
Haroon MohammadDepartment of Comparative Pathobiology, Purdue University College of Veterinary Medicine, West Lafayette, IN, USA.
Mostafa F N AbushahbaDepartment of Comparative Pathobiology, Purdue University College of Veterinary Medicine, West Lafayette, IN, USA.
Tiago J P SobreiraBindley Bioscience Center, Purdue University, West Lafayette, IN, USA.
Victoria E HedrickBindley Bioscience Center, Purdue University, West Lafayette, IN, USA.
Lake N PaulBindley Bioscience Center, Purdue University, West Lafayette, IN, USA.
Mohamed N SeleemDepartment of Comparative Pathobiology, Purdue University College of Veterinary Medicine, West Lafayette, IN, USA.
Purdue University West Lafayette · USAssiut University · EG

Funding

Repurposing auranofin as antimicrobial to treat staphylococcal infectionsR56AI114861 · NIAID · PURDUE UNIVERSITY · PI SELEEM, MOHAMED · 2015 to 2015
$376k
NIAID NIH HHS HHSN272200700055CNIAID NIH HHS R56 AI114861NIAID NIH HHS R56AI114861PHS HHS HHSN272200700055C
6 · The paper itself

Abstract

Traditional methods employed to discover new antibiotics are both a time-consuming and financially-taxing venture. This has led researchers to mine existing libraries of clinical molecules in order to repurpose old drugs for new applications (as antimicrobials). Such an effort led to the discovery of auranofin, a drug initially approved as an anti-rheumatic agent, which also possesses potent antibacterial activity in a clinically achievable range. The present study demonstrates auranofin's antibacterial activity is a complex process that involves inhibition of multiple biosynthetic pathways including cell wall, DNA, and bacterial protein synthesis. We also confirmed that the lack of activity of auranofin observed against Gram-negative bacteria is due to the permeability barrier conferred by the outer membrane. Auranofin's ability to suppress bacterial protein synthesis leads to significant reduction in the production of key methicillin-resistant Staphylococcus aureus (MRSA) toxins. Additionally, auranofin is capable of eradicating intracellular MRSA present inside infected macrophage cells. Furthermore, auranofin is efficacious in a mouse model of MRSA systemic infection and significantly reduces the bacterial load in murine organs including the spleen and liver. Collectively, this study provides valuable evidence that auranofin has significant promise to be repurposed as a novel antibacterial for treatment of invasive bacterial infections.

Indexed as

AnimalsAuranofinBacterial ProteinsDrug Resistance, Multiple, BacterialMethicillin-Resistant Staphylococcus aureusMiceProtein BiosynthesisStaphylococcal InfectionsAuranofinBacterial Proteins

Identifiers

PMID26936660
PMCPMC4776257
OpenAlexW2321970843

What OpenQuestion holds

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LicenceCC BY
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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.