Evidence map›Paper›PMID 28848005›Full record

ArticleAntimicrobial agents and chemotherapy2017

Induction of Mitochondrial Reactive Oxygen Species Production by Itraconazole, Terbinafine, and Amphotericin B as a Mode of Action against Aspergillus fumigatus.

Elena Shekhova, Olaf Kniemeyer, Axel A Brakhage

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

67 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  5. Frontiers in microbiology · 2026
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  6. Review
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  8. Article
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  11. The proteomic response ofmicroLife · 2025
    Article
  12. Article
  13. Shining a light on the impact of antifungals onAntimicrobial agents and chemotherapy · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

7 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

3 authors at 2 institutions in 1 country.

Elena ShekhovaDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, and Department of Microbiology and Molecular Biology, Friedrich Schiller University, Jena, Germany.
Olaf KniemeyerDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, and Department of Microbiology and Molecular Biology, Friedrich Schiller University, Jena, Germany olaf.kniemeyer@leibniz-hki.de axel.brakhage@leibniz-hki.de.
Axel A BrakhageDepartment of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute, and Department of Microbiology and Molecular Biology, Friedrich Schiller University, Jena, Germany olaf.kniemeyer@leibniz-hki.de axel.brakhage@leibniz-hki.de.
Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DEFriedrich Schiller University Jena · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug resistance in fungal pathogens is of incredible importance to global health, yet the mechanisms of drug action remain only loosely defined. Antifungal compounds have been shown to trigger the intracellular accumulation of reactive oxygen species (ROS) in human-pathogenic yeasts, but the source of those ROS remained unknown. In the present study, we examined the role of endogenous ROS for the antifungal activity of the three different antifungal substances itraconazole, terbinafine, and amphotericin B, which all target the fungal cell membrane. All three antifungals had an impact on fungal redox homeostasis by causing increased intracellular ROS production. Interestingly, the elevated ROS levels induced by antifungals were abolished by inhibition of the mitochondrial respiratory complex I with rotenone. Further, evaluation of lipid peroxidation using the thiobarbituric acid assay revealed that rotenone pretreatment decreased ROS-induced lipid peroxidation during incubation of

Indexed as

Amphotericin BAntifungal AgentsAspergillus fumigatusDrug Resistance, FungalElectron Transport Complex IItraconazoleLipid PeroxidationMitochondriaMitochondrial MembranesNaphthalenesOxidative StressReactive Oxygen SpeciesSulfhydryl CompoundsTerbinafineAmphotericin BAntifungal AgentsElectron Transport Complex IItraconazoleNaphthalenesReactive Oxygen SpeciesSulfhydryl CompoundsTerbinafineamphotericin BAspergillus fumigatusitraconazoleROSterbinafine

Identifiers

PMID28848005
PMCPMC5655112
OpenAlexW2748841886

What OpenQuestion holds

Textmetadata
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.