Cited by 113Antifungal resistance and susceptibilityFungal and yeast genetics researchFungal Infections and Studies

Role of cell defense against oxidative damage in the resistance of Candida albicans to the killing effect of amphotericin B

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Sokol-Anderson, M, Sligh, J E, Elberg, S, Brajtburg, J, Kobayashi, G S, Medoff, G·1988·Antimicrobial Agents and Chemotherapy

Abstract

A laboratory-derived mutant of Candida albicans B311 (L) and a clinical isolate (C) of C. albicans, both lacking membrane ergosterol, were less susceptible to amphotericin B (AmB)-induced cell membrane permeability to K+ and lethality than was the wild-type laboratory strain (B311) which contained ergosterol. The resistance of L and C to AmB-induced killing was much greater than the level of resistance to AmB-induced cell membrane permeability. L and C were also less susceptible to killing by H2O2 than was B311, and when treated with menadione, they each produced less H2O2 than did B311. In addition, their levels of catalase activity were 3.8-fold (L) and 2-fold (C) higher than that of B311. The ergosterol deficiency in L and C probably impaired AmB binding to the cells, thereby lowering AmB effectiveness as measured by both cell membrane permeability and killing. Resistance of strains L and C to oxidation-dependent damage likely contributed to a diminished response to AmB-induced lethality.

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Crossref · 10.1128/aac.32.5.702

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Authors
Sokol-Anderson, M., Sligh, J. E., Elberg, S., Brajtburg, J., Kobayashi, G. S., & Medoff, G.
Affiliations
Washington University in St. Louis (US)
Venue
Antimicrobial Agents and Chemotherapy
Published
1988-05
Volume
32
Issue
5
Pages
702-705
ISSN
  • 0066-4804 (ISSN-L)
  • 1098-6596
OpenAlex
W2069801130
Cited by
113
References
16
Citations by year
2026: 1 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 4 · 2018: 2 · 2017: 7 · 2016: 4 · 2015: 3 · 2014: 2 · 2013: 4 · 2012: 4
FWCI
1.62
Type
journal article
Language
en
Open access
Locations
  • Antimicrobial Agents and Chemotherapy (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of Allergy and Infectious Diseases (AI 07172, AI 07015, AI-16228)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
Keywords
Candida albicans, amphotericin B resistance, oxidative stress, cell membrane permeability, hydrogen peroxide, menadione, catalase activity, antifungal resistance, cell membrane damage
MeSH terms
Amphotericin B, Candida albicans, Catalase, Cell Membrane, Cell Membrane Permeability, Drug Resistance, Microbial, Ergosterol, Humans, Hydrogen Peroxide, Oxidation-Reduction

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