4.7 Article

The Production of Reactive Oxygen Species Is a Universal Action Mechanism of Amphotericin B against Pathogenic Yeasts and Contributes to the Fungicidal Effect of This Drug

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 58, Issue 11, Pages 6627-6638

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.03570-14

Keywords

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Funding

  1. Gilead
  2. Fundacion Carolina
  3. Instituto de Salud Carlos III
  4. Spanish Ministry for Economics and Competitivity [SAF2011-25140]
  5. Astellas Pharma
  6. bioMerieux
  7. Gilead Sciences
  8. Merck Sharp
  9. Dohme
  10. Pfizer
  11. Schering-Plough
  12. Soria Melguizo SA
  13. Ferrer International
  14. European Union
  15. ALBAN program
  16. Spanish Agency for International Cooperation
  17. Spanish Ministry of Culture and Education
  18. Spanish Health Research Fund
  19. Ramon Areces Foundation
  20. Mutua Madrilena Foundation

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Amphotericin B (AMB) is an antifungal drug that binds to ergosterol and forms pores at the cell membrane, causing the loss of ions. In addition, AMB induces the accumulation of reactive oxygen species (ROS), and although these molecules have multiple deleterious effects on fungal cells, their specific role in the action mechanism of AMB remains unknown. In this work, we studied the role of ROS in the action mechanism of AMB. We determined the intracellular induction of ROS in 44 isolates of different pathogenic yeast species (Candida albicans, Candida parapsilosis, Candida glabrata, Candida tropicalis, Candida krusei, Cryptococcus neoformans, and Cryptococcus gattii). We also characterized the production of ROS in AMB-resistant isolates. We found that AMB induces the formation of ROS in all the species tested. The inhibition of the mitochondrial respiratory chain by rotenone blocked the induction of ROS by AMB and provided protection from the killing action of the antifungal. Moreover, this phenomenon was absent in strains that displayed resistance to AMB. These strains showed an alteration in the respiration rate and mitochondrial membrane potential and also had higher catalase activity than that of the AMB-susceptible strains. Consistently, AMB failed to induce protein carbonylation in the resistant strains. Our data demonstrate that the production of ROS by AMB is a universal and important action mechanism that is correlated with the fungicidal effect and might explain the low rate of resistance to the molecule. Finally, these data provide an opportunity to design new strategies to improve the efficacy of this antifungal.

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