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Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway

Amphotericin B (AmB) induces oxidative and nitrosative stresses, characterized by production of reactive oxygen and nitrogen species, in fungi. Yet, how these toxic species contribute to AmB-induced fungal cell death is unclear. We investigated the role of superoxide and nitric oxide radicals in AmB...

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Autores principales: Vriens, Kim, Kumar, Phalguni Tewari, Struyfs, Caroline, Cools, Tanne L., Spincemaille, Pieter, Kokalj, Tadej, Sampaio-Marques, Belém, Ludovico, Paula, Lammertyn, Jeroen, Cammue, Bruno P. A., Thevissen, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654257/
https://www.ncbi.nlm.nih.gov/pubmed/29129987
http://dx.doi.org/10.1155/2017/4064628
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author Vriens, Kim
Kumar, Phalguni Tewari
Struyfs, Caroline
Cools, Tanne L.
Spincemaille, Pieter
Kokalj, Tadej
Sampaio-Marques, Belém
Ludovico, Paula
Lammertyn, Jeroen
Cammue, Bruno P. A.
Thevissen, Karin
author_facet Vriens, Kim
Kumar, Phalguni Tewari
Struyfs, Caroline
Cools, Tanne L.
Spincemaille, Pieter
Kokalj, Tadej
Sampaio-Marques, Belém
Ludovico, Paula
Lammertyn, Jeroen
Cammue, Bruno P. A.
Thevissen, Karin
author_sort Vriens, Kim
collection PubMed
description Amphotericin B (AmB) induces oxidative and nitrosative stresses, characterized by production of reactive oxygen and nitrogen species, in fungi. Yet, how these toxic species contribute to AmB-induced fungal cell death is unclear. We investigated the role of superoxide and nitric oxide radicals in AmB's fungicidal activity in Saccharomyces cerevisiae, using a digital microfluidic platform, which enabled monitoring individual cells at a spatiotemporal resolution, and plating assays. The nitric oxide synthase inhibitor L-NAME was used to interfere with nitric oxide radical production. L-NAME increased and accelerated AmB-induced accumulation of superoxide radicals, membrane permeabilization, and loss of proliferative capacity in S. cerevisiae. In contrast, the nitric oxide donor S-nitrosoglutathione inhibited AmB's action. Hence, superoxide radicals were important for AmB's fungicidal action, whereas nitric oxide radicals mediated tolerance towards AmB. Finally, also the human pathogens Candida albicans and Candida glabrata were more susceptible to AmB in the presence of L-NAME, pointing to the potential of AmB-L-NAME combination therapy to treat fungal infections.
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spelling pubmed-56542572017-11-12 Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway Vriens, Kim Kumar, Phalguni Tewari Struyfs, Caroline Cools, Tanne L. Spincemaille, Pieter Kokalj, Tadej Sampaio-Marques, Belém Ludovico, Paula Lammertyn, Jeroen Cammue, Bruno P. A. Thevissen, Karin Oxid Med Cell Longev Research Article Amphotericin B (AmB) induces oxidative and nitrosative stresses, characterized by production of reactive oxygen and nitrogen species, in fungi. Yet, how these toxic species contribute to AmB-induced fungal cell death is unclear. We investigated the role of superoxide and nitric oxide radicals in AmB's fungicidal activity in Saccharomyces cerevisiae, using a digital microfluidic platform, which enabled monitoring individual cells at a spatiotemporal resolution, and plating assays. The nitric oxide synthase inhibitor L-NAME was used to interfere with nitric oxide radical production. L-NAME increased and accelerated AmB-induced accumulation of superoxide radicals, membrane permeabilization, and loss of proliferative capacity in S. cerevisiae. In contrast, the nitric oxide donor S-nitrosoglutathione inhibited AmB's action. Hence, superoxide radicals were important for AmB's fungicidal action, whereas nitric oxide radicals mediated tolerance towards AmB. Finally, also the human pathogens Candida albicans and Candida glabrata were more susceptible to AmB in the presence of L-NAME, pointing to the potential of AmB-L-NAME combination therapy to treat fungal infections. Hindawi 2017 2017-10-10 /pmc/articles/PMC5654257/ /pubmed/29129987 http://dx.doi.org/10.1155/2017/4064628 Text en Copyright © 2017 Kim Vriens et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Vriens, Kim
Kumar, Phalguni Tewari
Struyfs, Caroline
Cools, Tanne L.
Spincemaille, Pieter
Kokalj, Tadej
Sampaio-Marques, Belém
Ludovico, Paula
Lammertyn, Jeroen
Cammue, Bruno P. A.
Thevissen, Karin
Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title_full Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title_fullStr Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title_full_unstemmed Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title_short Increasing the Fungicidal Action of Amphotericin B by Inhibiting the Nitric Oxide-Dependent Tolerance Pathway
title_sort increasing the fungicidal action of amphotericin b by inhibiting the nitric oxide-dependent tolerance pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654257/
https://www.ncbi.nlm.nih.gov/pubmed/29129987
http://dx.doi.org/10.1155/2017/4064628
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