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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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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. |
format | Online Article Text |
id | pubmed-5654257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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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