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Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans
The fungal cell wall and membrane are the principal targets of antifungals. Herein, we report that myricetin exerts antifungal activity against Candida albicans by damaging the cell wall integrity and notably enhancing the membrane permeability. In the presence of sorbitol, an osmotic protectant, th...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Microbiology and Biotechnology
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628827/ https://www.ncbi.nlm.nih.gov/pubmed/34750288 http://dx.doi.org/10.4014/jmb.2110.10014 |
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author | Lee, Heung-Shick Kim, Younhee |
author_facet | Lee, Heung-Shick Kim, Younhee |
author_sort | Lee, Heung-Shick |
collection | PubMed |
description | The fungal cell wall and membrane are the principal targets of antifungals. Herein, we report that myricetin exerts antifungal activity against Candida albicans by damaging the cell wall integrity and notably enhancing the membrane permeability. In the presence of sorbitol, an osmotic protectant, the minimum inhibitory concentration (MIC) of myricetin against C. albicans increased from 20 to 40 and 80 μg/ml in 24 and 72 h, respectively, demonstrating that myricetin disturbs the cell wall integrity of C. albicans. Fluorescence microscopic images showed the presence of propidium iodidestained C. albicans cells, indicating the myricetin-induced initial damage of the cell membrane. The effects of myricetin on the membrane permeability of C. albicans cells were assessed using crystal violet-uptake and intracellular material-leakage assays. The percentage uptakes of crystal violet for myricetin-treated C. albicans cells at 1×, 2×, and 4× the MIC of myricetin were 36.5, 60.6, and 79.4%, respectively, while those for DMSO-treated C. albicans cells were 28.2, 28.9, and 29.7%, respectively. Additionally, myricetin-treated C. albicans cells showed notable DNA and protein leakage, compared with the DMSO-treated controls. Furthermore, treatment of C. albicans cells with 1× the MIC of myricetin showed a 17.2 and 28.0% reduction in the binding of the lipophilic probes diphenylhexatriene and Nile red, respectively, indicating that myricetin alters the lipid components or order in the C. albicans cell membrane, leading to increased membrane permeability. Therefore, these data will provide insights into the pharmacological worth of myricetin as a prospective antifungal for treating C. albicans infections. |
format | Online Article Text |
id | pubmed-9628827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society for Microbiology and Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96288272022-12-13 Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans Lee, Heung-Shick Kim, Younhee J Microbiol Biotechnol Research article The fungal cell wall and membrane are the principal targets of antifungals. Herein, we report that myricetin exerts antifungal activity against Candida albicans by damaging the cell wall integrity and notably enhancing the membrane permeability. In the presence of sorbitol, an osmotic protectant, the minimum inhibitory concentration (MIC) of myricetin against C. albicans increased from 20 to 40 and 80 μg/ml in 24 and 72 h, respectively, demonstrating that myricetin disturbs the cell wall integrity of C. albicans. Fluorescence microscopic images showed the presence of propidium iodidestained C. albicans cells, indicating the myricetin-induced initial damage of the cell membrane. The effects of myricetin on the membrane permeability of C. albicans cells were assessed using crystal violet-uptake and intracellular material-leakage assays. The percentage uptakes of crystal violet for myricetin-treated C. albicans cells at 1×, 2×, and 4× the MIC of myricetin were 36.5, 60.6, and 79.4%, respectively, while those for DMSO-treated C. albicans cells were 28.2, 28.9, and 29.7%, respectively. Additionally, myricetin-treated C. albicans cells showed notable DNA and protein leakage, compared with the DMSO-treated controls. Furthermore, treatment of C. albicans cells with 1× the MIC of myricetin showed a 17.2 and 28.0% reduction in the binding of the lipophilic probes diphenylhexatriene and Nile red, respectively, indicating that myricetin alters the lipid components or order in the C. albicans cell membrane, leading to increased membrane permeability. Therefore, these data will provide insights into the pharmacological worth of myricetin as a prospective antifungal for treating C. albicans infections. The Korean Society for Microbiology and Biotechnology 2022-01-28 2021-10-30 /pmc/articles/PMC9628827/ /pubmed/34750288 http://dx.doi.org/10.4014/jmb.2110.10014 Text en Copyright © 2022 by the authors. Licensee KMB. https://creativecommons.org/licenses/by/4.0/This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research article Lee, Heung-Shick Kim, Younhee Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title | Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title_full | Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title_fullStr | Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title_full_unstemmed | Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title_short | Myricetin Disturbs the Cell Wall Integrity and Increases the Membrane Permeability of Candida albicans |
title_sort | myricetin disturbs the cell wall integrity and increases the membrane permeability of candida albicans |
topic | Research article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9628827/ https://www.ncbi.nlm.nih.gov/pubmed/34750288 http://dx.doi.org/10.4014/jmb.2110.10014 |
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