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Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans

The opportunistic human fungal pathogen Candida albicans relies on cell morphological transitions to develop biofilm and invade the host. In the current study, we developed new regulatory molecules, which inhibit the morphological transition of C. albicans from yeast-form cells to cells forming hyph...

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Autores principales: Ishchuk, Olena P., Sterner, Olov, Ellervik, Ulf, Manner, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167926/
https://www.ncbi.nlm.nih.gov/pubmed/31905828
http://dx.doi.org/10.3390/antibiotics9010010
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author Ishchuk, Olena P.
Sterner, Olov
Ellervik, Ulf
Manner, Sophie
author_facet Ishchuk, Olena P.
Sterner, Olov
Ellervik, Ulf
Manner, Sophie
author_sort Ishchuk, Olena P.
collection PubMed
description The opportunistic human fungal pathogen Candida albicans relies on cell morphological transitions to develop biofilm and invade the host. In the current study, we developed new regulatory molecules, which inhibit the morphological transition of C. albicans from yeast-form cells to cells forming hyphae. These compounds, benzyl α-l-fucopyranoside and benzyl β-d-xylopyranoside, inhibit the hyphae formation and adhesion of C. albicans to a polystyrene surface, resulting in a reduced biofilm formation. The addition of cAMP to cells treated with α-l-fucopyranoside restored the yeast-hyphae switch and the biofilm level to that of the untreated control. In the β-d-xylopyranoside treated cells, the biofilm level was only partially restored by the addition of cAMP, and these cells remained mainly as yeast-form cells.
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spelling pubmed-71679262020-04-21 Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans Ishchuk, Olena P. Sterner, Olov Ellervik, Ulf Manner, Sophie Antibiotics (Basel) Article The opportunistic human fungal pathogen Candida albicans relies on cell morphological transitions to develop biofilm and invade the host. In the current study, we developed new regulatory molecules, which inhibit the morphological transition of C. albicans from yeast-form cells to cells forming hyphae. These compounds, benzyl α-l-fucopyranoside and benzyl β-d-xylopyranoside, inhibit the hyphae formation and adhesion of C. albicans to a polystyrene surface, resulting in a reduced biofilm formation. The addition of cAMP to cells treated with α-l-fucopyranoside restored the yeast-hyphae switch and the biofilm level to that of the untreated control. In the β-d-xylopyranoside treated cells, the biofilm level was only partially restored by the addition of cAMP, and these cells remained mainly as yeast-form cells. MDPI 2019-12-30 /pmc/articles/PMC7167926/ /pubmed/31905828 http://dx.doi.org/10.3390/antibiotics9010010 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ishchuk, Olena P.
Sterner, Olov
Ellervik, Ulf
Manner, Sophie
Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title_full Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title_fullStr Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title_full_unstemmed Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title_short Simple Carbohydrate Derivatives Diminish the Formation of Biofilm of the Pathogenic Yeast Candida albicans
title_sort simple carbohydrate derivatives diminish the formation of biofilm of the pathogenic yeast candida albicans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7167926/
https://www.ncbi.nlm.nih.gov/pubmed/31905828
http://dx.doi.org/10.3390/antibiotics9010010
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