Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro

Current treatments for Candida albicans infection are limited due to the limited number of antifungal drugs available and the increase in antifungal resistance. Curcumin is used as a spice, food preservative, flavoring, and coloring agent that has been shown to have many pharmacological activities....

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Main Authors: Emily Chen, Bruna Benso, Dalia Seleem, Luiz Eduardo Nunes Ferreira, Silvana Pasetto, Vanessa Pardi, Ramiro Mendonça Murata
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:International Journal of Dentistry
Online Access:http://dx.doi.org/10.1155/2018/2393146
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author Emily Chen
Bruna Benso
Dalia Seleem
Luiz Eduardo Nunes Ferreira
Silvana Pasetto
Vanessa Pardi
Ramiro Mendonça Murata
author_facet Emily Chen
Bruna Benso
Dalia Seleem
Luiz Eduardo Nunes Ferreira
Silvana Pasetto
Vanessa Pardi
Ramiro Mendonça Murata
author_sort Emily Chen
collection DOAJ
description Current treatments for Candida albicans infection are limited due to the limited number of antifungal drugs available and the increase in antifungal resistance. Curcumin is used as a spice, food preservative, flavoring, and coloring agent that has been shown to have many pharmacological activities. Thus, this study evaluated the modulatory effects of curcumin on major virulence factors associated with the pathogenicity of C. albicans. The minimum inhibitory concentration (MIC) of curcumin against C. albicans (SC5314) was determined. Biofilm formation was quantified and the proteinase and phospholipase secretion was measured. The cytotoxicity was tested in oral fibroblast cells. A cocultured model was used to analyze the gene expression of proinflammatory cytokines (IL-1β, IL-1α, and IL-6) from host cells, as well SAP-1 and PLB-1 by RT-PCR. The MIC was between 6.25 and 12.5 µM, and the activity of proteinase enzyme was significantly decreased in biofilms treated with curcumin. However, proteinase gene expression was not downregulated after curcumin treatment. Furthermore, gene expressions of host inflammatory response, IL-1β and IL-1α, were significantly downregulated after exposure to curcumin. In conclusion, curcumin exhibited antifungal activity against C. albicans and modulated the proteolytic enzyme activities without downregulating the gene expression. In host inflammatory response, curcumin downregulated IL-1β and IL-1α gene expression.
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spelling doaj-art-91e7f7df3fb64979b325381ee67bfb382025-02-03T01:12:57ZengWileyInternational Journal of Dentistry1687-87281687-87362018-01-01201810.1155/2018/23931462393146Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In VitroEmily Chen0Bruna Benso1Dalia Seleem2Luiz Eduardo Nunes Ferreira3Silvana Pasetto4Vanessa Pardi5Ramiro Mendonça Murata6Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USASchool of Dentistry, Pontificia Universidad Católica de Chile, Santiago, ChileCollege of Dental Medicine, Western University of Health Sciences, Pomona, CA, USASchool of Dental Medicine, East Carolina University, Greenville, NC, USAHerman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USAHerman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USASchool of Dental Medicine, East Carolina University, Greenville, NC, USACurrent treatments for Candida albicans infection are limited due to the limited number of antifungal drugs available and the increase in antifungal resistance. Curcumin is used as a spice, food preservative, flavoring, and coloring agent that has been shown to have many pharmacological activities. Thus, this study evaluated the modulatory effects of curcumin on major virulence factors associated with the pathogenicity of C. albicans. The minimum inhibitory concentration (MIC) of curcumin against C. albicans (SC5314) was determined. Biofilm formation was quantified and the proteinase and phospholipase secretion was measured. The cytotoxicity was tested in oral fibroblast cells. A cocultured model was used to analyze the gene expression of proinflammatory cytokines (IL-1β, IL-1α, and IL-6) from host cells, as well SAP-1 and PLB-1 by RT-PCR. The MIC was between 6.25 and 12.5 µM, and the activity of proteinase enzyme was significantly decreased in biofilms treated with curcumin. However, proteinase gene expression was not downregulated after curcumin treatment. Furthermore, gene expressions of host inflammatory response, IL-1β and IL-1α, were significantly downregulated after exposure to curcumin. In conclusion, curcumin exhibited antifungal activity against C. albicans and modulated the proteolytic enzyme activities without downregulating the gene expression. In host inflammatory response, curcumin downregulated IL-1β and IL-1α gene expression.http://dx.doi.org/10.1155/2018/2393146
spellingShingle Emily Chen
Bruna Benso
Dalia Seleem
Luiz Eduardo Nunes Ferreira
Silvana Pasetto
Vanessa Pardi
Ramiro Mendonça Murata
Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
International Journal of Dentistry
title Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
title_full Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
title_fullStr Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
title_full_unstemmed Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
title_short Fungal-Host Interaction: Curcumin Modulates Proteolytic Enzyme Activity of Candida albicans and Inflammatory Host Response In Vitro
title_sort fungal host interaction curcumin modulates proteolytic enzyme activity of candida albicans and inflammatory host response in vitro
url http://dx.doi.org/10.1155/2018/2393146
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