Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans

Autores
Peralta, Mariana Andrea; Cabrera, Jose Luis; Paraje, María Gabriela
Año de publicación
2017
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
Treatment of Candida infections is often difficult due to, between others factors, the ability of Candida species to form biofilms. These highly resistant structures exhibit resistance to a variety of antifungalagents with clinical use. Therefore, combining them with compounds obtained from natural sourcesseems to be one of the strategies in order to restore the sensitivity of the microorganism to conventional antifungals such as azole drugs. In previous works, we reported inhibitory activity ofusnic acid (UA), a natural compound obtained from lichens, against azole-resistant Candida albicansbiofilm. The biofilms inhibitory concentration (BIC) was 4 mg/ml compared to fluconazole (FLZ, BIC, 2mg/ml) with inhibitions percentages of about 70%. The present study investigated the sensitization (restoring the sensitivity of the microorganism to azoledrugs used in the clinic) of azole-resistant C. albicans biofilms to FLZ by combining it with an activecompound (UA) obtained from Argentinean native flora (Usnea amblyclada). Compound: UA was purified from the benzene extract of lichen U. amblyoclada. Microorganisms: An azole-resistant strain of C. albicans isolated from the oral cavity (RCa) that over expresses efflux transporters genes of type CDR1, CDR2 and MDR1 was used. Biofilm formation was measured by adhesion to a 96-well plate and quantified by Crystal Violet (CV) staining and spectrophotometric reading of Optical Density (OD) at 595 nm. The biofilm biomass unit(BBU) was defined as 0.1DO595nm = 1UBB. For antifungal activity determination different concentrations of UA (1 to 4 mg/ml) dissolved in dimethylsulfoxide (DMSO), FLZ (0.5 to 2 mg/ml) or their combinations were added to each well containing the mature biofilm and incubated at 37 °C for 48h. The counts of Colony Forming Units (CFU/ml) wereperformed for BBU correlation studies. Scanning Confocal Laser Microscopy (SCLM): the samples were stained with Calcofluor White (0.05%v/v). UA and FLZ combined at concentrations four-fold lower than their BICs had a greater inhibitory effecton biofilms. In fact, the combination of UA (1 mg/ml) and FLZ (0.5 mg/ml) achieved an inhibition of 79,82% while UA and FLZ combined at 1 mg/ml and 0.5 mg/ml respectively, almost eradicated de mature biofilm with an inhibition of 97.69% (* p < 0.01). Analysis by SCLM showed a considerable decrease in biomass of biofilms treated with thecombination of UA (1 mg/ml) and FLZ (0.5 mg/ml), compared to untreated RCa biofilms (* p < 0.01).These results suggest that the combination of UA with FLZ effect enhanced the activity of FLZ in thetreatment of azole-resistant of C. albicans biofilms. This promising action would imply an improvementof the therapeutics due to the decrease of the concentrations used of antifungal drugs.
Fil: Peralta, Mariana Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Cabrera, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Paraje, María Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales; Argentina
XII Congreso Argentino de Microbiología General
San Miguel de Tucumán
Argentina
Asociación Civil de Microbiología General
Materia
ANTIBIOFILM
FLUCONAZOLE
USNIC ACID
CANDIDA ALBICANS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/223759

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spelling Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicansPeralta, Mariana AndreaCabrera, Jose LuisParaje, María GabrielaANTIBIOFILMFLUCONAZOLEUSNIC ACIDCANDIDA ALBICANShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Treatment of Candida infections is often difficult due to, between others factors, the ability of Candida species to form biofilms. These highly resistant structures exhibit resistance to a variety of antifungalagents with clinical use. Therefore, combining them with compounds obtained from natural sourcesseems to be one of the strategies in order to restore the sensitivity of the microorganism to conventional antifungals such as azole drugs. In previous works, we reported inhibitory activity ofusnic acid (UA), a natural compound obtained from lichens, against azole-resistant Candida albicansbiofilm. The biofilms inhibitory concentration (BIC) was 4 mg/ml compared to fluconazole (FLZ, BIC, 2mg/ml) with inhibitions percentages of about 70%. The present study investigated the sensitization (restoring the sensitivity of the microorganism to azoledrugs used in the clinic) of azole-resistant C. albicans biofilms to FLZ by combining it with an activecompound (UA) obtained from Argentinean native flora (Usnea amblyclada). Compound: UA was purified from the benzene extract of lichen U. amblyoclada. Microorganisms: An azole-resistant strain of C. albicans isolated from the oral cavity (RCa) that over expresses efflux transporters genes of type CDR1, CDR2 and MDR1 was used. Biofilm formation was measured by adhesion to a 96-well plate and quantified by Crystal Violet (CV) staining and spectrophotometric reading of Optical Density (OD) at 595 nm. The biofilm biomass unit(BBU) was defined as 0.1DO595nm = 1UBB. For antifungal activity determination different concentrations of UA (1 to 4 mg/ml) dissolved in dimethylsulfoxide (DMSO), FLZ (0.5 to 2 mg/ml) or their combinations were added to each well containing the mature biofilm and incubated at 37 °C for 48h. The counts of Colony Forming Units (CFU/ml) wereperformed for BBU correlation studies. Scanning Confocal Laser Microscopy (SCLM): the samples were stained with Calcofluor White (0.05%v/v). UA and FLZ combined at concentrations four-fold lower than their BICs had a greater inhibitory effecton biofilms. In fact, the combination of UA (1 mg/ml) and FLZ (0.5 mg/ml) achieved an inhibition of 79,82% while UA and FLZ combined at 1 mg/ml and 0.5 mg/ml respectively, almost eradicated de mature biofilm with an inhibition of 97.69% (* p < 0.01). Analysis by SCLM showed a considerable decrease in biomass of biofilms treated with thecombination of UA (1 mg/ml) and FLZ (0.5 mg/ml), compared to untreated RCa biofilms (* p < 0.01).These results suggest that the combination of UA with FLZ effect enhanced the activity of FLZ in thetreatment of azole-resistant of C. albicans biofilms. This promising action would imply an improvementof the therapeutics due to the decrease of the concentrations used of antifungal drugs.Fil: Peralta, Mariana Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Cabrera, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; ArgentinaFil: Paraje, María Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales; ArgentinaXII Congreso Argentino de Microbiología GeneralSan Miguel de TucumánArgentinaAsociación Civil de Microbiología GeneralAsociación Civil de Microbiología General2017info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/223759Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans; XII Congreso Argentino de Microbiología General; San Miguel de Tucumán; Argentina; 2017; 150-150CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://samige.org.ar/wp-content/uploads/2022/10/Libro-SAMIGE-2017.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:12:03Zoai:ri.conicet.gov.ar:11336/223759instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:12:03.451CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
title Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
spellingShingle Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
Peralta, Mariana Andrea
ANTIBIOFILM
FLUCONAZOLE
USNIC ACID
CANDIDA ALBICANS
title_short Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
title_full Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
title_fullStr Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
title_full_unstemmed Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
title_sort Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans
dc.creator.none.fl_str_mv Peralta, Mariana Andrea
Cabrera, Jose Luis
Paraje, María Gabriela
author Peralta, Mariana Andrea
author_facet Peralta, Mariana Andrea
Cabrera, Jose Luis
Paraje, María Gabriela
author_role author
author2 Cabrera, Jose Luis
Paraje, María Gabriela
author2_role author
author
dc.subject.none.fl_str_mv ANTIBIOFILM
FLUCONAZOLE
USNIC ACID
CANDIDA ALBICANS
topic ANTIBIOFILM
FLUCONAZOLE
USNIC ACID
CANDIDA ALBICANS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Treatment of Candida infections is often difficult due to, between others factors, the ability of Candida species to form biofilms. These highly resistant structures exhibit resistance to a variety of antifungalagents with clinical use. Therefore, combining them with compounds obtained from natural sourcesseems to be one of the strategies in order to restore the sensitivity of the microorganism to conventional antifungals such as azole drugs. In previous works, we reported inhibitory activity ofusnic acid (UA), a natural compound obtained from lichens, against azole-resistant Candida albicansbiofilm. The biofilms inhibitory concentration (BIC) was 4 mg/ml compared to fluconazole (FLZ, BIC, 2mg/ml) with inhibitions percentages of about 70%. The present study investigated the sensitization (restoring the sensitivity of the microorganism to azoledrugs used in the clinic) of azole-resistant C. albicans biofilms to FLZ by combining it with an activecompound (UA) obtained from Argentinean native flora (Usnea amblyclada). Compound: UA was purified from the benzene extract of lichen U. amblyoclada. Microorganisms: An azole-resistant strain of C. albicans isolated from the oral cavity (RCa) that over expresses efflux transporters genes of type CDR1, CDR2 and MDR1 was used. Biofilm formation was measured by adhesion to a 96-well plate and quantified by Crystal Violet (CV) staining and spectrophotometric reading of Optical Density (OD) at 595 nm. The biofilm biomass unit(BBU) was defined as 0.1DO595nm = 1UBB. For antifungal activity determination different concentrations of UA (1 to 4 mg/ml) dissolved in dimethylsulfoxide (DMSO), FLZ (0.5 to 2 mg/ml) or their combinations were added to each well containing the mature biofilm and incubated at 37 °C for 48h. The counts of Colony Forming Units (CFU/ml) wereperformed for BBU correlation studies. Scanning Confocal Laser Microscopy (SCLM): the samples were stained with Calcofluor White (0.05%v/v). UA and FLZ combined at concentrations four-fold lower than their BICs had a greater inhibitory effecton biofilms. In fact, the combination of UA (1 mg/ml) and FLZ (0.5 mg/ml) achieved an inhibition of 79,82% while UA and FLZ combined at 1 mg/ml and 0.5 mg/ml respectively, almost eradicated de mature biofilm with an inhibition of 97.69% (* p < 0.01). Analysis by SCLM showed a considerable decrease in biomass of biofilms treated with thecombination of UA (1 mg/ml) and FLZ (0.5 mg/ml), compared to untreated RCa biofilms (* p < 0.01).These results suggest that the combination of UA with FLZ effect enhanced the activity of FLZ in thetreatment of azole-resistant of C. albicans biofilms. This promising action would imply an improvementof the therapeutics due to the decrease of the concentrations used of antifungal drugs.
Fil: Peralta, Mariana Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Cabrera, Jose Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina
Fil: Paraje, María Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales; Argentina
XII Congreso Argentino de Microbiología General
San Miguel de Tucumán
Argentina
Asociación Civil de Microbiología General
description Treatment of Candida infections is often difficult due to, between others factors, the ability of Candida species to form biofilms. These highly resistant structures exhibit resistance to a variety of antifungalagents with clinical use. Therefore, combining them with compounds obtained from natural sourcesseems to be one of the strategies in order to restore the sensitivity of the microorganism to conventional antifungals such as azole drugs. In previous works, we reported inhibitory activity ofusnic acid (UA), a natural compound obtained from lichens, against azole-resistant Candida albicansbiofilm. The biofilms inhibitory concentration (BIC) was 4 mg/ml compared to fluconazole (FLZ, BIC, 2mg/ml) with inhibitions percentages of about 70%. The present study investigated the sensitization (restoring the sensitivity of the microorganism to azoledrugs used in the clinic) of azole-resistant C. albicans biofilms to FLZ by combining it with an activecompound (UA) obtained from Argentinean native flora (Usnea amblyclada). Compound: UA was purified from the benzene extract of lichen U. amblyoclada. Microorganisms: An azole-resistant strain of C. albicans isolated from the oral cavity (RCa) that over expresses efflux transporters genes of type CDR1, CDR2 and MDR1 was used. Biofilm formation was measured by adhesion to a 96-well plate and quantified by Crystal Violet (CV) staining and spectrophotometric reading of Optical Density (OD) at 595 nm. The biofilm biomass unit(BBU) was defined as 0.1DO595nm = 1UBB. For antifungal activity determination different concentrations of UA (1 to 4 mg/ml) dissolved in dimethylsulfoxide (DMSO), FLZ (0.5 to 2 mg/ml) or their combinations were added to each well containing the mature biofilm and incubated at 37 °C for 48h. The counts of Colony Forming Units (CFU/ml) wereperformed for BBU correlation studies. Scanning Confocal Laser Microscopy (SCLM): the samples were stained with Calcofluor White (0.05%v/v). UA and FLZ combined at concentrations four-fold lower than their BICs had a greater inhibitory effecton biofilms. In fact, the combination of UA (1 mg/ml) and FLZ (0.5 mg/ml) achieved an inhibition of 79,82% while UA and FLZ combined at 1 mg/ml and 0.5 mg/ml respectively, almost eradicated de mature biofilm with an inhibition of 97.69% (* p < 0.01). Analysis by SCLM showed a considerable decrease in biomass of biofilms treated with thecombination of UA (1 mg/ml) and FLZ (0.5 mg/ml), compared to untreated RCa biofilms (* p < 0.01).These results suggest that the combination of UA with FLZ effect enhanced the activity of FLZ in thetreatment of azole-resistant of C. albicans biofilms. This promising action would imply an improvementof the therapeutics due to the decrease of the concentrations used of antifungal drugs.
publishDate 2017
dc.date.none.fl_str_mv 2017
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dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/223759
Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans; XII Congreso Argentino de Microbiología General; San Miguel de Tucumán; Argentina; 2017; 150-150
CONICET Digital
CONICET
url http://hdl.handle.net/11336/223759
identifier_str_mv Antibiofilm combination of usnic acid with fluconazole on resistant Candida albicans; XII Congreso Argentino de Microbiología General; San Miguel de Tucumán; Argentina; 2017; 150-150
CONICET Digital
CONICET
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