2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms

Detalhes bibliográficos
Autor(a) principal: Bila, Níura Madalena [UNESP]
Data de Publicação: 2021
Outros Autores: Costa-Orlandi, Caroline Barcelos [UNESP], Vaso, Carolina Orlando [UNESP], Bonatti, Jean Lucas Carvalho [UNESP], de Assis, Letícia Ribeiro [UNESP], Regasini, Luís Octavio [UNESP], Fontana, Carla Raquel [UNESP], Fusco-Almeida, Ana Marisa [UNESP], Mendes-Giannini, Maria José Soares [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3389/fcimb.2021.679470
http://hdl.handle.net/11449/207825
Resumo: Dermatophytes, fungi that cause dermatophytosis, can invade keratinized tissues in humans and animals. The biofilm-forming ability of these fungi was described recently, and it may be correlated with the long treatment period and common recurrences of this mycosis. In this study, we evaluated the anti-dermatophytic and anti-biofilm activity of 2-hydroxychalcone (2-chalcone) in the dark and photodynamic therapy (PDT)-mediated and to determine its mechanism of action. Trichophyton rubrum and Trichophyton mentagrophytes strains were used in the study. The antifungal susceptibility test of planktonic cells, early-stage biofilms, and mature biofilms were performed using colorimetric methods. Topographies were visualized by scanning electron microscopy (SEM). Human skin keratinocyte (HaCat) monolayers were also used in the cytotoxicity assays. The mechanisms of action of 2-chalcone in the dark and under photoexcitation were investigated using confocal microscopy and the quantification of ergosterol, reactive oxygen species (ROS), and death induction by apoptosis/necrosis. All strains, in the planktonic form, were inhibited after treatment with 2-chalcone (minimum inhibitory concentration (MIC) = 7.8-15.6 mg/L), terbinafine (TRB) (MIC = 0.008–0.03 mg/L), and fluconazole (FLZ) (1–512 mg/L). Early-stage biofilm and mature biofilms were inhibited by 2-chalcone at concentrations of 15.6 mg/L and 31.2 mg/L in all tested strains. However, mature biofilms were resistant to all the antifungal drugs tested. When planktonic cells and biofilms (early-stage and mature) were treated with 2-chalcone-mediated PDT, the inhibitory concentrations were reduced by four times (2–7.8 mg/L). SEM images of biofilms treated with 2-chalcone showed cell wall collapse, resulting from a probable extravasation of cytoplasmic content. The toxicity of 2-chalcone in HaCat cells showed higher IC50 values in the dark than under photoexcitation. Further, 2-chalcone targets ergosterol in the cell and promotes the generation of ROS, resulting in cell death by apoptosis and necrosis. Overall, 2-chalcone-mediated PDT is a promising and safe drug candidate against dermatophytes, particularly in anti-biofilm treatment.
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spelling 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms2-chalconebiofilmsdermatophytesmechanism of actionphotodynamic therapyT. mentagrophytesTrichophyton rubrumDermatophytes, fungi that cause dermatophytosis, can invade keratinized tissues in humans and animals. The biofilm-forming ability of these fungi was described recently, and it may be correlated with the long treatment period and common recurrences of this mycosis. In this study, we evaluated the anti-dermatophytic and anti-biofilm activity of 2-hydroxychalcone (2-chalcone) in the dark and photodynamic therapy (PDT)-mediated and to determine its mechanism of action. Trichophyton rubrum and Trichophyton mentagrophytes strains were used in the study. The antifungal susceptibility test of planktonic cells, early-stage biofilms, and mature biofilms were performed using colorimetric methods. Topographies were visualized by scanning electron microscopy (SEM). Human skin keratinocyte (HaCat) monolayers were also used in the cytotoxicity assays. The mechanisms of action of 2-chalcone in the dark and under photoexcitation were investigated using confocal microscopy and the quantification of ergosterol, reactive oxygen species (ROS), and death induction by apoptosis/necrosis. All strains, in the planktonic form, were inhibited after treatment with 2-chalcone (minimum inhibitory concentration (MIC) = 7.8-15.6 mg/L), terbinafine (TRB) (MIC = 0.008–0.03 mg/L), and fluconazole (FLZ) (1–512 mg/L). Early-stage biofilm and mature biofilms were inhibited by 2-chalcone at concentrations of 15.6 mg/L and 31.2 mg/L in all tested strains. However, mature biofilms were resistant to all the antifungal drugs tested. When planktonic cells and biofilms (early-stage and mature) were treated with 2-chalcone-mediated PDT, the inhibitory concentrations were reduced by four times (2–7.8 mg/L). SEM images of biofilms treated with 2-chalcone showed cell wall collapse, resulting from a probable extravasation of cytoplasmic content. The toxicity of 2-chalcone in HaCat cells showed higher IC50 values in the dark than under photoexcitation. Further, 2-chalcone targets ergosterol in the cell and promotes the generation of ROS, resulting in cell death by apoptosis and necrosis. Overall, 2-chalcone-mediated PDT is a promising and safe drug candidate against dermatophytes, particularly in anti-biofilm treatment.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Clinical Analysis School of Pharmaceutical Sciences Universidade Estadual Paulista (UNESP)Department of Para-Clinic School of Veterinary Universidade Eduardo Mondlane (UEM)Department of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences Universidade Estadual Paulista (UNESP)Department of Clinical Analysis School of Pharmaceutical Sciences Universidade Estadual Paulista (UNESP)Department of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences Universidade Estadual Paulista (UNESP)FAPESP: 2017/18388-6FAPESP: 2018/02785-9FAPESP: 2019/22188-8Universidade Estadual Paulista (Unesp)Universidade Estadual de Maringá (UEM)Bila, Níura Madalena [UNESP]Costa-Orlandi, Caroline Barcelos [UNESP]Vaso, Carolina Orlando [UNESP]Bonatti, Jean Lucas Carvalho [UNESP]de Assis, Letícia Ribeiro [UNESP]Regasini, Luís Octavio [UNESP]Fontana, Carla Raquel [UNESP]Fusco-Almeida, Ana Marisa [UNESP]Mendes-Giannini, Maria José Soares [UNESP]2021-06-25T11:01:38Z2021-06-25T11:01:38Z2021-05-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3389/fcimb.2021.679470Frontiers in Cellular and Infection Microbiology, v. 11.2235-2988http://hdl.handle.net/11449/20782510.3389/fcimb.2021.6794702-s2.0-85107224891Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengFrontiers in Cellular and Infection Microbiologyinfo:eu-repo/semantics/openAccess2024-06-21T15:18:19Zoai:repositorio.unesp.br:11449/207825Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:32:47.076372Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
title 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
spellingShingle 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
Bila, Níura Madalena [UNESP]
2-chalcone
biofilms
dermatophytes
mechanism of action
photodynamic therapy
T. mentagrophytes
Trichophyton rubrum
title_short 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
title_full 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
title_fullStr 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
title_full_unstemmed 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
title_sort 2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
author Bila, Níura Madalena [UNESP]
author_facet Bila, Níura Madalena [UNESP]
Costa-Orlandi, Caroline Barcelos [UNESP]
Vaso, Carolina Orlando [UNESP]
Bonatti, Jean Lucas Carvalho [UNESP]
de Assis, Letícia Ribeiro [UNESP]
Regasini, Luís Octavio [UNESP]
Fontana, Carla Raquel [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
author_role author
author2 Costa-Orlandi, Caroline Barcelos [UNESP]
Vaso, Carolina Orlando [UNESP]
Bonatti, Jean Lucas Carvalho [UNESP]
de Assis, Letícia Ribeiro [UNESP]
Regasini, Luís Octavio [UNESP]
Fontana, Carla Raquel [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Maringá (UEM)
dc.contributor.author.fl_str_mv Bila, Níura Madalena [UNESP]
Costa-Orlandi, Caroline Barcelos [UNESP]
Vaso, Carolina Orlando [UNESP]
Bonatti, Jean Lucas Carvalho [UNESP]
de Assis, Letícia Ribeiro [UNESP]
Regasini, Luís Octavio [UNESP]
Fontana, Carla Raquel [UNESP]
Fusco-Almeida, Ana Marisa [UNESP]
Mendes-Giannini, Maria José Soares [UNESP]
dc.subject.por.fl_str_mv 2-chalcone
biofilms
dermatophytes
mechanism of action
photodynamic therapy
T. mentagrophytes
Trichophyton rubrum
topic 2-chalcone
biofilms
dermatophytes
mechanism of action
photodynamic therapy
T. mentagrophytes
Trichophyton rubrum
description Dermatophytes, fungi that cause dermatophytosis, can invade keratinized tissues in humans and animals. The biofilm-forming ability of these fungi was described recently, and it may be correlated with the long treatment period and common recurrences of this mycosis. In this study, we evaluated the anti-dermatophytic and anti-biofilm activity of 2-hydroxychalcone (2-chalcone) in the dark and photodynamic therapy (PDT)-mediated and to determine its mechanism of action. Trichophyton rubrum and Trichophyton mentagrophytes strains were used in the study. The antifungal susceptibility test of planktonic cells, early-stage biofilms, and mature biofilms were performed using colorimetric methods. Topographies were visualized by scanning electron microscopy (SEM). Human skin keratinocyte (HaCat) monolayers were also used in the cytotoxicity assays. The mechanisms of action of 2-chalcone in the dark and under photoexcitation were investigated using confocal microscopy and the quantification of ergosterol, reactive oxygen species (ROS), and death induction by apoptosis/necrosis. All strains, in the planktonic form, were inhibited after treatment with 2-chalcone (minimum inhibitory concentration (MIC) = 7.8-15.6 mg/L), terbinafine (TRB) (MIC = 0.008–0.03 mg/L), and fluconazole (FLZ) (1–512 mg/L). Early-stage biofilm and mature biofilms were inhibited by 2-chalcone at concentrations of 15.6 mg/L and 31.2 mg/L in all tested strains. However, mature biofilms were resistant to all the antifungal drugs tested. When planktonic cells and biofilms (early-stage and mature) were treated with 2-chalcone-mediated PDT, the inhibitory concentrations were reduced by four times (2–7.8 mg/L). SEM images of biofilms treated with 2-chalcone showed cell wall collapse, resulting from a probable extravasation of cytoplasmic content. The toxicity of 2-chalcone in HaCat cells showed higher IC50 values in the dark than under photoexcitation. Further, 2-chalcone targets ergosterol in the cell and promotes the generation of ROS, resulting in cell death by apoptosis and necrosis. Overall, 2-chalcone-mediated PDT is a promising and safe drug candidate against dermatophytes, particularly in anti-biofilm treatment.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:01:38Z
2021-06-25T11:01:38Z
2021-05-13
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3389/fcimb.2021.679470
Frontiers in Cellular and Infection Microbiology, v. 11.
2235-2988
http://hdl.handle.net/11449/207825
10.3389/fcimb.2021.679470
2-s2.0-85107224891
url http://dx.doi.org/10.3389/fcimb.2021.679470
http://hdl.handle.net/11449/207825
identifier_str_mv Frontiers in Cellular and Infection Microbiology, v. 11.
2235-2988
10.3389/fcimb.2021.679470
2-s2.0-85107224891
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Frontiers in Cellular and Infection Microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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