2-Hydroxychalcone as a Potent Compound and Photosensitizer Against Dermatophyte Biofilms
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , |
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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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 |
|
_version_ |
1808128376134696960 |