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Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways

Background: The treatment of paracoccidioidomycosis (PCM) is a challenge, and the discovery of new antifungal compounds is crucial. The phenacylideneoxindoles exhibited promising antifungal activity against Paracoccidioides spp., but their mode of action remains unknown. Methods: Through proteomic a...

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Autores principales: Silva, Lívia do Carmo, Rocha, Olivia Basso, Portis, Igor Godinho, Santos, Thaynara Gonzaga, Freitas e Silva, Kleber Santiago, dos Santos Filho, Raimundo Francisco, Cunha, Silvio, Alonso, Antônio, Soares, Célia Maria de Almeida, Pereira, Maristela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455990/
https://www.ncbi.nlm.nih.gov/pubmed/37623625
http://dx.doi.org/10.3390/jof9080854
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author Silva, Lívia do Carmo
Rocha, Olivia Basso
Portis, Igor Godinho
Santos, Thaynara Gonzaga
Freitas e Silva, Kleber Santiago
dos Santos Filho, Raimundo Francisco
Cunha, Silvio
Alonso, Antônio
Soares, Célia Maria de Almeida
Pereira, Maristela
author_facet Silva, Lívia do Carmo
Rocha, Olivia Basso
Portis, Igor Godinho
Santos, Thaynara Gonzaga
Freitas e Silva, Kleber Santiago
dos Santos Filho, Raimundo Francisco
Cunha, Silvio
Alonso, Antônio
Soares, Célia Maria de Almeida
Pereira, Maristela
author_sort Silva, Lívia do Carmo
collection PubMed
description Background: The treatment of paracoccidioidomycosis (PCM) is a challenge, and the discovery of new antifungal compounds is crucial. The phenacylideneoxindoles exhibited promising antifungal activity against Paracoccidioides spp., but their mode of action remains unknown. Methods: Through proteomic analysis, we investigated the effects of (E)-3-(2-oxo-2-phenylethylidene)indolin-2-one on P. brasiliensis. In addition, we investigated the metabolic alterations of P. brasiliensis in response to the compound. Furthermore, the effects of the compound on the membrane, ethanol production, and reactive oxygen species (ROS) production were verified. Results: We identified differentially regulated proteins that revealed significant metabolic reorganization, including an increase in ethanol production, suggesting the activation of alcoholic fermentation and alterations in the rigidity of fungal cell membrane with an increase of the ergosterol content and formation of ROS. Conclusions: These findings enhance our understanding of the mode of action and response of P. brasiliensis to the investigated promising antifungal compound, emphasizing its potential as a candidate for the treatment of PCM.
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spelling pubmed-104559902023-08-26 Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways Silva, Lívia do Carmo Rocha, Olivia Basso Portis, Igor Godinho Santos, Thaynara Gonzaga Freitas e Silva, Kleber Santiago dos Santos Filho, Raimundo Francisco Cunha, Silvio Alonso, Antônio Soares, Célia Maria de Almeida Pereira, Maristela J Fungi (Basel) Article Background: The treatment of paracoccidioidomycosis (PCM) is a challenge, and the discovery of new antifungal compounds is crucial. The phenacylideneoxindoles exhibited promising antifungal activity against Paracoccidioides spp., but their mode of action remains unknown. Methods: Through proteomic analysis, we investigated the effects of (E)-3-(2-oxo-2-phenylethylidene)indolin-2-one on P. brasiliensis. In addition, we investigated the metabolic alterations of P. brasiliensis in response to the compound. Furthermore, the effects of the compound on the membrane, ethanol production, and reactive oxygen species (ROS) production were verified. Results: We identified differentially regulated proteins that revealed significant metabolic reorganization, including an increase in ethanol production, suggesting the activation of alcoholic fermentation and alterations in the rigidity of fungal cell membrane with an increase of the ergosterol content and formation of ROS. Conclusions: These findings enhance our understanding of the mode of action and response of P. brasiliensis to the investigated promising antifungal compound, emphasizing its potential as a candidate for the treatment of PCM. MDPI 2023-08-16 /pmc/articles/PMC10455990/ /pubmed/37623625 http://dx.doi.org/10.3390/jof9080854 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Silva, Lívia do Carmo
Rocha, Olivia Basso
Portis, Igor Godinho
Santos, Thaynara Gonzaga
Freitas e Silva, Kleber Santiago
dos Santos Filho, Raimundo Francisco
Cunha, Silvio
Alonso, Antônio
Soares, Célia Maria de Almeida
Pereira, Maristela
Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title_full Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title_fullStr Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title_full_unstemmed Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title_short Proteomic Profiling of Paracoccidioides brasiliensis in Response to Phenacylideneoxindol Derivative: Unveiling Molecular Targets and Pathways
title_sort proteomic profiling of paracoccidioides brasiliensis in response to phenacylideneoxindol derivative: unveiling molecular targets and pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455990/
https://www.ncbi.nlm.nih.gov/pubmed/37623625
http://dx.doi.org/10.3390/jof9080854
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