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Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production

Paracoccidioidomycosis (PCM) is a fungal disease caused by organisms of the genus Paracoccidioides spp. The treatment of the disease is lengthy and includes several adverse effects. Various methodologies focus on the search for new treatments against fungal disease, including the repositioning of dr...

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Autores principales: Rocha, Olivia Basso, e Silva, Kleber Santiago Freitas, Moraes, Dayane, Borges, Clayton Luiz, 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/PMC9951877/
https://www.ncbi.nlm.nih.gov/pubmed/36830117
http://dx.doi.org/10.3390/antibiotics12020206
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author Rocha, Olivia Basso
e Silva, Kleber Santiago Freitas
Moraes, Dayane
Borges, Clayton Luiz
Soares, Célia Maria de Almeida
Pereira, Maristela
author_facet Rocha, Olivia Basso
e Silva, Kleber Santiago Freitas
Moraes, Dayane
Borges, Clayton Luiz
Soares, Célia Maria de Almeida
Pereira, Maristela
author_sort Rocha, Olivia Basso
collection PubMed
description Paracoccidioidomycosis (PCM) is a fungal disease caused by organisms of the genus Paracoccidioides spp. The treatment of the disease is lengthy and includes several adverse effects. Various methodologies focus on the search for new treatments against fungal disease, including the repositioning of drugs. Our group showed the fungicidal effect of mebendazole in P. brasiliensis cells. Thus, understanding the effect of exposing fungal cells to mebendazole is significant for further studies in order to demonstrate it as a potential drug for the treatment of PCM. A proteomic analysis of P. brasiliensis exposed to mebendazole was carried out. Analyses showed that exposure strongly affected the pathways related to energy production, such as glycolysis, fermentation, and the electron transport chain. The quantification of adenosine triphosphate (ATP) and mitochondrial activity demonstrated that the drug alters the electron chain, resulting in an increase in oxidative stress. Enzymes such as superoxide dismutase (SOD) and cytochrome c oxidase (Cyt C) were repressed in cells exposed to mebendazole. The concentration of ethanol produced by the cells under treatment demonstrated that the attempt to produce energy through fermentation is also arrested. Thus, the drug inhibits fungal growth through changes in energy metabolism, making it a promising compound for use in the treatment of PCM.
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spelling pubmed-99518772023-02-25 Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production Rocha, Olivia Basso e Silva, Kleber Santiago Freitas Moraes, Dayane Borges, Clayton Luiz Soares, Célia Maria de Almeida Pereira, Maristela Antibiotics (Basel) Article Paracoccidioidomycosis (PCM) is a fungal disease caused by organisms of the genus Paracoccidioides spp. The treatment of the disease is lengthy and includes several adverse effects. Various methodologies focus on the search for new treatments against fungal disease, including the repositioning of drugs. Our group showed the fungicidal effect of mebendazole in P. brasiliensis cells. Thus, understanding the effect of exposing fungal cells to mebendazole is significant for further studies in order to demonstrate it as a potential drug for the treatment of PCM. A proteomic analysis of P. brasiliensis exposed to mebendazole was carried out. Analyses showed that exposure strongly affected the pathways related to energy production, such as glycolysis, fermentation, and the electron transport chain. The quantification of adenosine triphosphate (ATP) and mitochondrial activity demonstrated that the drug alters the electron chain, resulting in an increase in oxidative stress. Enzymes such as superoxide dismutase (SOD) and cytochrome c oxidase (Cyt C) were repressed in cells exposed to mebendazole. The concentration of ethanol produced by the cells under treatment demonstrated that the attempt to produce energy through fermentation is also arrested. Thus, the drug inhibits fungal growth through changes in energy metabolism, making it a promising compound for use in the treatment of PCM. MDPI 2023-01-18 /pmc/articles/PMC9951877/ /pubmed/36830117 http://dx.doi.org/10.3390/antibiotics12020206 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
Rocha, Olivia Basso
e Silva, Kleber Santiago Freitas
Moraes, Dayane
Borges, Clayton Luiz
Soares, Célia Maria de Almeida
Pereira, Maristela
Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title_full Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title_fullStr Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title_full_unstemmed Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title_short Exposure of Paracoccidioides brasiliensis to Mebendazole Leads to Inhibition of Fungal Energy Production
title_sort exposure of paracoccidioides brasiliensis to mebendazole leads to inhibition of fungal energy production
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951877/
https://www.ncbi.nlm.nih.gov/pubmed/36830117
http://dx.doi.org/10.3390/antibiotics12020206
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