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Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity

Plants belonging to the genus Copaifera are widely used in Brazil due to their antimicrobial properties, among others. The re-emergence of classic fungal diseases as a consequence of antifungal resistance to available drugs has stimulated the search for plant-based compounds with antifungal activity...

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Autores principales: Andrade, Géssica, Orlando, Haniel Chadwick Silva, Scorzoni, Liliana, Pedroso, Reginaldo Santos, Abrão, Fariza, Carvalho, Marco Túlio Menezes, Veneziani, Rodrigo Cassio Sola, Ambrósio, Sérgio Ricardo, Bastos, Jairo Kenupp, Mendes-Giannini, Maria José Soares, Martins, Carlos Henrique Gomes, Pires, Regina Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560146/
https://www.ncbi.nlm.nih.gov/pubmed/32872100
http://dx.doi.org/10.3390/jof6030153
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author Andrade, Géssica
Orlando, Haniel Chadwick Silva
Scorzoni, Liliana
Pedroso, Reginaldo Santos
Abrão, Fariza
Carvalho, Marco Túlio Menezes
Veneziani, Rodrigo Cassio Sola
Ambrósio, Sérgio Ricardo
Bastos, Jairo Kenupp
Mendes-Giannini, Maria José Soares
Martins, Carlos Henrique Gomes
Pires, Regina Helena
author_facet Andrade, Géssica
Orlando, Haniel Chadwick Silva
Scorzoni, Liliana
Pedroso, Reginaldo Santos
Abrão, Fariza
Carvalho, Marco Túlio Menezes
Veneziani, Rodrigo Cassio Sola
Ambrósio, Sérgio Ricardo
Bastos, Jairo Kenupp
Mendes-Giannini, Maria José Soares
Martins, Carlos Henrique Gomes
Pires, Regina Helena
author_sort Andrade, Géssica
collection PubMed
description Plants belonging to the genus Copaifera are widely used in Brazil due to their antimicrobial properties, among others. The re-emergence of classic fungal diseases as a consequence of antifungal resistance to available drugs has stimulated the search for plant-based compounds with antifungal activity, especially against Candida. The Candida-infected Caenorhabditis elegans model was used to evaluate the in vitro antifungal potential of Copaifera leaf extracts and trunk oleoresins against Candida species. The Copaifera leaf extracts exhibited good antifungal activity against all Candida species, with MIC values ranging from 5.86 to 93.75 µg/mL. Both the Copaifera paupera and Copaifera reticulata leaf extracts at 46.87 µg/mL inhibited Candida glabrata biofilm formation and showed no toxicity to C. elegans. The survival of C. glabrata-infected nematodes increased at all the tested extract concentrations. Exposure to Copaifera leaf extracts markedly increased C. glabrata cell vacuolization and cell membrane damage. Therefore, Copaifera leaf extracts are potential candidates for the development of new and safe antifungal agents.
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spelling pubmed-75601462020-10-22 Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity Andrade, Géssica Orlando, Haniel Chadwick Silva Scorzoni, Liliana Pedroso, Reginaldo Santos Abrão, Fariza Carvalho, Marco Túlio Menezes Veneziani, Rodrigo Cassio Sola Ambrósio, Sérgio Ricardo Bastos, Jairo Kenupp Mendes-Giannini, Maria José Soares Martins, Carlos Henrique Gomes Pires, Regina Helena J Fungi (Basel) Article Plants belonging to the genus Copaifera are widely used in Brazil due to their antimicrobial properties, among others. The re-emergence of classic fungal diseases as a consequence of antifungal resistance to available drugs has stimulated the search for plant-based compounds with antifungal activity, especially against Candida. The Candida-infected Caenorhabditis elegans model was used to evaluate the in vitro antifungal potential of Copaifera leaf extracts and trunk oleoresins against Candida species. The Copaifera leaf extracts exhibited good antifungal activity against all Candida species, with MIC values ranging from 5.86 to 93.75 µg/mL. Both the Copaifera paupera and Copaifera reticulata leaf extracts at 46.87 µg/mL inhibited Candida glabrata biofilm formation and showed no toxicity to C. elegans. The survival of C. glabrata-infected nematodes increased at all the tested extract concentrations. Exposure to Copaifera leaf extracts markedly increased C. glabrata cell vacuolization and cell membrane damage. Therefore, Copaifera leaf extracts are potential candidates for the development of new and safe antifungal agents. MDPI 2020-08-28 /pmc/articles/PMC7560146/ /pubmed/32872100 http://dx.doi.org/10.3390/jof6030153 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Andrade, Géssica
Orlando, Haniel Chadwick Silva
Scorzoni, Liliana
Pedroso, Reginaldo Santos
Abrão, Fariza
Carvalho, Marco Túlio Menezes
Veneziani, Rodrigo Cassio Sola
Ambrósio, Sérgio Ricardo
Bastos, Jairo Kenupp
Mendes-Giannini, Maria José Soares
Martins, Carlos Henrique Gomes
Pires, Regina Helena
Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title_full Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title_fullStr Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title_full_unstemmed Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title_short Brazilian Copaifera Species: Antifungal Activity against Clinically Relevant Candida Species, Cellular Target, and In Vivo Toxicity
title_sort brazilian copaifera species: antifungal activity against clinically relevant candida species, cellular target, and in vivo toxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560146/
https://www.ncbi.nlm.nih.gov/pubmed/32872100
http://dx.doi.org/10.3390/jof6030153
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