Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi

Abstract This study aimed to evaluate the in vitro antifungal activity of terpinen-4-ol, tyrosol, and β-lapachone against strains of Coccidioides posadasii in filamentous phase (n = 22) and Histoplasma capsulatum in both filamentous (n = 40) and yeast phases (n = 13), using the broth dilution methods as described by the Clinical and Laboratory Standards Institute, to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of these compounds. The mechanisms of action of these compounds were also investigated by analyzing their effect on cell membrane permeability and ergosterol synthesis. The MIC and MFCf these compounds against C. posadasii, mycelial H. capsulatum, and yeast-like H. capsulatum, were in the following ranges: 350-5720 µg/mL, 20-2860 µg/mL, and 40-1420 µg/mL, respectively for terpinen-4-ol; 250-4000 µg/mL, 30-2000 µg/mL, and 10-1000 µg/mL, respectively, for tyrosol; and 0.48-7.8 µg/mL, 0.25-16 µg/mL, and 0.125-4 µg/mL, respectively for β-lapachone. These compounds showed a decrease in MIC when the samples were subjected to osmotic stress, suggesting that the compounds acted on the fungal membrane. All the compounds were able to reduce the ergosterol content of the fungal strains. Finally, tyrosol was able to cause a leakage of intracellular molecules.

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Main Authors: Brilhante,Raimunda Sâmia Nogueira, Caetano,Érica Pacheco, Lima,Rita Amanda Chaves de, Marques,Francisca Jakelyne de Farias, Castelo-Branco,Débora de Souza Collares Maia, Melo,Charlline Vládia Silva de, Guedes,Glaucia Morgana de Melo, Oliveira,Jonathas Sales de, Camargo,Zoilo Pires de, Moreira,José Luciano Bezerra, Monteiro,André Jalles, Bandeira,Tereza de Jesus Pinheiro Gomes, Cordeiro,Rossana de Aguiar, Rocha,Marcos Fábio Gadelha, Sidrim,José Júlio Costa
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Microbiologia 2016
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822016000400917
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spelling oai:scielo:S1517-838220160004009172016-11-21Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungiBrilhante,Raimunda Sâmia NogueiraCaetano,Érica PachecoLima,Rita Amanda Chaves deMarques,Francisca Jakelyne de FariasCastelo-Branco,Débora de Souza Collares MaiaMelo,Charlline Vládia Silva deGuedes,Glaucia Morgana de MeloOliveira,Jonathas Sales deCamargo,Zoilo Pires deMoreira,José Luciano BezerraMonteiro,André JallesBandeira,Tereza de Jesus Pinheiro GomesCordeiro,Rossana de AguiarRocha,Marcos Fábio GadelhaSidrim,José Júlio Costa Dimorphic fungi Terpinen-4-ol Tyrosol β-Lapachone Inhibitory effect Abstract This study aimed to evaluate the in vitro antifungal activity of terpinen-4-ol, tyrosol, and β-lapachone against strains of Coccidioides posadasii in filamentous phase (n = 22) and Histoplasma capsulatum in both filamentous (n = 40) and yeast phases (n = 13), using the broth dilution methods as described by the Clinical and Laboratory Standards Institute, to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of these compounds. The mechanisms of action of these compounds were also investigated by analyzing their effect on cell membrane permeability and ergosterol synthesis. The MIC and MFCf these compounds against C. posadasii, mycelial H. capsulatum, and yeast-like H. capsulatum, were in the following ranges: 350-5720 µg/mL, 20-2860 µg/mL, and 40-1420 µg/mL, respectively for terpinen-4-ol; 250-4000 µg/mL, 30-2000 µg/mL, and 10-1000 µg/mL, respectively, for tyrosol; and 0.48-7.8 µg/mL, 0.25-16 µg/mL, and 0.125-4 µg/mL, respectively for β-lapachone. These compounds showed a decrease in MIC when the samples were subjected to osmotic stress, suggesting that the compounds acted on the fungal membrane. All the compounds were able to reduce the ergosterol content of the fungal strains. Finally, tyrosol was able to cause a leakage of intracellular molecules.info:eu-repo/semantics/openAccessSociedade Brasileira de MicrobiologiaBrazilian Journal of Microbiology v.47 n.4 20162016-12-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822016000400917en10.1016/j.bjm.2016.07.015
institution SCIELO
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region America del Sur
libraryname SciELO
language English
format Digital
author Brilhante,Raimunda Sâmia Nogueira
Caetano,Érica Pacheco
Lima,Rita Amanda Chaves de
Marques,Francisca Jakelyne de Farias
Castelo-Branco,Débora de Souza Collares Maia
Melo,Charlline Vládia Silva de
Guedes,Glaucia Morgana de Melo
Oliveira,Jonathas Sales de
Camargo,Zoilo Pires de
Moreira,José Luciano Bezerra
Monteiro,André Jalles
Bandeira,Tereza de Jesus Pinheiro Gomes
Cordeiro,Rossana de Aguiar
Rocha,Marcos Fábio Gadelha
Sidrim,José Júlio Costa
spellingShingle Brilhante,Raimunda Sâmia Nogueira
Caetano,Érica Pacheco
Lima,Rita Amanda Chaves de
Marques,Francisca Jakelyne de Farias
Castelo-Branco,Débora de Souza Collares Maia
Melo,Charlline Vládia Silva de
Guedes,Glaucia Morgana de Melo
Oliveira,Jonathas Sales de
Camargo,Zoilo Pires de
Moreira,José Luciano Bezerra
Monteiro,André Jalles
Bandeira,Tereza de Jesus Pinheiro Gomes
Cordeiro,Rossana de Aguiar
Rocha,Marcos Fábio Gadelha
Sidrim,José Júlio Costa
Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
author_facet Brilhante,Raimunda Sâmia Nogueira
Caetano,Érica Pacheco
Lima,Rita Amanda Chaves de
Marques,Francisca Jakelyne de Farias
Castelo-Branco,Débora de Souza Collares Maia
Melo,Charlline Vládia Silva de
Guedes,Glaucia Morgana de Melo
Oliveira,Jonathas Sales de
Camargo,Zoilo Pires de
Moreira,José Luciano Bezerra
Monteiro,André Jalles
Bandeira,Tereza de Jesus Pinheiro Gomes
Cordeiro,Rossana de Aguiar
Rocha,Marcos Fábio Gadelha
Sidrim,José Júlio Costa
author_sort Brilhante,Raimunda Sâmia Nogueira
title Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
title_short Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
title_full Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
title_fullStr Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
title_full_unstemmed Terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
title_sort terpinen-4-ol, tyrosol, and β-lapachone as potential antifungals against dimorphic fungi
description Abstract This study aimed to evaluate the in vitro antifungal activity of terpinen-4-ol, tyrosol, and β-lapachone against strains of Coccidioides posadasii in filamentous phase (n = 22) and Histoplasma capsulatum in both filamentous (n = 40) and yeast phases (n = 13), using the broth dilution methods as described by the Clinical and Laboratory Standards Institute, to determine the minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of these compounds. The mechanisms of action of these compounds were also investigated by analyzing their effect on cell membrane permeability and ergosterol synthesis. The MIC and MFCf these compounds against C. posadasii, mycelial H. capsulatum, and yeast-like H. capsulatum, were in the following ranges: 350-5720 µg/mL, 20-2860 µg/mL, and 40-1420 µg/mL, respectively for terpinen-4-ol; 250-4000 µg/mL, 30-2000 µg/mL, and 10-1000 µg/mL, respectively, for tyrosol; and 0.48-7.8 µg/mL, 0.25-16 µg/mL, and 0.125-4 µg/mL, respectively for β-lapachone. These compounds showed a decrease in MIC when the samples were subjected to osmotic stress, suggesting that the compounds acted on the fungal membrane. All the compounds were able to reduce the ergosterol content of the fungal strains. Finally, tyrosol was able to cause a leakage of intracellular molecules.
publisher Sociedade Brasileira de Microbiologia
publishDate 2016
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822016000400917
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