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Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil

The study aimed to evaluate the anti-Sporothrix sp. activity of the essential oil of Origanum majorana Linn. (marjoram), its chemical analysis, and its cytotoxic activity. A total of 18 fungal isolates of Sporothrix brasiliensis (n: 17) from humans, dogs and cats, and a standard strain of Sporothrix...

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Autores principales: Waller, Stefanie Bressan, Madrid, Isabel Martins, Ferraz, Vanny, Picoli, Tony, Cleff, Marlete Brum, de Faria, Renata Osório, Meireles, Mário Carlos Araújo, de Mello, João Roberto Braga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052358/
https://www.ncbi.nlm.nih.gov/pubmed/27515466
http://dx.doi.org/10.1016/j.bjm.2016.07.017
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author Waller, Stefanie Bressan
Madrid, Isabel Martins
Ferraz, Vanny
Picoli, Tony
Cleff, Marlete Brum
de Faria, Renata Osório
Meireles, Mário Carlos Araújo
de Mello, João Roberto Braga
author_facet Waller, Stefanie Bressan
Madrid, Isabel Martins
Ferraz, Vanny
Picoli, Tony
Cleff, Marlete Brum
de Faria, Renata Osório
Meireles, Mário Carlos Araújo
de Mello, João Roberto Braga
author_sort Waller, Stefanie Bressan
collection PubMed
description The study aimed to evaluate the anti-Sporothrix sp. activity of the essential oil of Origanum majorana Linn. (marjoram), its chemical analysis, and its cytotoxic activity. A total of 18 fungal isolates of Sporothrix brasiliensis (n: 17) from humans, dogs and cats, and a standard strain of Sporothrix schenckii (n: 1) were tested using the broth microdilution technique (Clinical and Laboratory Standard Institute – CLSI M27-A3) and the results were expressed in minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC). The MIC(50) and MIC(90) of itraconazole against S. brasiliensis were 2 μg/mL and 8 μg/mL, respectively, and the MFC(50) and MFC(90) were 2 μg/mL and >16 μg/mL, respectively, with three S. brasiliensis isolates resistant to antifungal. S. schenckii was sensitive at MIC of 1 μg/mL and MFC of 8 μg/mL. For the oil of O. majorana L., all isolates were susceptible to MIC of ≤2.25–9 mg/mL and MFC of ≤2.25–18 mg/mL. The MIC(50) and MIC(90) were ≤2.25 mg/mL and 4.5 mg/mL, respectively, and the MFC(50/90) values were twice more than the MIC. Twenty-two compounds were identified by gas chromatography with a flame ionization detector (CG-FID) and 1,8-cineole and 4-terpineol were the majority. Through the colorimetric (MTT) assay, the toxicity was observed in 70–80% of VERO cells between 0.078 and 5 mg/mL. For the first time, the study demonstrated the satisfactory in vitro anti-Sporothrix sp. activity of marjoram oil and further studies are needed to ensure its safe and effective use.
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spelling pubmed-50523582016-10-12 Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil Waller, Stefanie Bressan Madrid, Isabel Martins Ferraz, Vanny Picoli, Tony Cleff, Marlete Brum de Faria, Renata Osório Meireles, Mário Carlos Araújo de Mello, João Roberto Braga Braz J Microbiol Veterinary Microbiology The study aimed to evaluate the anti-Sporothrix sp. activity of the essential oil of Origanum majorana Linn. (marjoram), its chemical analysis, and its cytotoxic activity. A total of 18 fungal isolates of Sporothrix brasiliensis (n: 17) from humans, dogs and cats, and a standard strain of Sporothrix schenckii (n: 1) were tested using the broth microdilution technique (Clinical and Laboratory Standard Institute – CLSI M27-A3) and the results were expressed in minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC). The MIC(50) and MIC(90) of itraconazole against S. brasiliensis were 2 μg/mL and 8 μg/mL, respectively, and the MFC(50) and MFC(90) were 2 μg/mL and >16 μg/mL, respectively, with three S. brasiliensis isolates resistant to antifungal. S. schenckii was sensitive at MIC of 1 μg/mL and MFC of 8 μg/mL. For the oil of O. majorana L., all isolates were susceptible to MIC of ≤2.25–9 mg/mL and MFC of ≤2.25–18 mg/mL. The MIC(50) and MIC(90) were ≤2.25 mg/mL and 4.5 mg/mL, respectively, and the MFC(50/90) values were twice more than the MIC. Twenty-two compounds were identified by gas chromatography with a flame ionization detector (CG-FID) and 1,8-cineole and 4-terpineol were the majority. Through the colorimetric (MTT) assay, the toxicity was observed in 70–80% of VERO cells between 0.078 and 5 mg/mL. For the first time, the study demonstrated the satisfactory in vitro anti-Sporothrix sp. activity of marjoram oil and further studies are needed to ensure its safe and effective use. Elsevier 2016-07-29 /pmc/articles/PMC5052358/ /pubmed/27515466 http://dx.doi.org/10.1016/j.bjm.2016.07.017 Text en © 2016 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Veterinary Microbiology
Waller, Stefanie Bressan
Madrid, Isabel Martins
Ferraz, Vanny
Picoli, Tony
Cleff, Marlete Brum
de Faria, Renata Osório
Meireles, Mário Carlos Araújo
de Mello, João Roberto Braga
Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title_full Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title_fullStr Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title_full_unstemmed Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title_short Cytotoxicity and anti-Sporothrix brasiliensis activity of the Origanum majorana Linn. oil
title_sort cytotoxicity and anti-sporothrix brasiliensis activity of the origanum majorana linn. oil
topic Veterinary Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052358/
https://www.ncbi.nlm.nih.gov/pubmed/27515466
http://dx.doi.org/10.1016/j.bjm.2016.07.017
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