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Mesoionic compounds with antifungal activity against Fusarium verticillioides

BACKGROUND: Fungi contaminate the food of humans and animals, are a risk to health, and can cause financial losses. In this work, the antifungal activities of 16 mesoionic compounds (MI 1–16) were evaluated against mycotoxigenic fungi, including Aspergillus spp., Fusarium verticillioides and Penicil...

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Autores principales: Paiva, Rojane de Oliveira, Kneipp, Lucimar Ferreira, dos Reis, Camilla Moretto, Echevarria, Aurea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327949/
https://www.ncbi.nlm.nih.gov/pubmed/25649493
http://dx.doi.org/10.1186/s12866-015-0340-9
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author Paiva, Rojane de Oliveira
Kneipp, Lucimar Ferreira
dos Reis, Camilla Moretto
Echevarria, Aurea
author_facet Paiva, Rojane de Oliveira
Kneipp, Lucimar Ferreira
dos Reis, Camilla Moretto
Echevarria, Aurea
author_sort Paiva, Rojane de Oliveira
collection PubMed
description BACKGROUND: Fungi contaminate the food of humans and animals, are a risk to health, and can cause financial losses. In this work, the antifungal activities of 16 mesoionic compounds (MI 1–16) were evaluated against mycotoxigenic fungi, including Aspergillus spp., Fusarium verticillioides and Penicillium citrinum. Furthermore, the decreased ergosterol in the total lipid content of Fusarium verticillioides was investigated. RESULTS: F. verticillioides was the most sensitive fungus to the mesoionic compounds. Among the evaluated compounds, MI-11 and MI-16 presented higher antifungal effects against F. verticillioides, with MIC values of 7.8 μg/ml, and MI-2 and MI-3 followed, with MICs of 15.6 μg/ml. The most active compounds were those with heterocyclic ring phenyl groups substituted by electron donor moieties (MI-11 and MI-16). Among some compounds with higher activity (MI-2, MI-11 and MI-16), decreased ergosterol content in the total lipid fraction of F. verticillioides was demonstrated. MI-2 reduced the ergosterol content approximately 40% and 80% at concentrations of 7.8 μg/ml and 15.6 μg/ml, respectively, and MI-11 and MI-16 decreased the content by 30% and 50%, respectively, when at a concentration of 7.8 μg/ml. CONCLUSION: These findings indicate that mesoionic compounds have significant antifungal activity against F. verticillioides.
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spelling pubmed-43279492015-02-15 Mesoionic compounds with antifungal activity against Fusarium verticillioides Paiva, Rojane de Oliveira Kneipp, Lucimar Ferreira dos Reis, Camilla Moretto Echevarria, Aurea BMC Microbiol Research Article BACKGROUND: Fungi contaminate the food of humans and animals, are a risk to health, and can cause financial losses. In this work, the antifungal activities of 16 mesoionic compounds (MI 1–16) were evaluated against mycotoxigenic fungi, including Aspergillus spp., Fusarium verticillioides and Penicillium citrinum. Furthermore, the decreased ergosterol in the total lipid content of Fusarium verticillioides was investigated. RESULTS: F. verticillioides was the most sensitive fungus to the mesoionic compounds. Among the evaluated compounds, MI-11 and MI-16 presented higher antifungal effects against F. verticillioides, with MIC values of 7.8 μg/ml, and MI-2 and MI-3 followed, with MICs of 15.6 μg/ml. The most active compounds were those with heterocyclic ring phenyl groups substituted by electron donor moieties (MI-11 and MI-16). Among some compounds with higher activity (MI-2, MI-11 and MI-16), decreased ergosterol content in the total lipid fraction of F. verticillioides was demonstrated. MI-2 reduced the ergosterol content approximately 40% and 80% at concentrations of 7.8 μg/ml and 15.6 μg/ml, respectively, and MI-11 and MI-16 decreased the content by 30% and 50%, respectively, when at a concentration of 7.8 μg/ml. CONCLUSION: These findings indicate that mesoionic compounds have significant antifungal activity against F. verticillioides. BioMed Central 2015-02-04 /pmc/articles/PMC4327949/ /pubmed/25649493 http://dx.doi.org/10.1186/s12866-015-0340-9 Text en © Paiva et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Paiva, Rojane de Oliveira
Kneipp, Lucimar Ferreira
dos Reis, Camilla Moretto
Echevarria, Aurea
Mesoionic compounds with antifungal activity against Fusarium verticillioides
title Mesoionic compounds with antifungal activity against Fusarium verticillioides
title_full Mesoionic compounds with antifungal activity against Fusarium verticillioides
title_fullStr Mesoionic compounds with antifungal activity against Fusarium verticillioides
title_full_unstemmed Mesoionic compounds with antifungal activity against Fusarium verticillioides
title_short Mesoionic compounds with antifungal activity against Fusarium verticillioides
title_sort mesoionic compounds with antifungal activity against fusarium verticillioides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327949/
https://www.ncbi.nlm.nih.gov/pubmed/25649493
http://dx.doi.org/10.1186/s12866-015-0340-9
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