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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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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. |
format | Online Article Text |
id | pubmed-4327949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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