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Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells
Inhalation of Aspergillus fumigatus conidia can cause severe aspergillosis in immunosuppressed people. A. fumigatus produces a large number of secondary metabolites, some of which are airborne by conidia and whose toxicity to the respiratory tract has not been investigated. We found that spores of A...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272003/ https://www.ncbi.nlm.nih.gov/pubmed/22319557 http://dx.doi.org/10.1371/journal.pone.0029906 |
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author | Gauthier, Thierry Wang, Xiaodi Sifuentes Dos Santos, Joice Fysikopoulos, Athanasios Tadrist, Souria Canlet, Cécile Artigot, Marie Pierre Loiseau, Nicolas Oswald, Isabelle P. Puel, Olivier |
author_facet | Gauthier, Thierry Wang, Xiaodi Sifuentes Dos Santos, Joice Fysikopoulos, Athanasios Tadrist, Souria Canlet, Cécile Artigot, Marie Pierre Loiseau, Nicolas Oswald, Isabelle P. Puel, Olivier |
author_sort | Gauthier, Thierry |
collection | PubMed |
description | Inhalation of Aspergillus fumigatus conidia can cause severe aspergillosis in immunosuppressed people. A. fumigatus produces a large number of secondary metabolites, some of which are airborne by conidia and whose toxicity to the respiratory tract has not been investigated. We found that spores of A. fumigatus contain five main compounds, tryptoquivaline F, fumiquinazoline C, questin, monomethylsulochrin and trypacidin. Fractionation of culture extracts using RP-HPLC and LC-MS showed that samples containing questin, monomethylsulochrin and trypacidin were toxic to the human A549 lung cell line. These compounds were purified and their structure verified using NMR in order to compare their toxicity against A549 cells. Trypacidin was the most toxic, decreasing cell viability and triggering cell lysis, both effects occurring at an IC(50) close to 7 µM. Trypacidin toxicity was also observed in the same concentration range on human bronchial epithelial cells. In the first hour of exposure, trypacidin initiates the intracellular formation of nitric oxide (NO) and hydrogen peroxide (H(2)O(2)). This oxidative stress triggers necrotic cell death in the following 24 h. The apoptosis pathway, moreover, was not involved in the cell death process as trypacidin did not induce apoptotic bodies or a decrease in mitochondrial membrane potential. This is the first time that the toxicity of trypacidin to lung cells has been reported. |
format | Online Article Text |
id | pubmed-3272003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32720032012-02-08 Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells Gauthier, Thierry Wang, Xiaodi Sifuentes Dos Santos, Joice Fysikopoulos, Athanasios Tadrist, Souria Canlet, Cécile Artigot, Marie Pierre Loiseau, Nicolas Oswald, Isabelle P. Puel, Olivier PLoS One Research Article Inhalation of Aspergillus fumigatus conidia can cause severe aspergillosis in immunosuppressed people. A. fumigatus produces a large number of secondary metabolites, some of which are airborne by conidia and whose toxicity to the respiratory tract has not been investigated. We found that spores of A. fumigatus contain five main compounds, tryptoquivaline F, fumiquinazoline C, questin, monomethylsulochrin and trypacidin. Fractionation of culture extracts using RP-HPLC and LC-MS showed that samples containing questin, monomethylsulochrin and trypacidin were toxic to the human A549 lung cell line. These compounds were purified and their structure verified using NMR in order to compare their toxicity against A549 cells. Trypacidin was the most toxic, decreasing cell viability and triggering cell lysis, both effects occurring at an IC(50) close to 7 µM. Trypacidin toxicity was also observed in the same concentration range on human bronchial epithelial cells. In the first hour of exposure, trypacidin initiates the intracellular formation of nitric oxide (NO) and hydrogen peroxide (H(2)O(2)). This oxidative stress triggers necrotic cell death in the following 24 h. The apoptosis pathway, moreover, was not involved in the cell death process as trypacidin did not induce apoptotic bodies or a decrease in mitochondrial membrane potential. This is the first time that the toxicity of trypacidin to lung cells has been reported. Public Library of Science 2012-02-03 /pmc/articles/PMC3272003/ /pubmed/22319557 http://dx.doi.org/10.1371/journal.pone.0029906 Text en Gauthier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gauthier, Thierry Wang, Xiaodi Sifuentes Dos Santos, Joice Fysikopoulos, Athanasios Tadrist, Souria Canlet, Cécile Artigot, Marie Pierre Loiseau, Nicolas Oswald, Isabelle P. Puel, Olivier Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title | Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title_full | Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title_fullStr | Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title_full_unstemmed | Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title_short | Trypacidin, a Spore-Borne Toxin from Aspergillus fumigatus, Is Cytotoxic to Lung Cells |
title_sort | trypacidin, a spore-borne toxin from aspergillus fumigatus, is cytotoxic to lung cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272003/ https://www.ncbi.nlm.nih.gov/pubmed/22319557 http://dx.doi.org/10.1371/journal.pone.0029906 |
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