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Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum

Scedosporium aurantiacum is an opportunistic filamentous fungus increasingly isolated from the sputum of cystic fibrosis patients, and is especially prevalent in Australia. At the moment, very little is known about the infection mechanism of this fungus. Secreted proteases have been shown to contrib...

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Autores principales: Han, Zhiping, Kautto, Liisa, Nevalainen, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218550/
https://www.ncbi.nlm.nih.gov/pubmed/28060882
http://dx.doi.org/10.1371/journal.pone.0169403
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author Han, Zhiping
Kautto, Liisa
Nevalainen, Helena
author_facet Han, Zhiping
Kautto, Liisa
Nevalainen, Helena
author_sort Han, Zhiping
collection PubMed
description Scedosporium aurantiacum is an opportunistic filamentous fungus increasingly isolated from the sputum of cystic fibrosis patients, and is especially prevalent in Australia. At the moment, very little is known about the infection mechanism of this fungus. Secreted proteases have been shown to contribute to fungal virulence in several studies with other fungi. Here we have compared the profiles of proteases secreted by a clinical isolate Scedosporium aurantiacum (WM 06.482) and an environmental strain (WM 10.136) grown on a synthetic cystic fibrosis sputum medium supplemented with casein or mucin. Protease activity was assessed using class-specific substrates and inhibitors. Subtilisin-like and trypsin-like serine protease activity was detected in all cultures. The greatest difference in the secretion of proteases between the two strains occurred in mucin-supplemented medium, where the activities of the elastase-like, trypsin-like and aspartic proteases were, overall, 2.5–75 fold higher in the clinical strain compared to the environmental strain. Proteases secreted by the two strains in the mucin-supplemented medium were further analyzed by mass spectrometry. Six homologs of fungal proteases were identified from the clinical strain and five from the environmental strain. Of these, three were common for both strains including a subtilisin peptidase, a putative leucine aminopeptidase and a PA-SaNapH-like protease. Trypsin-like protease was identified by mass spectrometry only in the clinical isolate even though trypsin-like activity was present in all cultures. In contrast, high elastase-like activity was measured in the culture supernatant of the clinical strain but could not be identified by mass spectrometry searching against other fungi in the NCBI database. Future availability of an annotated genome will help finalise identification of the S. aurantiacum proteases.
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spelling pubmed-52185502017-01-19 Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum Han, Zhiping Kautto, Liisa Nevalainen, Helena PLoS One Research Article Scedosporium aurantiacum is an opportunistic filamentous fungus increasingly isolated from the sputum of cystic fibrosis patients, and is especially prevalent in Australia. At the moment, very little is known about the infection mechanism of this fungus. Secreted proteases have been shown to contribute to fungal virulence in several studies with other fungi. Here we have compared the profiles of proteases secreted by a clinical isolate Scedosporium aurantiacum (WM 06.482) and an environmental strain (WM 10.136) grown on a synthetic cystic fibrosis sputum medium supplemented with casein or mucin. Protease activity was assessed using class-specific substrates and inhibitors. Subtilisin-like and trypsin-like serine protease activity was detected in all cultures. The greatest difference in the secretion of proteases between the two strains occurred in mucin-supplemented medium, where the activities of the elastase-like, trypsin-like and aspartic proteases were, overall, 2.5–75 fold higher in the clinical strain compared to the environmental strain. Proteases secreted by the two strains in the mucin-supplemented medium were further analyzed by mass spectrometry. Six homologs of fungal proteases were identified from the clinical strain and five from the environmental strain. Of these, three were common for both strains including a subtilisin peptidase, a putative leucine aminopeptidase and a PA-SaNapH-like protease. Trypsin-like protease was identified by mass spectrometry only in the clinical isolate even though trypsin-like activity was present in all cultures. In contrast, high elastase-like activity was measured in the culture supernatant of the clinical strain but could not be identified by mass spectrometry searching against other fungi in the NCBI database. Future availability of an annotated genome will help finalise identification of the S. aurantiacum proteases. Public Library of Science 2017-01-06 /pmc/articles/PMC5218550/ /pubmed/28060882 http://dx.doi.org/10.1371/journal.pone.0169403 Text en © 2017 Han 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Han, Zhiping
Kautto, Liisa
Nevalainen, Helena
Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title_full Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title_fullStr Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title_full_unstemmed Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title_short Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum
title_sort secretion of proteases by an opportunistic fungal pathogen scedosporium aurantiacum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5218550/
https://www.ncbi.nlm.nih.gov/pubmed/28060882
http://dx.doi.org/10.1371/journal.pone.0169403
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