Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.

Genotyping studies of Australian Scedosporium isolates have revealed the strong prevalence of a recently described species: Scedosporium aurantiacum. In addition to occurring in the environment, this fungus is also known to colonise the respiratory tracts of cystic fibrosis (CF) patients. A high thr...

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Main Authors: Jashanpreet Kaur, Shu Yao Duan, Lea A I Vaas, Anahit Penesyan, Wieland Meyer, Ian T Paulsen, Helena Nevalainen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4374879?pdf=render
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spelling doaj-a745df3eaf8846f9a8b82939f078039c2020-11-25T01:18:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012235410.1371/journal.pone.0122354Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.Jashanpreet KaurShu Yao DuanLea A I VaasAnahit PenesyanWieland MeyerIan T PaulsenHelena NevalainenGenotyping studies of Australian Scedosporium isolates have revealed the strong prevalence of a recently described species: Scedosporium aurantiacum. In addition to occurring in the environment, this fungus is also known to colonise the respiratory tracts of cystic fibrosis (CF) patients. A high throughput Phenotype Microarray (PM) analysis using 94 assorted substrates (sugars, amino acids, hexose-acids and carboxylic acids) was carried out for four isolates exhibiting different levels of virulence, determined using a Galleria mellonella infection model. A significant difference was observed in the substrate utilisation patterns of strains displaying differential virulence. For example, certain sugars such as sucrose (saccharose) were utilised only by low virulence strains whereas some sugar derivatives such as D-turanose promoted respiration only in the more virulent strains. Strains with a higher level of virulence also displayed flexibility and metabolic adaptability at two different temperature conditions tested (28 and 37°C). Phenotype microarray data were integrated with the whole-genome sequence data of S. aurantiacum to reconstruct a pathway map for the metabolism of selected substrates to further elucidate differences between the strains.http://europepmc.org/articles/PMC4374879?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jashanpreet Kaur
Shu Yao Duan
Lea A I Vaas
Anahit Penesyan
Wieland Meyer
Ian T Paulsen
Helena Nevalainen
spellingShingle Jashanpreet Kaur
Shu Yao Duan
Lea A I Vaas
Anahit Penesyan
Wieland Meyer
Ian T Paulsen
Helena Nevalainen
Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
PLoS ONE
author_facet Jashanpreet Kaur
Shu Yao Duan
Lea A I Vaas
Anahit Penesyan
Wieland Meyer
Ian T Paulsen
Helena Nevalainen
author_sort Jashanpreet Kaur
title Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
title_short Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
title_full Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
title_fullStr Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
title_full_unstemmed Phenotypic profiling of Scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
title_sort phenotypic profiling of scedosporium aurantiacum, an opportunistic pathogen colonizing human lungs.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Genotyping studies of Australian Scedosporium isolates have revealed the strong prevalence of a recently described species: Scedosporium aurantiacum. In addition to occurring in the environment, this fungus is also known to colonise the respiratory tracts of cystic fibrosis (CF) patients. A high throughput Phenotype Microarray (PM) analysis using 94 assorted substrates (sugars, amino acids, hexose-acids and carboxylic acids) was carried out for four isolates exhibiting different levels of virulence, determined using a Galleria mellonella infection model. A significant difference was observed in the substrate utilisation patterns of strains displaying differential virulence. For example, certain sugars such as sucrose (saccharose) were utilised only by low virulence strains whereas some sugar derivatives such as D-turanose promoted respiration only in the more virulent strains. Strains with a higher level of virulence also displayed flexibility and metabolic adaptability at two different temperature conditions tested (28 and 37°C). Phenotype microarray data were integrated with the whole-genome sequence data of S. aurantiacum to reconstruct a pathway map for the metabolism of selected substrates to further elucidate differences between the strains.
url http://europepmc.org/articles/PMC4374879?pdf=render
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