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Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air

In this paper, we demonstrate the ability of Arabidopsis thaliana to detect different mixtures of volatile organic compounds (VOCs) emitted by the common indoor fungus, Aspergillus versicolor, and demonstrate the potential usage of the plant as a bioindicator to monitor fungal VOCs in indoor air. We...

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Autores principales: Lee, Samantha, Hung, Richard, Yin, Guohua, Klich, Maren A., Grimm, Casey, Bennett, Joan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Mycology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078129/
https://www.ncbi.nlm.nih.gov/pubmed/27790067
http://dx.doi.org/10.5941/MYCO.2016.44.3.162
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author Lee, Samantha
Hung, Richard
Yin, Guohua
Klich, Maren A.
Grimm, Casey
Bennett, Joan W.
author_facet Lee, Samantha
Hung, Richard
Yin, Guohua
Klich, Maren A.
Grimm, Casey
Bennett, Joan W.
author_sort Lee, Samantha
collection PubMed
description In this paper, we demonstrate the ability of Arabidopsis thaliana to detect different mixtures of volatile organic compounds (VOCs) emitted by the common indoor fungus, Aspergillus versicolor, and demonstrate the potential usage of the plant as a bioindicator to monitor fungal VOCs in indoor air. We evaluated the volatile production of Aspergillus versicolor strains SRRC 108 (NRRL 3449) and SRRC 2559 (ATCC 32662) grown on nutrient rich fungal medium, and grown under conditions to mimic the substrate encountered in the built environment where fungi would typically grow indoors (moist wallboard and ceiling tiles). Using headspace solid phase microextraction/gas chromatography-mass spectrometry, we analyzed VOC profiles of the two strains. The most abundant compound produced by both strains on all three media was 1-octen-3-ol. Strain SRRC 2559 made several terpenes not detected from strain SRRC 108. Using a split-plate bioassay, we grew Arabidopsis thaliana in a shared atmosphere with VOCs from the two strains of Aspergillus versicolor grown on yeast extract sucrose medium. The VOCs emitted by SRRC 2559 had an adverse impact on seed germination and plant growth. Chemical standards of individual VOCs from the Aspergillus versicolor mixture (2-methyl-1-butanol, 3-methyl-1-butanol, 1-octen-3-ol, limonene, and β-farnesene), and β-caryophyllene were tested one by one in seed germination and vegetative plant growth assays. The most inhibitory compound to both seed germination and plant growth was 1-octen-3-ol. Our data suggest that Arabidopsis is a useful model for monitoring indoor air quality as it is sensitive to naturally emitted fungal volatile mixtures as well as to chemical standards of individual compounds, and it exhibits relatively quick concentration- and duration-dependent responses.
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spelling pubmed-50781292016-10-27 Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air Lee, Samantha Hung, Richard Yin, Guohua Klich, Maren A. Grimm, Casey Bennett, Joan W. Mycobiology Research Article In this paper, we demonstrate the ability of Arabidopsis thaliana to detect different mixtures of volatile organic compounds (VOCs) emitted by the common indoor fungus, Aspergillus versicolor, and demonstrate the potential usage of the plant as a bioindicator to monitor fungal VOCs in indoor air. We evaluated the volatile production of Aspergillus versicolor strains SRRC 108 (NRRL 3449) and SRRC 2559 (ATCC 32662) grown on nutrient rich fungal medium, and grown under conditions to mimic the substrate encountered in the built environment where fungi would typically grow indoors (moist wallboard and ceiling tiles). Using headspace solid phase microextraction/gas chromatography-mass spectrometry, we analyzed VOC profiles of the two strains. The most abundant compound produced by both strains on all three media was 1-octen-3-ol. Strain SRRC 2559 made several terpenes not detected from strain SRRC 108. Using a split-plate bioassay, we grew Arabidopsis thaliana in a shared atmosphere with VOCs from the two strains of Aspergillus versicolor grown on yeast extract sucrose medium. The VOCs emitted by SRRC 2559 had an adverse impact on seed germination and plant growth. Chemical standards of individual VOCs from the Aspergillus versicolor mixture (2-methyl-1-butanol, 3-methyl-1-butanol, 1-octen-3-ol, limonene, and β-farnesene), and β-caryophyllene were tested one by one in seed germination and vegetative plant growth assays. The most inhibitory compound to both seed germination and plant growth was 1-octen-3-ol. Our data suggest that Arabidopsis is a useful model for monitoring indoor air quality as it is sensitive to naturally emitted fungal volatile mixtures as well as to chemical standards of individual compounds, and it exhibits relatively quick concentration- and duration-dependent responses. The Korean Society of Mycology 2016-09 2016-09-30 /pmc/articles/PMC5078129/ /pubmed/27790067 http://dx.doi.org/10.5941/MYCO.2016.44.3.162 Text en © The Korean Society of Mycology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lee, Samantha
Hung, Richard
Yin, Guohua
Klich, Maren A.
Grimm, Casey
Bennett, Joan W.
Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title_full Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title_fullStr Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title_full_unstemmed Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title_short Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air
title_sort arabidopsis thaliana as bioindicator of fungal vocs in indoor air
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078129/
https://www.ncbi.nlm.nih.gov/pubmed/27790067
http://dx.doi.org/10.5941/MYCO.2016.44.3.162
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