Cargando…

Microbiome interplay: plants alter microbial abundance and diversity within the built environment

The built indoor microbiome has importance for human health. Residents leave their microbial fingerprint but nothing is known about the transfer from plants. Our hypothesis that indoor plants contribute substantially to the microbial abundance and diversity in the built environment was experimentall...

Descripción completa

Detalles Bibliográficos
Autores principales: Mahnert, Alexander, Moissl-Eichinger, Christine, Berg, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552223/
https://www.ncbi.nlm.nih.gov/pubmed/26379656
http://dx.doi.org/10.3389/fmicb.2015.00887
_version_ 1782387699248791552
author Mahnert, Alexander
Moissl-Eichinger, Christine
Berg, Gabriele
author_facet Mahnert, Alexander
Moissl-Eichinger, Christine
Berg, Gabriele
author_sort Mahnert, Alexander
collection PubMed
description The built indoor microbiome has importance for human health. Residents leave their microbial fingerprint but nothing is known about the transfer from plants. Our hypothesis that indoor plants contribute substantially to the microbial abundance and diversity in the built environment was experimentally confirmed as proof of principle by analyzing the microbiome of the spider plant Chlorophytum comosum in relation to their surroundings. The abundance of Archaea, Bacteria, and Eukaryota (fungi) increased on surrounding floor and wall surfaces within 6 months of plant isolation in a cleaned indoor environment, whereas the microbial abundance on plant leaves and indoor air remained stable. We observed a microbiome shift: the bacterial diversity on surfaces increased significantly but fungal diversity decreased. The majority of cells were intact at the time of samplings and thus most probably alive including diverse Archaea as yet unknown phyllosphere inhabitants. LEfSe and network analysis showed that most microbes were dispersed from plant leaves to the surrounding surfaces. This led to an increase of specific taxa including spore-forming fungi with potential allergic potential but also beneficial plant-associated bacteria, e.g., Paenibacillus. This study demonstrates for the first time that plants can alter the microbiome of a built environment, which supports the significance of plants and provides insights into the complex interplay of plants, microbiomes and human beings.
format Online
Article
Text
id pubmed-4552223
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-45522232015-09-14 Microbiome interplay: plants alter microbial abundance and diversity within the built environment Mahnert, Alexander Moissl-Eichinger, Christine Berg, Gabriele Front Microbiol Microbiology The built indoor microbiome has importance for human health. Residents leave their microbial fingerprint but nothing is known about the transfer from plants. Our hypothesis that indoor plants contribute substantially to the microbial abundance and diversity in the built environment was experimentally confirmed as proof of principle by analyzing the microbiome of the spider plant Chlorophytum comosum in relation to their surroundings. The abundance of Archaea, Bacteria, and Eukaryota (fungi) increased on surrounding floor and wall surfaces within 6 months of plant isolation in a cleaned indoor environment, whereas the microbial abundance on plant leaves and indoor air remained stable. We observed a microbiome shift: the bacterial diversity on surfaces increased significantly but fungal diversity decreased. The majority of cells were intact at the time of samplings and thus most probably alive including diverse Archaea as yet unknown phyllosphere inhabitants. LEfSe and network analysis showed that most microbes were dispersed from plant leaves to the surrounding surfaces. This led to an increase of specific taxa including spore-forming fungi with potential allergic potential but also beneficial plant-associated bacteria, e.g., Paenibacillus. This study demonstrates for the first time that plants can alter the microbiome of a built environment, which supports the significance of plants and provides insights into the complex interplay of plants, microbiomes and human beings. Frontiers Media S.A. 2015-08-28 /pmc/articles/PMC4552223/ /pubmed/26379656 http://dx.doi.org/10.3389/fmicb.2015.00887 Text en Copyright © 2015 Mahnert, Moissl-Eichinger and Berg. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Mahnert, Alexander
Moissl-Eichinger, Christine
Berg, Gabriele
Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title_full Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title_fullStr Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title_full_unstemmed Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title_short Microbiome interplay: plants alter microbial abundance and diversity within the built environment
title_sort microbiome interplay: plants alter microbial abundance and diversity within the built environment
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552223/
https://www.ncbi.nlm.nih.gov/pubmed/26379656
http://dx.doi.org/10.3389/fmicb.2015.00887
work_keys_str_mv AT mahnertalexander microbiomeinterplayplantsaltermicrobialabundanceanddiversitywithinthebuiltenvironment
AT moissleichingerchristine microbiomeinterplayplantsaltermicrobialabundanceanddiversitywithinthebuiltenvironment
AT berggabriele microbiomeinterplayplantsaltermicrobialabundanceanddiversitywithinthebuiltenvironment