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Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity

Exposure to biodiverse aerobiomes supports human health, but it is unclear which ecological factors influence exposure. Few studies have investigated near-surface green space aerobiome dynamics, and no studies have reported aerobiome vertical stratification in different urban green spaces. We used c...

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Autores principales: Robinson, Jake M., Cando-Dumancela, Christian, Antwis, Rachael E., Cameron, Ross, Liddicoat, Craig, Poudel, Ravin, Weinstein, Philip, Breed, Martin F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096821/
https://www.ncbi.nlm.nih.gov/pubmed/33947905
http://dx.doi.org/10.1038/s41598-021-89065-y
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author Robinson, Jake M.
Cando-Dumancela, Christian
Antwis, Rachael E.
Cameron, Ross
Liddicoat, Craig
Poudel, Ravin
Weinstein, Philip
Breed, Martin F.
author_facet Robinson, Jake M.
Cando-Dumancela, Christian
Antwis, Rachael E.
Cameron, Ross
Liddicoat, Craig
Poudel, Ravin
Weinstein, Philip
Breed, Martin F.
author_sort Robinson, Jake M.
collection PubMed
description Exposure to biodiverse aerobiomes supports human health, but it is unclear which ecological factors influence exposure. Few studies have investigated near-surface green space aerobiome dynamics, and no studies have reported aerobiome vertical stratification in different urban green spaces. We used columnar sampling and next generation sequencing of the bacterial 16S rRNA gene, combined with geospatial and network analyses to investigate urban green space aerobiome spatio-compositional dynamics. We show a strong effect of habitat on bacterial diversity and network complexity. We observed aerobiome vertical stratification and network complexity that was contingent on habitat type. Tree density, closer proximity, and canopy coverage associated with greater aerobiome alpha diversity. Grassland aerobiomes exhibited greater proportions of putative pathogens compared to scrub, and also stratified vertically. We provide novel insights into the urban ecosystem with potential importance for public health, whereby the possibility of differential aerobiome exposures appears to depend on habitat type and height in the airspace. This has important implications for managing urban landscapes for the regulation of aerobiome exposure.
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spelling pubmed-80968212021-05-05 Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity Robinson, Jake M. Cando-Dumancela, Christian Antwis, Rachael E. Cameron, Ross Liddicoat, Craig Poudel, Ravin Weinstein, Philip Breed, Martin F. Sci Rep Article Exposure to biodiverse aerobiomes supports human health, but it is unclear which ecological factors influence exposure. Few studies have investigated near-surface green space aerobiome dynamics, and no studies have reported aerobiome vertical stratification in different urban green spaces. We used columnar sampling and next generation sequencing of the bacterial 16S rRNA gene, combined with geospatial and network analyses to investigate urban green space aerobiome spatio-compositional dynamics. We show a strong effect of habitat on bacterial diversity and network complexity. We observed aerobiome vertical stratification and network complexity that was contingent on habitat type. Tree density, closer proximity, and canopy coverage associated with greater aerobiome alpha diversity. Grassland aerobiomes exhibited greater proportions of putative pathogens compared to scrub, and also stratified vertically. We provide novel insights into the urban ecosystem with potential importance for public health, whereby the possibility of differential aerobiome exposures appears to depend on habitat type and height in the airspace. This has important implications for managing urban landscapes for the regulation of aerobiome exposure. Nature Publishing Group UK 2021-05-04 /pmc/articles/PMC8096821/ /pubmed/33947905 http://dx.doi.org/10.1038/s41598-021-89065-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Robinson, Jake M.
Cando-Dumancela, Christian
Antwis, Rachael E.
Cameron, Ross
Liddicoat, Craig
Poudel, Ravin
Weinstein, Philip
Breed, Martin F.
Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title_full Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title_fullStr Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title_full_unstemmed Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title_short Exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
title_sort exposure to airborne bacteria depends upon vertical stratification and vegetation complexity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096821/
https://www.ncbi.nlm.nih.gov/pubmed/33947905
http://dx.doi.org/10.1038/s41598-021-89065-y
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