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Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning
The microbiota of the built environment is linked to usage, materials and, perhaps most importantly, human health. Many studies have attempted to identify ways of modulating microbial communities within built environments to promote health. None have explored how these complex communities assemble i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516947/ https://www.ncbi.nlm.nih.gov/pubmed/37740013 http://dx.doi.org/10.1038/s41598-023-42427-0 |
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author | Young, Gregory R. Sherry, Angela Smith, Darren L. |
author_facet | Young, Gregory R. Sherry, Angela Smith, Darren L. |
author_sort | Young, Gregory R. |
collection | PubMed |
description | The microbiota of the built environment is linked to usage, materials and, perhaps most importantly, human health. Many studies have attempted to identify ways of modulating microbial communities within built environments to promote health. None have explored how these complex communities assemble initially, following construction of new built environments. This study used high-throughput targeted sequencing approaches to explore bacterial community acquisition and development throughout the construction of a new build. Microbial sampling spanned from site identification, through the construction process to commissioning and use. Following commissioning of the building, bacterial richness and diversity were significantly reduced (P < 0.001) and community structure was altered (R(2) = 0.14; P = 0.001). Greater longitudinal community stability was observed in outdoor environments than indoor environments. Community flux in indoor environments was associated with human interventions driving environmental selection, which increased 10.4% in indoor environments following commissioning. Increased environmental selection coincided with a 12% reduction in outdoor community influence on indoor microbiomes (P = 2.00 × 10(–15)). Indoor communities became significantly enriched with human associated genera including Escherichia, Pseudomonas, and Klebsiella spp. These data represent the first to characterize the initial assembly of bacterial communities in built environments and will inform future studies aiming to modulate built environment microbiota. |
format | Online Article Text |
id | pubmed-10516947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105169472023-09-24 Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning Young, Gregory R. Sherry, Angela Smith, Darren L. Sci Rep Article The microbiota of the built environment is linked to usage, materials and, perhaps most importantly, human health. Many studies have attempted to identify ways of modulating microbial communities within built environments to promote health. None have explored how these complex communities assemble initially, following construction of new built environments. This study used high-throughput targeted sequencing approaches to explore bacterial community acquisition and development throughout the construction of a new build. Microbial sampling spanned from site identification, through the construction process to commissioning and use. Following commissioning of the building, bacterial richness and diversity were significantly reduced (P < 0.001) and community structure was altered (R(2) = 0.14; P = 0.001). Greater longitudinal community stability was observed in outdoor environments than indoor environments. Community flux in indoor environments was associated with human interventions driving environmental selection, which increased 10.4% in indoor environments following commissioning. Increased environmental selection coincided with a 12% reduction in outdoor community influence on indoor microbiomes (P = 2.00 × 10(–15)). Indoor communities became significantly enriched with human associated genera including Escherichia, Pseudomonas, and Klebsiella spp. These data represent the first to characterize the initial assembly of bacterial communities in built environments and will inform future studies aiming to modulate built environment microbiota. Nature Publishing Group UK 2023-09-22 /pmc/articles/PMC10516947/ /pubmed/37740013 http://dx.doi.org/10.1038/s41598-023-42427-0 Text en © The Author(s) 2023 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 Young, Gregory R. Sherry, Angela Smith, Darren L. Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title | Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title_full | Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title_fullStr | Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title_full_unstemmed | Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title_short | Built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
title_sort | built environment microbiomes transition from outdoor to human-associated communities after construction and commissioning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516947/ https://www.ncbi.nlm.nih.gov/pubmed/37740013 http://dx.doi.org/10.1038/s41598-023-42427-0 |
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