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Implications of indoor microbial ecology and evolution on antibiotic resistance
The indoor environment is an important source of microbial exposures for its human occupants. While we naturally want to favor positive health outcomes, built environment design and operation may counter-intuitively favor negative health outcomes, particularly with regard to antibiotic resistance. I...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075925/ https://www.ncbi.nlm.nih.gov/pubmed/31591493 http://dx.doi.org/10.1038/s41370-019-0171-0 |
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author | Ben Maamar, Sarah Hu, Jinglin Hartmann, Erica M. |
author_facet | Ben Maamar, Sarah Hu, Jinglin Hartmann, Erica M. |
author_sort | Ben Maamar, Sarah |
collection | PubMed |
description | The indoor environment is an important source of microbial exposures for its human occupants. While we naturally want to favor positive health outcomes, built environment design and operation may counter-intuitively favor negative health outcomes, particularly with regard to antibiotic resistance. Indoor environments contain microbes from both human and non-human origins, providing a unique venue for microbial interactions, including horizontal gene transfer. Furthermore, stressors present in the built environment could favor the exchange of genetic material in general and the retention of antibiotic resistance genes in particular. Intrinsic and acquired antibiotic resistance both pose a potential threat to human health; these phenomena need to be considered and controlled separately. The presence of both environmental and human-associated microbes, along with their associated antibiotic resistance genes, in the face of stressors, including antimicrobial chemicals, creates a unique opportunity for the undesirable spread of antibiotic resistance. In this review, we summarize studies and findings related to various interactions between human-associated bacteria, environmental bacteria, and built environment conditions, and particularly their relation to antibiotic resistance, aiming to guide “healthy” building design. |
format | Online Article Text |
id | pubmed-8075925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-80759252021-05-06 Implications of indoor microbial ecology and evolution on antibiotic resistance Ben Maamar, Sarah Hu, Jinglin Hartmann, Erica M. J Expo Sci Environ Epidemiol Review Article The indoor environment is an important source of microbial exposures for its human occupants. While we naturally want to favor positive health outcomes, built environment design and operation may counter-intuitively favor negative health outcomes, particularly with regard to antibiotic resistance. Indoor environments contain microbes from both human and non-human origins, providing a unique venue for microbial interactions, including horizontal gene transfer. Furthermore, stressors present in the built environment could favor the exchange of genetic material in general and the retention of antibiotic resistance genes in particular. Intrinsic and acquired antibiotic resistance both pose a potential threat to human health; these phenomena need to be considered and controlled separately. The presence of both environmental and human-associated microbes, along with their associated antibiotic resistance genes, in the face of stressors, including antimicrobial chemicals, creates a unique opportunity for the undesirable spread of antibiotic resistance. In this review, we summarize studies and findings related to various interactions between human-associated bacteria, environmental bacteria, and built environment conditions, and particularly their relation to antibiotic resistance, aiming to guide “healthy” building design. Nature Publishing Group US 2019-10-07 2020 /pmc/articles/PMC8075925/ /pubmed/31591493 http://dx.doi.org/10.1038/s41370-019-0171-0 Text en © The Author(s) 2019. This article is published with open access 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Ben Maamar, Sarah Hu, Jinglin Hartmann, Erica M. Implications of indoor microbial ecology and evolution on antibiotic resistance |
title | Implications of indoor microbial ecology and evolution on antibiotic resistance |
title_full | Implications of indoor microbial ecology and evolution on antibiotic resistance |
title_fullStr | Implications of indoor microbial ecology and evolution on antibiotic resistance |
title_full_unstemmed | Implications of indoor microbial ecology and evolution on antibiotic resistance |
title_short | Implications of indoor microbial ecology and evolution on antibiotic resistance |
title_sort | implications of indoor microbial ecology and evolution on antibiotic resistance |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075925/ https://www.ncbi.nlm.nih.gov/pubmed/31591493 http://dx.doi.org/10.1038/s41370-019-0171-0 |
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