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Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure

Good hygiene, in both health care and the community, is central to containing the rise of antibiotic resistance, as well as to infection control more generally. But despite the well-known importance, the ecological mechanisms by which hygiene (or other transmission control measures) affect the evolu...

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Autores principales: Aspenberg, Magnus, Maad Sasane, Sara, Nilsson, Fredrik, Brown, Sam P, Wollein Waldetoft, Kristofer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847546/
https://www.ncbi.nlm.nih.gov/pubmed/36687161
http://dx.doi.org/10.1093/emph/eoac038
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author Aspenberg, Magnus
Maad Sasane, Sara
Nilsson, Fredrik
Brown, Sam P
Wollein Waldetoft, Kristofer
author_facet Aspenberg, Magnus
Maad Sasane, Sara
Nilsson, Fredrik
Brown, Sam P
Wollein Waldetoft, Kristofer
author_sort Aspenberg, Magnus
collection PubMed
description Good hygiene, in both health care and the community, is central to containing the rise of antibiotic resistance, as well as to infection control more generally. But despite the well-known importance, the ecological mechanisms by which hygiene (or other transmission control measures) affect the evolution of resistance remain to be elucidated. Using metacommunity ecology theory, we here propose that hygiene attenuates the effect of antibiotic selection pressure. Specifically, we predict that hygiene limits the scope for antibiotics to induce competitive release of resistant bacteria within treated hosts, and that this is due to an effect of hygiene on the distribution of resistant and sensitive strains in the host population. We show this in a mathematical model of bacterial metacommunity dynamics, and test the results against data on antibiotic resistance, antibiotic treatment, and the use of alcohol-based hand rub in long-term care facilities. The data are consistent with hand rub use attenuating the resistance promoting effect of antibiotic treatment. Our results underscore the importance of hygiene, and point to a concrete way to weaken the link between antibiotic use and increasing resistance.
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spelling pubmed-98475462023-01-20 Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure Aspenberg, Magnus Maad Sasane, Sara Nilsson, Fredrik Brown, Sam P Wollein Waldetoft, Kristofer Evol Med Public Health Original Research Article Good hygiene, in both health care and the community, is central to containing the rise of antibiotic resistance, as well as to infection control more generally. But despite the well-known importance, the ecological mechanisms by which hygiene (or other transmission control measures) affect the evolution of resistance remain to be elucidated. Using metacommunity ecology theory, we here propose that hygiene attenuates the effect of antibiotic selection pressure. Specifically, we predict that hygiene limits the scope for antibiotics to induce competitive release of resistant bacteria within treated hosts, and that this is due to an effect of hygiene on the distribution of resistant and sensitive strains in the host population. We show this in a mathematical model of bacterial metacommunity dynamics, and test the results against data on antibiotic resistance, antibiotic treatment, and the use of alcohol-based hand rub in long-term care facilities. The data are consistent with hand rub use attenuating the resistance promoting effect of antibiotic treatment. Our results underscore the importance of hygiene, and point to a concrete way to weaken the link between antibiotic use and increasing resistance. Oxford University Press 2023-01-18 /pmc/articles/PMC9847546/ /pubmed/36687161 http://dx.doi.org/10.1093/emph/eoac038 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Aspenberg, Magnus
Maad Sasane, Sara
Nilsson, Fredrik
Brown, Sam P
Wollein Waldetoft, Kristofer
Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title_full Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title_fullStr Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title_full_unstemmed Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title_short Hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
title_sort hygiene may attenuate selection for antibiotic resistance by changing microbial community structure
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847546/
https://www.ncbi.nlm.nih.gov/pubmed/36687161
http://dx.doi.org/10.1093/emph/eoac038
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