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Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections
Antibiotic-resistant infections are a growing threat to human health, but basic features of the eco-evolutionary dynamics remain unexplained. Most prominently, there is no clear mechanism for the long-term coexistence of both drug-sensitive and resistant strains at intermediate levels, a ubiquitous...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365476/ https://www.ncbi.nlm.nih.gov/pubmed/32628660 http://dx.doi.org/10.1371/journal.pcbi.1008010 |
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author | Krieger, Madison S. Denison, Carson E. Anderson, Thayer L. Nowak, Martin A. Hill, Alison L. |
author_facet | Krieger, Madison S. Denison, Carson E. Anderson, Thayer L. Nowak, Martin A. Hill, Alison L. |
author_sort | Krieger, Madison S. |
collection | PubMed |
description | Antibiotic-resistant infections are a growing threat to human health, but basic features of the eco-evolutionary dynamics remain unexplained. Most prominently, there is no clear mechanism for the long-term coexistence of both drug-sensitive and resistant strains at intermediate levels, a ubiquitous pattern seen in surveillance data. Here we show that accounting for structured or spatially-heterogeneous host populations and variability in antibiotic consumption can lead to persistent coexistence over a wide range of treatment coverages, drug efficacies, costs of resistance, and mixing patterns. Moreover, this mechanism can explain other puzzling spatiotemporal features of drug-resistance epidemiology that have received less attention, such as large differences in the prevalence of resistance between geographical regions with similar antibiotic consumption or that neighbor one another. We find that the same amount of antibiotic use can lead to very different levels of resistance depending on how treatment is distributed in a transmission network. We also identify parameter regimes in which population structure alone cannot support coexistence, suggesting the need for other mechanisms to explain the epidemiology of antibiotic resistance. Our analysis identifies key features of host population structure that can be used to assess resistance risk and highlights the need to include spatial or demographic heterogeneity in models to guide resistance management. |
format | Online Article Text |
id | pubmed-7365476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73654762020-07-27 Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections Krieger, Madison S. Denison, Carson E. Anderson, Thayer L. Nowak, Martin A. Hill, Alison L. PLoS Comput Biol Research Article Antibiotic-resistant infections are a growing threat to human health, but basic features of the eco-evolutionary dynamics remain unexplained. Most prominently, there is no clear mechanism for the long-term coexistence of both drug-sensitive and resistant strains at intermediate levels, a ubiquitous pattern seen in surveillance data. Here we show that accounting for structured or spatially-heterogeneous host populations and variability in antibiotic consumption can lead to persistent coexistence over a wide range of treatment coverages, drug efficacies, costs of resistance, and mixing patterns. Moreover, this mechanism can explain other puzzling spatiotemporal features of drug-resistance epidemiology that have received less attention, such as large differences in the prevalence of resistance between geographical regions with similar antibiotic consumption or that neighbor one another. We find that the same amount of antibiotic use can lead to very different levels of resistance depending on how treatment is distributed in a transmission network. We also identify parameter regimes in which population structure alone cannot support coexistence, suggesting the need for other mechanisms to explain the epidemiology of antibiotic resistance. Our analysis identifies key features of host population structure that can be used to assess resistance risk and highlights the need to include spatial or demographic heterogeneity in models to guide resistance management. Public Library of Science 2020-07-06 /pmc/articles/PMC7365476/ /pubmed/32628660 http://dx.doi.org/10.1371/journal.pcbi.1008010 Text en © 2020 Krieger et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Krieger, Madison S. Denison, Carson E. Anderson, Thayer L. Nowak, Martin A. Hill, Alison L. Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title | Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title_full | Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title_fullStr | Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title_full_unstemmed | Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title_short | Population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
title_sort | population structure across scales facilitates coexistence and spatial heterogeneity of antibiotic-resistant infections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7365476/ https://www.ncbi.nlm.nih.gov/pubmed/32628660 http://dx.doi.org/10.1371/journal.pcbi.1008010 |
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