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Asymmetric host movement reshapes local disease dynamics in metapopulations
Understanding how the movement of individuals affects disease dynamics is critical to accurately predicting and responding to the spread of disease in an increasingly interconnected world. In particular, it is not yet known how movement between patches affects local disease dynamics (e.g., whether p...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171740/ https://www.ncbi.nlm.nih.gov/pubmed/35672422 http://dx.doi.org/10.1038/s41598-022-12774-5 |
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author | Michalska-Smith, Matthew VanderWaal, Kimberly Craft, Meggan E. |
author_facet | Michalska-Smith, Matthew VanderWaal, Kimberly Craft, Meggan E. |
author_sort | Michalska-Smith, Matthew |
collection | PubMed |
description | Understanding how the movement of individuals affects disease dynamics is critical to accurately predicting and responding to the spread of disease in an increasingly interconnected world. In particular, it is not yet known how movement between patches affects local disease dynamics (e.g., whether pathogen prevalence remains steady or oscillates through time). Considering a set of small, archetypal metapopulations, we find three surprisingly simple patterns emerge in local disease dynamics following the introduction of movement between patches: (1) movement between identical patches with cyclical pathogen prevalence dampens oscillations in the destination while increasing synchrony between patches; (2) when patches differ from one another in the absence of movement, adding movement allows dynamics to propagate between patches, alternatively stabilizing or destabilizing dynamics in the destination based on the dynamics at the origin; and (3) it is easier for movement to induce cyclical dynamics than to induce a steady-state. Considering these archetypal networks (and the patterns they exemplify) as building blocks of larger, more realistically complex metapopulations provides an avenue for novel insights into the role of host movement on disease dynamics. Moreover, this work demonstrates a framework for future predictive modelling of disease spread in real populations. |
format | Online Article Text |
id | pubmed-9171740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91717402022-06-08 Asymmetric host movement reshapes local disease dynamics in metapopulations Michalska-Smith, Matthew VanderWaal, Kimberly Craft, Meggan E. Sci Rep Article Understanding how the movement of individuals affects disease dynamics is critical to accurately predicting and responding to the spread of disease in an increasingly interconnected world. In particular, it is not yet known how movement between patches affects local disease dynamics (e.g., whether pathogen prevalence remains steady or oscillates through time). Considering a set of small, archetypal metapopulations, we find three surprisingly simple patterns emerge in local disease dynamics following the introduction of movement between patches: (1) movement between identical patches with cyclical pathogen prevalence dampens oscillations in the destination while increasing synchrony between patches; (2) when patches differ from one another in the absence of movement, adding movement allows dynamics to propagate between patches, alternatively stabilizing or destabilizing dynamics in the destination based on the dynamics at the origin; and (3) it is easier for movement to induce cyclical dynamics than to induce a steady-state. Considering these archetypal networks (and the patterns they exemplify) as building blocks of larger, more realistically complex metapopulations provides an avenue for novel insights into the role of host movement on disease dynamics. Moreover, this work demonstrates a framework for future predictive modelling of disease spread in real populations. Nature Publishing Group UK 2022-06-07 /pmc/articles/PMC9171740/ /pubmed/35672422 http://dx.doi.org/10.1038/s41598-022-12774-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Michalska-Smith, Matthew VanderWaal, Kimberly Craft, Meggan E. Asymmetric host movement reshapes local disease dynamics in metapopulations |
title | Asymmetric host movement reshapes local disease dynamics in metapopulations |
title_full | Asymmetric host movement reshapes local disease dynamics in metapopulations |
title_fullStr | Asymmetric host movement reshapes local disease dynamics in metapopulations |
title_full_unstemmed | Asymmetric host movement reshapes local disease dynamics in metapopulations |
title_short | Asymmetric host movement reshapes local disease dynamics in metapopulations |
title_sort | asymmetric host movement reshapes local disease dynamics in metapopulations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171740/ https://www.ncbi.nlm.nih.gov/pubmed/35672422 http://dx.doi.org/10.1038/s41598-022-12774-5 |
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