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Controlling infectious disease through the targeted manipulation of contact network structure
Individuals in human and animal populations are linked through dynamic contact networks with characteristic structural features that drive the epidemiology of directly transmissible infectious diseases. Using animal movement data from the British cattle industry as an example, this analysis explores...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728197/ https://www.ncbi.nlm.nih.gov/pubmed/26342238 http://dx.doi.org/10.1016/j.epidem.2015.02.008 |
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author | Gates, M. Carolyn Woolhouse, Mark E.J. |
author_facet | Gates, M. Carolyn Woolhouse, Mark E.J. |
author_sort | Gates, M. Carolyn |
collection | PubMed |
description | Individuals in human and animal populations are linked through dynamic contact networks with characteristic structural features that drive the epidemiology of directly transmissible infectious diseases. Using animal movement data from the British cattle industry as an example, this analysis explores whether disease dynamics can be altered by placing targeted restrictions on contact formation to reconfigure network topology. This was accomplished using a simple network generation algorithm that combined configuration wiring with stochastic block modelling techniques to preserve the weighted in- and out-degree of individual nodes (farms) as well as key demographic characteristics of the individual network connections (movement date, livestock market, and animal production type). We then tested a control strategy based on introducing additional constraints into the network generation algorithm to prevent farms with a high in-degree from selling cattle to farms with a high out-degree as these particular network connections are predicted to have a disproportionately strong role in spreading disease. Results from simple dynamic disease simulation models predicted significantly lower endemic disease prevalences on the trade restricted networks compared to the baseline generated networks. As expected, the relative magnitude of the predicted changes in endemic prevalence was greater for diseases with short infectious periods and low transmission probabilities. Overall, our study findings demonstrate that there is significant potential for controlling multiple infectious diseases simultaneously by manipulating networks to have more epidemiologically favourable topological configurations. Further research is needed to determine whether the economic and social benefits of controlling disease can justify the costs of restricting contact formation. |
format | Online Article Text |
id | pubmed-4728197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-47281972016-02-22 Controlling infectious disease through the targeted manipulation of contact network structure Gates, M. Carolyn Woolhouse, Mark E.J. Epidemics Article Individuals in human and animal populations are linked through dynamic contact networks with characteristic structural features that drive the epidemiology of directly transmissible infectious diseases. Using animal movement data from the British cattle industry as an example, this analysis explores whether disease dynamics can be altered by placing targeted restrictions on contact formation to reconfigure network topology. This was accomplished using a simple network generation algorithm that combined configuration wiring with stochastic block modelling techniques to preserve the weighted in- and out-degree of individual nodes (farms) as well as key demographic characteristics of the individual network connections (movement date, livestock market, and animal production type). We then tested a control strategy based on introducing additional constraints into the network generation algorithm to prevent farms with a high in-degree from selling cattle to farms with a high out-degree as these particular network connections are predicted to have a disproportionately strong role in spreading disease. Results from simple dynamic disease simulation models predicted significantly lower endemic disease prevalences on the trade restricted networks compared to the baseline generated networks. As expected, the relative magnitude of the predicted changes in endemic prevalence was greater for diseases with short infectious periods and low transmission probabilities. Overall, our study findings demonstrate that there is significant potential for controlling multiple infectious diseases simultaneously by manipulating networks to have more epidemiologically favourable topological configurations. Further research is needed to determine whether the economic and social benefits of controlling disease can justify the costs of restricting contact formation. Elsevier 2015-09 /pmc/articles/PMC4728197/ /pubmed/26342238 http://dx.doi.org/10.1016/j.epidem.2015.02.008 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gates, M. Carolyn Woolhouse, Mark E.J. Controlling infectious disease through the targeted manipulation of contact network structure |
title | Controlling infectious disease through the targeted manipulation of contact network structure |
title_full | Controlling infectious disease through the targeted manipulation of contact network structure |
title_fullStr | Controlling infectious disease through the targeted manipulation of contact network structure |
title_full_unstemmed | Controlling infectious disease through the targeted manipulation of contact network structure |
title_short | Controlling infectious disease through the targeted manipulation of contact network structure |
title_sort | controlling infectious disease through the targeted manipulation of contact network structure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728197/ https://www.ncbi.nlm.nih.gov/pubmed/26342238 http://dx.doi.org/10.1016/j.epidem.2015.02.008 |
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