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Predictive analysis across spatial scales links zoonotic malaria to deforestation

The complex transmission ecologies of vector-borne and zoonotic diseases pose challenges to their control, especially in changing landscapes. Human incidence of zoonotic malaria (Plasmodium knowlesi) is associated with deforestation although mechanisms are unknown. Here, a novel application of a met...

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Autores principales: Brock, Patrick M., Fornace, Kimberly M., Grigg, Matthew J., Anstey, Nicholas M., William, Timothy, Cox, Jon, Drakeley, Chris J., Ferguson, Heather M., Kao, Rowland R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367187/
https://www.ncbi.nlm.nih.gov/pubmed/30963872
http://dx.doi.org/10.1098/rspb.2018.2351
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author Brock, Patrick M.
Fornace, Kimberly M.
Grigg, Matthew J.
Anstey, Nicholas M.
William, Timothy
Cox, Jon
Drakeley, Chris J.
Ferguson, Heather M.
Kao, Rowland R.
author_facet Brock, Patrick M.
Fornace, Kimberly M.
Grigg, Matthew J.
Anstey, Nicholas M.
William, Timothy
Cox, Jon
Drakeley, Chris J.
Ferguson, Heather M.
Kao, Rowland R.
author_sort Brock, Patrick M.
collection PubMed
description The complex transmission ecologies of vector-borne and zoonotic diseases pose challenges to their control, especially in changing landscapes. Human incidence of zoonotic malaria (Plasmodium knowlesi) is associated with deforestation although mechanisms are unknown. Here, a novel application of a method for predicting disease occurrence that combines machine learning and statistics is used to identify the key spatial scales that define the relationship between zoonotic malaria cases and environmental change. Using data from satellite imagery, a case–control study, and a cross-sectional survey, predictive models of household-level occurrence of P. knowlesi were fitted with 16 variables summarized at 11 spatial scales simultaneously. The method identified a strong and well-defined peak of predictive influence of the proportion of cleared land within 1 km of households on P. knowlesi occurrence. Aspect (1 and 2 km), slope (0.5 km) and canopy regrowth (0.5 km) were important at small scales. By contrast, fragmentation of deforested areas influenced P. knowlesi occurrence probability most strongly at large scales (4 and 5 km). The identification of these spatial scales narrows the field of plausible mechanisms that connect land use change and P. knowlesi, allowing for the refinement of disease occurrence predictions and the design of spatially-targeted interventions.
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spelling pubmed-63671872019-02-22 Predictive analysis across spatial scales links zoonotic malaria to deforestation Brock, Patrick M. Fornace, Kimberly M. Grigg, Matthew J. Anstey, Nicholas M. William, Timothy Cox, Jon Drakeley, Chris J. Ferguson, Heather M. Kao, Rowland R. Proc Biol Sci Ecology The complex transmission ecologies of vector-borne and zoonotic diseases pose challenges to their control, especially in changing landscapes. Human incidence of zoonotic malaria (Plasmodium knowlesi) is associated with deforestation although mechanisms are unknown. Here, a novel application of a method for predicting disease occurrence that combines machine learning and statistics is used to identify the key spatial scales that define the relationship between zoonotic malaria cases and environmental change. Using data from satellite imagery, a case–control study, and a cross-sectional survey, predictive models of household-level occurrence of P. knowlesi were fitted with 16 variables summarized at 11 spatial scales simultaneously. The method identified a strong and well-defined peak of predictive influence of the proportion of cleared land within 1 km of households on P. knowlesi occurrence. Aspect (1 and 2 km), slope (0.5 km) and canopy regrowth (0.5 km) were important at small scales. By contrast, fragmentation of deforested areas influenced P. knowlesi occurrence probability most strongly at large scales (4 and 5 km). The identification of these spatial scales narrows the field of plausible mechanisms that connect land use change and P. knowlesi, allowing for the refinement of disease occurrence predictions and the design of spatially-targeted interventions. The Royal Society 2019-01-16 2019-01-16 /pmc/articles/PMC6367187/ /pubmed/30963872 http://dx.doi.org/10.1098/rspb.2018.2351 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology
Brock, Patrick M.
Fornace, Kimberly M.
Grigg, Matthew J.
Anstey, Nicholas M.
William, Timothy
Cox, Jon
Drakeley, Chris J.
Ferguson, Heather M.
Kao, Rowland R.
Predictive analysis across spatial scales links zoonotic malaria to deforestation
title Predictive analysis across spatial scales links zoonotic malaria to deforestation
title_full Predictive analysis across spatial scales links zoonotic malaria to deforestation
title_fullStr Predictive analysis across spatial scales links zoonotic malaria to deforestation
title_full_unstemmed Predictive analysis across spatial scales links zoonotic malaria to deforestation
title_short Predictive analysis across spatial scales links zoonotic malaria to deforestation
title_sort predictive analysis across spatial scales links zoonotic malaria to deforestation
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367187/
https://www.ncbi.nlm.nih.gov/pubmed/30963872
http://dx.doi.org/10.1098/rspb.2018.2351
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