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A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia
BACKGROUND: Murray Valley encephalitis virus (MVEV) is a clinically important virus in Australia responsible for a number of epidemics over the past century. Since there is no vaccine for MVEV, other preventive health measures to curtail its spread must be considered, including the development of pr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730662/ https://www.ncbi.nlm.nih.gov/pubmed/26823368 http://dx.doi.org/10.1186/s12942-016-0036-x |
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author | Ho, Soon Hoe Speldewinde, Peter Cook, Angus |
author_facet | Ho, Soon Hoe Speldewinde, Peter Cook, Angus |
author_sort | Ho, Soon Hoe |
collection | PubMed |
description | BACKGROUND: Murray Valley encephalitis virus (MVEV) is a clinically important virus in Australia responsible for a number of epidemics over the past century. Since there is no vaccine for MVEV, other preventive health measures to curtail its spread must be considered, including the development of predictive risk models and maps to help direct public health interventions. This article aims to support these approaches by presenting a model for assessing MVEV risk in Western Australia (WA). METHODS: A Bayesian Belief Network (BBN) for assessing MVEV risk was developed and used to quantify and map disease risks in WA. The model combined various abiotic, biotic, and anthropogenic factors that might affect the risk of MVEV into a predictive framework, based on the ecology of the major mosquito vector and waterbird hosts of MVEV. It was further refined and tested using retrospective climate data from 4 years (2000, 2003, 2009, and 2011). RESULTS: Implementing the model across WA demonstrated that it could predict locations of human MVEV infection and sentinel animal seroconversion in the 4 years tested with some degree of accuracy. In general, risks are highest in the State’s north and lower in the south. The model predicted that short-term climate change, based on the Intergovernmental Panel on Climate Change’s A1B emissions scenario, would decrease MVEV risks in summer and autumn, largely due to higher temperatures decreasing vector survival. CONCLUSIONS: To our knowledge, this is the first model to use a BBN to quantify MVEV risks in WA. The models and maps developed here may assist public health agencies in preparing for and managing Murray Valley encephalitis in the future. In its current form, the model is knowledge-driven and based on the analysis of potential risk factors that affect the dynamics of MVEV using retrospective data. Further work and additional testing should be carried out to test its validity in future years. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12942-016-0036-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4730662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47306622016-01-29 A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia Ho, Soon Hoe Speldewinde, Peter Cook, Angus Int J Health Geogr Research BACKGROUND: Murray Valley encephalitis virus (MVEV) is a clinically important virus in Australia responsible for a number of epidemics over the past century. Since there is no vaccine for MVEV, other preventive health measures to curtail its spread must be considered, including the development of predictive risk models and maps to help direct public health interventions. This article aims to support these approaches by presenting a model for assessing MVEV risk in Western Australia (WA). METHODS: A Bayesian Belief Network (BBN) for assessing MVEV risk was developed and used to quantify and map disease risks in WA. The model combined various abiotic, biotic, and anthropogenic factors that might affect the risk of MVEV into a predictive framework, based on the ecology of the major mosquito vector and waterbird hosts of MVEV. It was further refined and tested using retrospective climate data from 4 years (2000, 2003, 2009, and 2011). RESULTS: Implementing the model across WA demonstrated that it could predict locations of human MVEV infection and sentinel animal seroconversion in the 4 years tested with some degree of accuracy. In general, risks are highest in the State’s north and lower in the south. The model predicted that short-term climate change, based on the Intergovernmental Panel on Climate Change’s A1B emissions scenario, would decrease MVEV risks in summer and autumn, largely due to higher temperatures decreasing vector survival. CONCLUSIONS: To our knowledge, this is the first model to use a BBN to quantify MVEV risks in WA. The models and maps developed here may assist public health agencies in preparing for and managing Murray Valley encephalitis in the future. In its current form, the model is knowledge-driven and based on the analysis of potential risk factors that affect the dynamics of MVEV using retrospective data. Further work and additional testing should be carried out to test its validity in future years. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12942-016-0036-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-28 /pmc/articles/PMC4730662/ /pubmed/26823368 http://dx.doi.org/10.1186/s12942-016-0036-x Text en © Ho et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ho, Soon Hoe Speldewinde, Peter Cook, Angus A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title | A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title_full | A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title_fullStr | A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title_full_unstemmed | A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title_short | A Bayesian Belief Network for Murray Valley encephalitis virus risk assessment in Western Australia |
title_sort | bayesian belief network for murray valley encephalitis virus risk assessment in western australia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4730662/ https://www.ncbi.nlm.nih.gov/pubmed/26823368 http://dx.doi.org/10.1186/s12942-016-0036-x |
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