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The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments

BACKGROUND: The use of gene drive systems to manipulate populations of malaria vectors is currently being investigated as a method of malaria control. One potential system uses driving endonuclease genes (DEGs) to spread genes that impose a genetic load. Previously, models have shown that the introd...

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Autores principales: Lambert, Ben, North, Ace, Burt, Austin, Godfray, H. Charles J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885365/
https://www.ncbi.nlm.nih.gov/pubmed/29618367
http://dx.doi.org/10.1186/s12936-018-2259-8
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author Lambert, Ben
North, Ace
Burt, Austin
Godfray, H. Charles J.
author_facet Lambert, Ben
North, Ace
Burt, Austin
Godfray, H. Charles J.
author_sort Lambert, Ben
collection PubMed
description BACKGROUND: The use of gene drive systems to manipulate populations of malaria vectors is currently being investigated as a method of malaria control. One potential system uses driving endonuclease genes (DEGs) to spread genes that impose a genetic load. Previously, models have shown that the introduction of DEG-bearing mosquitoes could suppress or even extinguish vector populations in spatially-heterogeneous environments which were constant over time. In this study, a stochastic spatially-explicit model of mosquito ecology is combined with a rainfall model which enables the generation of a variety of daily precipitation patterns. The model is then used to investigate how releases of a DEG that cause a bias in population sex ratios towards males are affected by seasonal or random rainfall patterns. The parameters of the rainfall model are then fitted using data from Bamako, Mali, and Mbita, Kenya, to evaluate release strategies in similar climatic conditions. RESULTS: In landscapes with abundant resources and large mosquito populations the spread of a DEG is reliable, irrespective of variability in rainfall. This study thus focuses mainly on landscapes with low density mosquito populations where the spread of a DEG may be sensitive to variation in rainfall. It is found that an introduced DEG will spread into its target population more reliably in wet conditions, yet an established DEG will have more impact in dry conditions. In strongly seasonal environments, it is thus preferable to release DEGs at the onset of a wet season to maximize their spread before the following dry season. If the variability in rainfall has a substantial random component, there is a net increase in the probability that a DEG release will lead to population extinction, due to the increased impact of a DEG which manages to establish in these conditions. For Bamako, where annual rainfall patterns are characterized by a long dry season, it is optimal to release a DEG at the start of the wet season, where the population is growing fastest. By contrast release timing is of lower importance for the less seasonal Mbita. CONCLUSION: This analysis suggests that DEG based methods of malaria vector control can be effective in a wide range of climates. In environments with substantial temporal variation in rainfall, careful timing of releases which accounts for the temporal variation in population density can substantially improve the probability of mosquito suppression or extinction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2259-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-58853652018-04-09 The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments Lambert, Ben North, Ace Burt, Austin Godfray, H. Charles J. Malar J Research BACKGROUND: The use of gene drive systems to manipulate populations of malaria vectors is currently being investigated as a method of malaria control. One potential system uses driving endonuclease genes (DEGs) to spread genes that impose a genetic load. Previously, models have shown that the introduction of DEG-bearing mosquitoes could suppress or even extinguish vector populations in spatially-heterogeneous environments which were constant over time. In this study, a stochastic spatially-explicit model of mosquito ecology is combined with a rainfall model which enables the generation of a variety of daily precipitation patterns. The model is then used to investigate how releases of a DEG that cause a bias in population sex ratios towards males are affected by seasonal or random rainfall patterns. The parameters of the rainfall model are then fitted using data from Bamako, Mali, and Mbita, Kenya, to evaluate release strategies in similar climatic conditions. RESULTS: In landscapes with abundant resources and large mosquito populations the spread of a DEG is reliable, irrespective of variability in rainfall. This study thus focuses mainly on landscapes with low density mosquito populations where the spread of a DEG may be sensitive to variation in rainfall. It is found that an introduced DEG will spread into its target population more reliably in wet conditions, yet an established DEG will have more impact in dry conditions. In strongly seasonal environments, it is thus preferable to release DEGs at the onset of a wet season to maximize their spread before the following dry season. If the variability in rainfall has a substantial random component, there is a net increase in the probability that a DEG release will lead to population extinction, due to the increased impact of a DEG which manages to establish in these conditions. For Bamako, where annual rainfall patterns are characterized by a long dry season, it is optimal to release a DEG at the start of the wet season, where the population is growing fastest. By contrast release timing is of lower importance for the less seasonal Mbita. CONCLUSION: This analysis suggests that DEG based methods of malaria vector control can be effective in a wide range of climates. In environments with substantial temporal variation in rainfall, careful timing of releases which accounts for the temporal variation in population density can substantially improve the probability of mosquito suppression or extinction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2259-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-04 /pmc/articles/PMC5885365/ /pubmed/29618367 http://dx.doi.org/10.1186/s12936-018-2259-8 Text en © The Author(s) 2018 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
Lambert, Ben
North, Ace
Burt, Austin
Godfray, H. Charles J.
The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title_full The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title_fullStr The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title_full_unstemmed The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title_short The use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
title_sort use of driving endonuclease genes to suppress mosquito vectors of malaria in temporally variable environments
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5885365/
https://www.ncbi.nlm.nih.gov/pubmed/29618367
http://dx.doi.org/10.1186/s12936-018-2259-8
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