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Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species

BACKGROUND: Resistance in malaria vectors to pyrethroids, the most widely used class of insecticides for malaria vector control, threatens the continued efficacy of vector control tools. Target-site resistance is an important genetic resistance mechanism caused by mutations in the voltage-gated sodi...

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Autores principales: Hancock, Penelope A., Lynd, Amy, Wiebe, Antoinette, Devine, Maria, Essandoh, John, Wat’senga, Francis, Manzambi, Emile Z., Agossa, Fiacre, Donnelly, Martin J., Weetman, David, Moyes, Catherine L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845222/
https://www.ncbi.nlm.nih.gov/pubmed/35164747
http://dx.doi.org/10.1186/s12915-022-01242-1
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author Hancock, Penelope A.
Lynd, Amy
Wiebe, Antoinette
Devine, Maria
Essandoh, John
Wat’senga, Francis
Manzambi, Emile Z.
Agossa, Fiacre
Donnelly, Martin J.
Weetman, David
Moyes, Catherine L.
author_facet Hancock, Penelope A.
Lynd, Amy
Wiebe, Antoinette
Devine, Maria
Essandoh, John
Wat’senga, Francis
Manzambi, Emile Z.
Agossa, Fiacre
Donnelly, Martin J.
Weetman, David
Moyes, Catherine L.
author_sort Hancock, Penelope A.
collection PubMed
description BACKGROUND: Resistance in malaria vectors to pyrethroids, the most widely used class of insecticides for malaria vector control, threatens the continued efficacy of vector control tools. Target-site resistance is an important genetic resistance mechanism caused by mutations in the voltage-gated sodium channel (Vgsc) gene that encodes the pyrethroid target-site. Understanding the geographic distribution of target-site resistance, and temporal trends across different vector species, can inform strategic deployment of vector control tools. RESULTS: We develop a Bayesian statistical spatiotemporal model to interpret species-specific trends in the frequency of the most common resistance mutations, Vgsc-995S and Vgsc-995F, in three major malaria vector species Anopheles gambiae, An. coluzzii, and An. arabiensis over the period 2005–2017. The models are informed by 2418 observations of the frequency of each mutation in field sampled mosquitoes collected from 27 countries spanning western and eastern regions of Africa. For nine selected countries, we develop annual predictive maps which reveal geographically structured patterns of spread of each mutation at regional and continental scales. The results show associations, as well as stark differences, in spread dynamics of the two mutations across the three vector species. The coverage of ITNs was an influential predictor of Vgsc allele frequencies, with modelled relationships between ITN coverage and allele frequencies varying across species and geographic regions. We found that our mapped Vgsc allele frequencies are a significant partial predictor of phenotypic resistance to the pyrethroid deltamethrin in An. gambiae complex populations. CONCLUSIONS: Our predictive maps show how spatiotemporal trends in insecticide target-site resistance mechanisms in African An. gambiae vary across individual vector species and geographic regions. Molecular surveillance of resistance mechanisms will help to predict resistance phenotypes and track their spread. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01242-1.
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spelling pubmed-88452222022-02-16 Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species Hancock, Penelope A. Lynd, Amy Wiebe, Antoinette Devine, Maria Essandoh, John Wat’senga, Francis Manzambi, Emile Z. Agossa, Fiacre Donnelly, Martin J. Weetman, David Moyes, Catherine L. BMC Biol Research Article BACKGROUND: Resistance in malaria vectors to pyrethroids, the most widely used class of insecticides for malaria vector control, threatens the continued efficacy of vector control tools. Target-site resistance is an important genetic resistance mechanism caused by mutations in the voltage-gated sodium channel (Vgsc) gene that encodes the pyrethroid target-site. Understanding the geographic distribution of target-site resistance, and temporal trends across different vector species, can inform strategic deployment of vector control tools. RESULTS: We develop a Bayesian statistical spatiotemporal model to interpret species-specific trends in the frequency of the most common resistance mutations, Vgsc-995S and Vgsc-995F, in three major malaria vector species Anopheles gambiae, An. coluzzii, and An. arabiensis over the period 2005–2017. The models are informed by 2418 observations of the frequency of each mutation in field sampled mosquitoes collected from 27 countries spanning western and eastern regions of Africa. For nine selected countries, we develop annual predictive maps which reveal geographically structured patterns of spread of each mutation at regional and continental scales. The results show associations, as well as stark differences, in spread dynamics of the two mutations across the three vector species. The coverage of ITNs was an influential predictor of Vgsc allele frequencies, with modelled relationships between ITN coverage and allele frequencies varying across species and geographic regions. We found that our mapped Vgsc allele frequencies are a significant partial predictor of phenotypic resistance to the pyrethroid deltamethrin in An. gambiae complex populations. CONCLUSIONS: Our predictive maps show how spatiotemporal trends in insecticide target-site resistance mechanisms in African An. gambiae vary across individual vector species and geographic regions. Molecular surveillance of resistance mechanisms will help to predict resistance phenotypes and track their spread. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01242-1. BioMed Central 2022-02-15 /pmc/articles/PMC8845222/ /pubmed/35164747 http://dx.doi.org/10.1186/s12915-022-01242-1 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Hancock, Penelope A.
Lynd, Amy
Wiebe, Antoinette
Devine, Maria
Essandoh, John
Wat’senga, Francis
Manzambi, Emile Z.
Agossa, Fiacre
Donnelly, Martin J.
Weetman, David
Moyes, Catherine L.
Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title_full Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title_fullStr Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title_full_unstemmed Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title_short Modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in African mosquito malaria vector species
title_sort modelling spatiotemporal trends in the frequency of genetic mutations conferring insecticide target-site resistance in african mosquito malaria vector species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845222/
https://www.ncbi.nlm.nih.gov/pubmed/35164747
http://dx.doi.org/10.1186/s12915-022-01242-1
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