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Associated patterns of insecticide resistance in field populations of malaria vectors across Africa
The development of insecticide resistance in African malaria vectors threatens the continued efficacy of important vector control methods that rely on a limited set of insecticides. To understand the operational significance of resistance we require quantitative information about levels of resistanc...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003363/ https://www.ncbi.nlm.nih.gov/pubmed/29784773 http://dx.doi.org/10.1073/pnas.1801826115 |
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author | Hancock, Penelope A. Wiebe, Antoinette Gleave, Katherine A. Bhatt, Samir Cameron, Ewan Trett, Anna Weetman, David Smith, David L. Hemingway, Janet Coleman, Michael Gething, Peter W. Moyes, Catherine L. |
author_facet | Hancock, Penelope A. Wiebe, Antoinette Gleave, Katherine A. Bhatt, Samir Cameron, Ewan Trett, Anna Weetman, David Smith, David L. Hemingway, Janet Coleman, Michael Gething, Peter W. Moyes, Catherine L. |
author_sort | Hancock, Penelope A. |
collection | PubMed |
description | The development of insecticide resistance in African malaria vectors threatens the continued efficacy of important vector control methods that rely on a limited set of insecticides. To understand the operational significance of resistance we require quantitative information about levels of resistance in field populations to the suite of vector control insecticides. Estimation of resistance is complicated by the sparsity of observations in field populations, variation in resistance over time and space at local and regional scales, and cross-resistance between different insecticide types. Using observations of the prevalence of resistance in mosquito species from the Anopheles gambiae complex sampled from 1,183 locations throughout Africa, we applied Bayesian geostatistical models to quantify patterns of covariation in resistance phenotypes across different insecticides. For resistance to the three pyrethroids tested, deltamethrin, permethrin, and λ-cyhalothrin, we found consistent forms of covariation across sub-Saharan Africa and covariation between resistance to these pyrethroids and resistance to DDT. We found no evidence of resistance interactions between carbamate and organophosphate insecticides or between these insecticides and those from other classes. For pyrethroids and DDT we found significant associations between predicted mean resistance and the observed frequency of kdr mutations in the Vgsc gene in field mosquito samples, with DDT showing the strongest association. These results improve our capacity to understand and predict resistance patterns throughout Africa and can guide the development of monitoring strategies. |
format | Online Article Text |
id | pubmed-6003363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-60033632018-06-18 Associated patterns of insecticide resistance in field populations of malaria vectors across Africa Hancock, Penelope A. Wiebe, Antoinette Gleave, Katherine A. Bhatt, Samir Cameron, Ewan Trett, Anna Weetman, David Smith, David L. Hemingway, Janet Coleman, Michael Gething, Peter W. Moyes, Catherine L. Proc Natl Acad Sci U S A Biological Sciences The development of insecticide resistance in African malaria vectors threatens the continued efficacy of important vector control methods that rely on a limited set of insecticides. To understand the operational significance of resistance we require quantitative information about levels of resistance in field populations to the suite of vector control insecticides. Estimation of resistance is complicated by the sparsity of observations in field populations, variation in resistance over time and space at local and regional scales, and cross-resistance between different insecticide types. Using observations of the prevalence of resistance in mosquito species from the Anopheles gambiae complex sampled from 1,183 locations throughout Africa, we applied Bayesian geostatistical models to quantify patterns of covariation in resistance phenotypes across different insecticides. For resistance to the three pyrethroids tested, deltamethrin, permethrin, and λ-cyhalothrin, we found consistent forms of covariation across sub-Saharan Africa and covariation between resistance to these pyrethroids and resistance to DDT. We found no evidence of resistance interactions between carbamate and organophosphate insecticides or between these insecticides and those from other classes. For pyrethroids and DDT we found significant associations between predicted mean resistance and the observed frequency of kdr mutations in the Vgsc gene in field mosquito samples, with DDT showing the strongest association. These results improve our capacity to understand and predict resistance patterns throughout Africa and can guide the development of monitoring strategies. National Academy of Sciences 2018-06-05 2018-05-21 /pmc/articles/PMC6003363/ /pubmed/29784773 http://dx.doi.org/10.1073/pnas.1801826115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Hancock, Penelope A. Wiebe, Antoinette Gleave, Katherine A. Bhatt, Samir Cameron, Ewan Trett, Anna Weetman, David Smith, David L. Hemingway, Janet Coleman, Michael Gething, Peter W. Moyes, Catherine L. Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title | Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title_full | Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title_fullStr | Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title_full_unstemmed | Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title_short | Associated patterns of insecticide resistance in field populations of malaria vectors across Africa |
title_sort | associated patterns of insecticide resistance in field populations of malaria vectors across africa |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003363/ https://www.ncbi.nlm.nih.gov/pubmed/29784773 http://dx.doi.org/10.1073/pnas.1801826115 |
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