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Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring

BACKGROUND: Indoor residual spraying (IRS) and long-lasting insecticidal nets (LLINs) remain the cornerstones of malaria vector control. However, the development of insecticide resistance and its implications for operational failure of preventative strategies are of concern. The aim of this study wa...

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Autores principales: Messenger, Louisa A., Shililu, Josephat, Irish, Seth R., Anshebo, Gedeon Yohannes, Tesfaye, Alemayehu Getachew, Ye-Ebiyo, Yemane, Chibsa, Sheleme, Dengela, Dereje, Dissanayake, Gunawardena, Kebede, Estifanos, Zemene, Endalew, Asale, Abebe, Yohannes, Mekonnen, Taffese, Hiwot Solomon, George, Kristen, Fornadel, Christen, Seyoum, Aklilu, Wirtz, Robert A., Yewhalaw, Delenasaw
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694167/
https://www.ncbi.nlm.nih.gov/pubmed/29151024
http://dx.doi.org/10.1186/s12936-017-2115-2
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author Messenger, Louisa A.
Shililu, Josephat
Irish, Seth R.
Anshebo, Gedeon Yohannes
Tesfaye, Alemayehu Getachew
Ye-Ebiyo, Yemane
Chibsa, Sheleme
Dengela, Dereje
Dissanayake, Gunawardena
Kebede, Estifanos
Zemene, Endalew
Asale, Abebe
Yohannes, Mekonnen
Taffese, Hiwot Solomon
George, Kristen
Fornadel, Christen
Seyoum, Aklilu
Wirtz, Robert A.
Yewhalaw, Delenasaw
author_facet Messenger, Louisa A.
Shililu, Josephat
Irish, Seth R.
Anshebo, Gedeon Yohannes
Tesfaye, Alemayehu Getachew
Ye-Ebiyo, Yemane
Chibsa, Sheleme
Dengela, Dereje
Dissanayake, Gunawardena
Kebede, Estifanos
Zemene, Endalew
Asale, Abebe
Yohannes, Mekonnen
Taffese, Hiwot Solomon
George, Kristen
Fornadel, Christen
Seyoum, Aklilu
Wirtz, Robert A.
Yewhalaw, Delenasaw
author_sort Messenger, Louisa A.
collection PubMed
description BACKGROUND: Indoor residual spraying (IRS) and long-lasting insecticidal nets (LLINs) remain the cornerstones of malaria vector control. However, the development of insecticide resistance and its implications for operational failure of preventative strategies are of concern. The aim of this study was to characterize insecticide resistance among Anopheles arabiensis populations in Ethiopia and describe temporal and spatial patterns of resistance between 2012 and 2016. METHODS: Between 2012 and 2016, resistance status of An. arabiensis was assessed annually during the long rainy seasons in study sites from seven of the nine regions in Ethiopia. Insecticide resistance levels were measured with WHO susceptibility tests and CDC bottle bioassays using insecticides from four chemical classes (organochlorines, pyrethroids, organophosphates and carbamates), with minor variations in insecticides tested and assays conducted between years. In selected sites, CDC synergist assays were performed by pre-exposing mosquitoes to piperonyl butoxide (PBO). In 2015 and 2016, mosquitoes from DDT and deltamethrin bioassays were randomly selected, identified to species-level and screened for knockdown resistance (kdr) by PCR. RESULTS: Intense resistance to DDT and pyrethroids was pervasive across Ethiopia, consistent with historic use of DDT for IRS and concomitant increases in insecticide-treated net coverage over the last 15 years. Longitudinal resistance trends to malathion, bendiocarb, propoxur and pirimiphos-methyl corresponded to shifts in the national insecticide policy. By 2016, resistance to the latter two insecticides had emerged, with the potential to jeopardize future long-term effectiveness of vector control activities in these areas. Between 2015 and 2016, the West African (L1014F) kdr allele was detected in 74.1% (n = 686/926) of specimens, with frequencies ranging from 31 to 100% and 33 to 100% in survivors from DDT and deltamethrin bioassays, respectively. Restoration of mosquito susceptibility, following pre-exposure to PBO, along with a lack of association between kdr allele frequency and An. arabiensis mortality rate, both indicate metabolic and target-site mutation mechanisms are contributing to insecticide resistance. CONCLUSIONS: Data generated by this study will strengthen the National Malaria Control Programme’s insecticide resistance management strategy to safeguard continued efficacy of IRS and other malaria control methods in Ethiopia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-017-2115-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-56941672017-11-27 Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring Messenger, Louisa A. Shililu, Josephat Irish, Seth R. Anshebo, Gedeon Yohannes Tesfaye, Alemayehu Getachew Ye-Ebiyo, Yemane Chibsa, Sheleme Dengela, Dereje Dissanayake, Gunawardena Kebede, Estifanos Zemene, Endalew Asale, Abebe Yohannes, Mekonnen Taffese, Hiwot Solomon George, Kristen Fornadel, Christen Seyoum, Aklilu Wirtz, Robert A. Yewhalaw, Delenasaw Malar J Research BACKGROUND: Indoor residual spraying (IRS) and long-lasting insecticidal nets (LLINs) remain the cornerstones of malaria vector control. However, the development of insecticide resistance and its implications for operational failure of preventative strategies are of concern. The aim of this study was to characterize insecticide resistance among Anopheles arabiensis populations in Ethiopia and describe temporal and spatial patterns of resistance between 2012 and 2016. METHODS: Between 2012 and 2016, resistance status of An. arabiensis was assessed annually during the long rainy seasons in study sites from seven of the nine regions in Ethiopia. Insecticide resistance levels were measured with WHO susceptibility tests and CDC bottle bioassays using insecticides from four chemical classes (organochlorines, pyrethroids, organophosphates and carbamates), with minor variations in insecticides tested and assays conducted between years. In selected sites, CDC synergist assays were performed by pre-exposing mosquitoes to piperonyl butoxide (PBO). In 2015 and 2016, mosquitoes from DDT and deltamethrin bioassays were randomly selected, identified to species-level and screened for knockdown resistance (kdr) by PCR. RESULTS: Intense resistance to DDT and pyrethroids was pervasive across Ethiopia, consistent with historic use of DDT for IRS and concomitant increases in insecticide-treated net coverage over the last 15 years. Longitudinal resistance trends to malathion, bendiocarb, propoxur and pirimiphos-methyl corresponded to shifts in the national insecticide policy. By 2016, resistance to the latter two insecticides had emerged, with the potential to jeopardize future long-term effectiveness of vector control activities in these areas. Between 2015 and 2016, the West African (L1014F) kdr allele was detected in 74.1% (n = 686/926) of specimens, with frequencies ranging from 31 to 100% and 33 to 100% in survivors from DDT and deltamethrin bioassays, respectively. Restoration of mosquito susceptibility, following pre-exposure to PBO, along with a lack of association between kdr allele frequency and An. arabiensis mortality rate, both indicate metabolic and target-site mutation mechanisms are contributing to insecticide resistance. CONCLUSIONS: Data generated by this study will strengthen the National Malaria Control Programme’s insecticide resistance management strategy to safeguard continued efficacy of IRS and other malaria control methods in Ethiopia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-017-2115-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-18 /pmc/articles/PMC5694167/ /pubmed/29151024 http://dx.doi.org/10.1186/s12936-017-2115-2 Text en © The Author(s) 2017 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
Messenger, Louisa A.
Shililu, Josephat
Irish, Seth R.
Anshebo, Gedeon Yohannes
Tesfaye, Alemayehu Getachew
Ye-Ebiyo, Yemane
Chibsa, Sheleme
Dengela, Dereje
Dissanayake, Gunawardena
Kebede, Estifanos
Zemene, Endalew
Asale, Abebe
Yohannes, Mekonnen
Taffese, Hiwot Solomon
George, Kristen
Fornadel, Christen
Seyoum, Aklilu
Wirtz, Robert A.
Yewhalaw, Delenasaw
Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title_full Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title_fullStr Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title_full_unstemmed Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title_short Insecticide resistance in Anopheles arabiensis from Ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
title_sort insecticide resistance in anopheles arabiensis from ethiopia (2012–2016): a nationwide study for insecticide resistance monitoring
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694167/
https://www.ncbi.nlm.nih.gov/pubmed/29151024
http://dx.doi.org/10.1186/s12936-017-2115-2
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