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Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions

BACKGROUND: Large-scale implementation of Indoor Residual Spraying and Insecticide Treated Nets has been implemented in Plateau Department, Benin between 2011 and 2014. The purpose of this study was to monitor the frequency and mechanisms of pyrethroid resistance in malaria vectors following the imp...

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Autores principales: Yahouédo, Gildas A., Cornelie, Sylvie, Djègbè, Innocent, Ahlonsou, Justine, Aboubakar, Sidick, Soares, Christophe, Akogbéto, Martin, Corbel, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932690/
https://www.ncbi.nlm.nih.gov/pubmed/27378358
http://dx.doi.org/10.1186/s13071-016-1661-8
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author Yahouédo, Gildas A.
Cornelie, Sylvie
Djègbè, Innocent
Ahlonsou, Justine
Aboubakar, Sidick
Soares, Christophe
Akogbéto, Martin
Corbel, Vincent
author_facet Yahouédo, Gildas A.
Cornelie, Sylvie
Djègbè, Innocent
Ahlonsou, Justine
Aboubakar, Sidick
Soares, Christophe
Akogbéto, Martin
Corbel, Vincent
author_sort Yahouédo, Gildas A.
collection PubMed
description BACKGROUND: Large-scale implementation of Indoor Residual Spraying and Insecticide Treated Nets has been implemented in Plateau Department, Benin between 2011 and 2014. The purpose of this study was to monitor the frequency and mechanisms of pyrethroid resistance in malaria vectors following the implementation of vector control tools for malaria prevention. METHODS: Anopheles larvae were collected in 13 villages twice a year from 2012 to 2014. WHO tube tests were used to assess the phenotypic resistance of each population to 0.05 % deltamethrin. Sibling species within Anopheles gambiae complex were identified by PCR techniques. Taqman and biochemical assays were performed to identify the presence of kdr mutations in individual mosquitoes and to detect any increase in the activity of enzymes putatively involved in insecticide metabolism (oxidases, esterase and glutathione-S-transferases). Quantitative real time PCR was used to measure the expression of three metabolic genes involved in pyrethroid resistance (CYP6P3, CYP6M2 and GSTD3). RESULTS: Anopheles populations showed < 90 % mortality to deltamethrin in all villages and at all time points. The 1014 F kdr allele frequency was close to fixation (> 0.9) over the sampling periods in both An. gambiae and An. coluzzii. Biochemical assays showed higher activities of alpha esterase and GST in field malaria vector populations compared to susceptible mosquitoes. qPCR assays showed a significant increase of CYP6P3, CYP6M2 GSTD3 expression in An. gambiae after a three-year implementation of LLINs. CONCLUSION: The study confirmed that deltamethrin resistance is widespread in malaria vectors in Southern Benin. We suspect that the increase in deltamethrin resistance between 2012 and 2014 resulted from an increased expression of metabolic detoxification genes (CYP6M2 and CYP6P3) rather than from kdr mutations. It is urgent to evaluate further the impact of metabolic resistance on the efficacy of vector control interventions using pyrethroid insecticides.
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spelling pubmed-49326902016-07-06 Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions Yahouédo, Gildas A. Cornelie, Sylvie Djègbè, Innocent Ahlonsou, Justine Aboubakar, Sidick Soares, Christophe Akogbéto, Martin Corbel, Vincent Parasit Vectors Research BACKGROUND: Large-scale implementation of Indoor Residual Spraying and Insecticide Treated Nets has been implemented in Plateau Department, Benin between 2011 and 2014. The purpose of this study was to monitor the frequency and mechanisms of pyrethroid resistance in malaria vectors following the implementation of vector control tools for malaria prevention. METHODS: Anopheles larvae were collected in 13 villages twice a year from 2012 to 2014. WHO tube tests were used to assess the phenotypic resistance of each population to 0.05 % deltamethrin. Sibling species within Anopheles gambiae complex were identified by PCR techniques. Taqman and biochemical assays were performed to identify the presence of kdr mutations in individual mosquitoes and to detect any increase in the activity of enzymes putatively involved in insecticide metabolism (oxidases, esterase and glutathione-S-transferases). Quantitative real time PCR was used to measure the expression of three metabolic genes involved in pyrethroid resistance (CYP6P3, CYP6M2 and GSTD3). RESULTS: Anopheles populations showed < 90 % mortality to deltamethrin in all villages and at all time points. The 1014 F kdr allele frequency was close to fixation (> 0.9) over the sampling periods in both An. gambiae and An. coluzzii. Biochemical assays showed higher activities of alpha esterase and GST in field malaria vector populations compared to susceptible mosquitoes. qPCR assays showed a significant increase of CYP6P3, CYP6M2 GSTD3 expression in An. gambiae after a three-year implementation of LLINs. CONCLUSION: The study confirmed that deltamethrin resistance is widespread in malaria vectors in Southern Benin. We suspect that the increase in deltamethrin resistance between 2012 and 2014 resulted from an increased expression of metabolic detoxification genes (CYP6M2 and CYP6P3) rather than from kdr mutations. It is urgent to evaluate further the impact of metabolic resistance on the efficacy of vector control interventions using pyrethroid insecticides. BioMed Central 2016-07-04 /pmc/articles/PMC4932690/ /pubmed/27378358 http://dx.doi.org/10.1186/s13071-016-1661-8 Text en © The Author(s). 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
Yahouédo, Gildas A.
Cornelie, Sylvie
Djègbè, Innocent
Ahlonsou, Justine
Aboubakar, Sidick
Soares, Christophe
Akogbéto, Martin
Corbel, Vincent
Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title_full Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title_fullStr Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title_full_unstemmed Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title_short Dynamics of pyrethroid resistance in malaria vectors in southern Benin following a large scale implementation of vector control interventions
title_sort dynamics of pyrethroid resistance in malaria vectors in southern benin following a large scale implementation of vector control interventions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932690/
https://www.ncbi.nlm.nih.gov/pubmed/27378358
http://dx.doi.org/10.1186/s13071-016-1661-8
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