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Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda

BACKGROUND: The widespread emergence of resistance to pyrethroids is a major threat to the gains made in malaria control. To monitor the presence and possible emergence of resistance against a variety of insecticides used for malaria control in Rwanda, nationwide insecticide resistance surveys were...

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Autores principales: Hakizimana, Emmanuel, Karema, Corine, Munyakanage, Dunia, Iranzi, Gad, Githure, John, Tongren, Jon Eric, Takken, Willem, Binagwaho, Agnes, Koenraadt, Constantianus J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134262/
https://www.ncbi.nlm.nih.gov/pubmed/27905919
http://dx.doi.org/10.1186/s12936-016-1618-6
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author Hakizimana, Emmanuel
Karema, Corine
Munyakanage, Dunia
Iranzi, Gad
Githure, John
Tongren, Jon Eric
Takken, Willem
Binagwaho, Agnes
Koenraadt, Constantianus J. M.
author_facet Hakizimana, Emmanuel
Karema, Corine
Munyakanage, Dunia
Iranzi, Gad
Githure, John
Tongren, Jon Eric
Takken, Willem
Binagwaho, Agnes
Koenraadt, Constantianus J. M.
author_sort Hakizimana, Emmanuel
collection PubMed
description BACKGROUND: The widespread emergence of resistance to pyrethroids is a major threat to the gains made in malaria control. To monitor the presence and possible emergence of resistance against a variety of insecticides used for malaria control in Rwanda, nationwide insecticide resistance surveys were conducted in 2011 and 2013. METHODS: Larvae of Anopheles gambiae sensu lato mosquitoes were collected in 12 sentinel sites throughout Rwanda. These were reared to adults and analysed for knock-down and mortality using WHO insecticide test papers with standard diagnostic doses of the recommended insecticides. A sub-sample of tested specimens was analysed for the presence of knockdown resistance (kdr) mutations. RESULTS: A total of 14,311 mosquitoes were tested and from a sample of 1406 specimens, 1165 (82.9%) were identified as Anopheles arabiensis and 241 (17.1%) as Anopheles gambiae sensu stricto. Mortality results indicated a significant increase in resistance to lambda-cyhalothrin from 2011 to 2013 in 83% of the sites, permethrin in 25% of the sites, deltamethrin in 25% of the sites and DDT in 50% of the sites. Mosquitoes from 83% of the sites showed full susceptibility to bendiocarb and 17% of sites were suspected to harbour resistance that requires further confirmation. No resistance was observed to fenitrothion in all study sites during the entire survey. The kdr genotype results in An. gambiae s.s. showed that 67 (50%) possessed susceptibility (SS) alleles, while 35 (26.1%) and 32 (23.9%) mosquitoes had heterozygous (RS) and homozygous (RR) alleles, respectively. Of the 591 An. arabiensis genotyped, 425 (71.9%) possessed homozygous (SS) alleles while 158 (26.7%) and 8 (1.4%) had heterozygous (RS) and homozygous (RR) alleles, respectively. Metabolic resistance involving oxidase enzymes was also detected using the synergist PBO. CONCLUSION: This is the first nationwide study of insecticide resistance in malaria vectors in Rwanda. It shows the gradual increase of insecticide resistance to pyrethroids (lambda-cyhalothrin, deltamethrin, permethrin) and organochlorines (DDT) and the large presence of target site insensitivity. The results demonstrate the need for Rwanda to expand monitoring for insecticide resistance including further metabolic resistance testing and implement an insecticide resistance management strategy to sustain the gains made in malaria control.
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spelling pubmed-51342622016-12-15 Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda Hakizimana, Emmanuel Karema, Corine Munyakanage, Dunia Iranzi, Gad Githure, John Tongren, Jon Eric Takken, Willem Binagwaho, Agnes Koenraadt, Constantianus J. M. Malar J Research BACKGROUND: The widespread emergence of resistance to pyrethroids is a major threat to the gains made in malaria control. To monitor the presence and possible emergence of resistance against a variety of insecticides used for malaria control in Rwanda, nationwide insecticide resistance surveys were conducted in 2011 and 2013. METHODS: Larvae of Anopheles gambiae sensu lato mosquitoes were collected in 12 sentinel sites throughout Rwanda. These were reared to adults and analysed for knock-down and mortality using WHO insecticide test papers with standard diagnostic doses of the recommended insecticides. A sub-sample of tested specimens was analysed for the presence of knockdown resistance (kdr) mutations. RESULTS: A total of 14,311 mosquitoes were tested and from a sample of 1406 specimens, 1165 (82.9%) were identified as Anopheles arabiensis and 241 (17.1%) as Anopheles gambiae sensu stricto. Mortality results indicated a significant increase in resistance to lambda-cyhalothrin from 2011 to 2013 in 83% of the sites, permethrin in 25% of the sites, deltamethrin in 25% of the sites and DDT in 50% of the sites. Mosquitoes from 83% of the sites showed full susceptibility to bendiocarb and 17% of sites were suspected to harbour resistance that requires further confirmation. No resistance was observed to fenitrothion in all study sites during the entire survey. The kdr genotype results in An. gambiae s.s. showed that 67 (50%) possessed susceptibility (SS) alleles, while 35 (26.1%) and 32 (23.9%) mosquitoes had heterozygous (RS) and homozygous (RR) alleles, respectively. Of the 591 An. arabiensis genotyped, 425 (71.9%) possessed homozygous (SS) alleles while 158 (26.7%) and 8 (1.4%) had heterozygous (RS) and homozygous (RR) alleles, respectively. Metabolic resistance involving oxidase enzymes was also detected using the synergist PBO. CONCLUSION: This is the first nationwide study of insecticide resistance in malaria vectors in Rwanda. It shows the gradual increase of insecticide resistance to pyrethroids (lambda-cyhalothrin, deltamethrin, permethrin) and organochlorines (DDT) and the large presence of target site insensitivity. The results demonstrate the need for Rwanda to expand monitoring for insecticide resistance including further metabolic resistance testing and implement an insecticide resistance management strategy to sustain the gains made in malaria control. BioMed Central 2016-12-01 /pmc/articles/PMC5134262/ /pubmed/27905919 http://dx.doi.org/10.1186/s12936-016-1618-6 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
Hakizimana, Emmanuel
Karema, Corine
Munyakanage, Dunia
Iranzi, Gad
Githure, John
Tongren, Jon Eric
Takken, Willem
Binagwaho, Agnes
Koenraadt, Constantianus J. M.
Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title_full Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title_fullStr Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title_full_unstemmed Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title_short Susceptibility of Anopheles gambiae to insecticides used for malaria vector control in Rwanda
title_sort susceptibility of anopheles gambiae to insecticides used for malaria vector control in rwanda
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134262/
https://www.ncbi.nlm.nih.gov/pubmed/27905919
http://dx.doi.org/10.1186/s12936-016-1618-6
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