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Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya

BACKGROUND: Outdoor malaria transmission is becoming an increasingly important problem in malaria control in Africa. Larval control is a promising intervention as it can target both indoor and outdoor biting mosquitoes. However, the currently available biolarvicide formulations have a short effectiv...

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Autores principales: Afrane, Yaw A., Mweresa, Nixon G., Wanjala, Christine L., Gilbreath III, Thomas M., Zhou, Guofa, Lee, Ming-Chieh, Githeko, Andrew K., Yan, Guiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131428/
https://www.ncbi.nlm.nih.gov/pubmed/27903292
http://dx.doi.org/10.1186/s12936-016-1626-6
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author Afrane, Yaw A.
Mweresa, Nixon G.
Wanjala, Christine L.
Gilbreath III, Thomas M.
Zhou, Guofa
Lee, Ming-Chieh
Githeko, Andrew K.
Yan, Guiyun
author_facet Afrane, Yaw A.
Mweresa, Nixon G.
Wanjala, Christine L.
Gilbreath III, Thomas M.
Zhou, Guofa
Lee, Ming-Chieh
Githeko, Andrew K.
Yan, Guiyun
author_sort Afrane, Yaw A.
collection PubMed
description BACKGROUND: Outdoor malaria transmission is becoming an increasingly important problem in malaria control in Africa. Larval control is a promising intervention as it can target both indoor and outdoor biting mosquitoes. However, the currently available biolarvicide formulations have a short effective duration, and consequently larval control incurs a high operational expense due to the requirement for frequent re-treatment of larval habitats. Formulations of biolarvicides with long-lasting effects is highly desired. A recently developed FourStar® slow-release briquet formulation of Bacillus thuringiensis israelensis and Bacillus sphaericus was evaluated to test its efficacy on malaria vectors. METHODS: The study evaluated FourStar™ briquets 180-days formulation under semi-natural and natural conditions to test their efficacy in reducing the mosquito population in western Kenya. The semi-natural habitats used the formulation dissolved in rainwater with appropriate concentrations, and second-instar larvae of Anopheles gambiae were introduced and the number of surviving larvae and pupae produced was recorded daily as the outcome. The briquets formulation was then tested in natural habitats for efficacy on pupal productivity reduction in highland and lowland sites in western Kenya. The formulation was finally tested for efficacy in reducing adult mosquito populations in randomized clusters in western Kenya highland. RESULTS: In semi-natural conditions, the FourStar™ briquets 180-days formulation completely inhibited mosquito pupal production in the first 3 months, and then reduced pupal productivity by 87–98% (P < 0.001) 4–6 months after application. In natural habitats, during the first 2 months no pupae were detected from any of the treated habitats in highland sites, and Anopheles spp. pupal density was reduced by 60–90% in the next 3–5 months (P < 0.001). In the lowland site, pupal productivity reduction was 100% in the first 3 months, and 75–90% in the next 4–5 months (P < 0.001). The randomized cluster trial found that the application of the briquets formulation reduced mean densities of indoor-biting mosquitoes by 76–82% (P < 0.001) and by 67–75% (P < 0.001) for outdoor-biting mosquitoes. CONCLUSION: This study demonstrated that long-lasting biological larviciding was effective in reducing pupal productivity of larval habitats, and reducing indoor and outdoor resting mosquitoes. The study suggests that long-lasting microbial larviciding may be a promising complementary malaria vector control tool and warrants further large-scale evaluation.
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spelling pubmed-51314282016-12-12 Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya Afrane, Yaw A. Mweresa, Nixon G. Wanjala, Christine L. Gilbreath III, Thomas M. Zhou, Guofa Lee, Ming-Chieh Githeko, Andrew K. Yan, Guiyun Malar J Research BACKGROUND: Outdoor malaria transmission is becoming an increasingly important problem in malaria control in Africa. Larval control is a promising intervention as it can target both indoor and outdoor biting mosquitoes. However, the currently available biolarvicide formulations have a short effective duration, and consequently larval control incurs a high operational expense due to the requirement for frequent re-treatment of larval habitats. Formulations of biolarvicides with long-lasting effects is highly desired. A recently developed FourStar® slow-release briquet formulation of Bacillus thuringiensis israelensis and Bacillus sphaericus was evaluated to test its efficacy on malaria vectors. METHODS: The study evaluated FourStar™ briquets 180-days formulation under semi-natural and natural conditions to test their efficacy in reducing the mosquito population in western Kenya. The semi-natural habitats used the formulation dissolved in rainwater with appropriate concentrations, and second-instar larvae of Anopheles gambiae were introduced and the number of surviving larvae and pupae produced was recorded daily as the outcome. The briquets formulation was then tested in natural habitats for efficacy on pupal productivity reduction in highland and lowland sites in western Kenya. The formulation was finally tested for efficacy in reducing adult mosquito populations in randomized clusters in western Kenya highland. RESULTS: In semi-natural conditions, the FourStar™ briquets 180-days formulation completely inhibited mosquito pupal production in the first 3 months, and then reduced pupal productivity by 87–98% (P < 0.001) 4–6 months after application. In natural habitats, during the first 2 months no pupae were detected from any of the treated habitats in highland sites, and Anopheles spp. pupal density was reduced by 60–90% in the next 3–5 months (P < 0.001). In the lowland site, pupal productivity reduction was 100% in the first 3 months, and 75–90% in the next 4–5 months (P < 0.001). The randomized cluster trial found that the application of the briquets formulation reduced mean densities of indoor-biting mosquitoes by 76–82% (P < 0.001) and by 67–75% (P < 0.001) for outdoor-biting mosquitoes. CONCLUSION: This study demonstrated that long-lasting biological larviciding was effective in reducing pupal productivity of larval habitats, and reducing indoor and outdoor resting mosquitoes. The study suggests that long-lasting microbial larviciding may be a promising complementary malaria vector control tool and warrants further large-scale evaluation. BioMed Central 2016-12-01 /pmc/articles/PMC5131428/ /pubmed/27903292 http://dx.doi.org/10.1186/s12936-016-1626-6 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
Afrane, Yaw A.
Mweresa, Nixon G.
Wanjala, Christine L.
Gilbreath III, Thomas M.
Zhou, Guofa
Lee, Ming-Chieh
Githeko, Andrew K.
Yan, Guiyun
Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title_full Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title_fullStr Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title_full_unstemmed Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title_short Evaluation of long-lasting microbial larvicide for malaria vector control in Kenya
title_sort evaluation of long-lasting microbial larvicide for malaria vector control in kenya
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131428/
https://www.ncbi.nlm.nih.gov/pubmed/27903292
http://dx.doi.org/10.1186/s12936-016-1626-6
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