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Characterisation of Anopheles strains used for laboratory screening of new vector control products

BACKGROUND: Insecticides formulated into products that target Anopheles mosquitos have had an immense impact on reducing malaria cases in Africa. However, resistance to currently used insecticides is spreading rapidly and there is an urgent need for alternative public health insecticides. Potential...

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Autores principales: Williams, Jessica, Flood, Lori, Praulins, Giorgio, Ingham, Victoria A., Morgan, John, Lees, Rosemary Susan, Ranson, Hilary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833243/
https://www.ncbi.nlm.nih.gov/pubmed/31690332
http://dx.doi.org/10.1186/s13071-019-3774-3
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author Williams, Jessica
Flood, Lori
Praulins, Giorgio
Ingham, Victoria A.
Morgan, John
Lees, Rosemary Susan
Ranson, Hilary
author_facet Williams, Jessica
Flood, Lori
Praulins, Giorgio
Ingham, Victoria A.
Morgan, John
Lees, Rosemary Susan
Ranson, Hilary
author_sort Williams, Jessica
collection PubMed
description BACKGROUND: Insecticides formulated into products that target Anopheles mosquitos have had an immense impact on reducing malaria cases in Africa. However, resistance to currently used insecticides is spreading rapidly and there is an urgent need for alternative public health insecticides. Potential new insecticides must be screened against a range of characterized mosquito strains to identify potential resistance liabilities. The Liverpool School of Tropical Medicine maintains three susceptible and four resistant Anopheles strains that are widely used for screening for new insecticides. The properties of these strains are described in this paper. METHODS: WHO tube susceptibility bioassays were used for colony selection and to screen for resistance to the major classes of public health insecticides. Topical and tarsal contact bioassays were used to produce dose response curves to assess resistance intensity. Bioassays with the synergist piperonyl butoxide were also performed. Taqman™ assays were used to screen for known target site resistance alleles (kdr and ace-1). RT-qPCR was used to quantify expression of genes associated with pyrethroid resistance. RESULTS: Pyrethroid selection pressure has maintained resistance to this class in all four resistant strains. Some carbamate and organophosphate resistance has been lost through lack of exposure to these insecticide classes. The Anopheles gambiae (sensu lato) strains, VK7 2014, Banfora M and Tiassalé 13 have higher levels of pyrethroid resistance than the An. funestus FUMOZ-R strain. Elevated expression of P450s is found in all four strains and the 1014F kdr mutation is present in all three An. gambiae strains at varying frequencies. Tarsal contact data and overexpression of CYP4G16 and SAP2 suggest penetration barriers and/or sequestration also confer resistance in Banfora M. CONCLUSIONS: Continual selection with deltamethrin has maintained a stable pyrethroid-resistant phenotype over many generations. In conjunction with a standardized rearing regime, this ensures quality control of strains over time allowing for robust product comparison and selection of optimal products for further development. The identification of multiple mechanisms underpinning insecticide resistance highlights the importance of screening new compounds against a range of mosquito strains. [Image: see text]
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spelling pubmed-68332432019-11-08 Characterisation of Anopheles strains used for laboratory screening of new vector control products Williams, Jessica Flood, Lori Praulins, Giorgio Ingham, Victoria A. Morgan, John Lees, Rosemary Susan Ranson, Hilary Parasit Vectors Research BACKGROUND: Insecticides formulated into products that target Anopheles mosquitos have had an immense impact on reducing malaria cases in Africa. However, resistance to currently used insecticides is spreading rapidly and there is an urgent need for alternative public health insecticides. Potential new insecticides must be screened against a range of characterized mosquito strains to identify potential resistance liabilities. The Liverpool School of Tropical Medicine maintains three susceptible and four resistant Anopheles strains that are widely used for screening for new insecticides. The properties of these strains are described in this paper. METHODS: WHO tube susceptibility bioassays were used for colony selection and to screen for resistance to the major classes of public health insecticides. Topical and tarsal contact bioassays were used to produce dose response curves to assess resistance intensity. Bioassays with the synergist piperonyl butoxide were also performed. Taqman™ assays were used to screen for known target site resistance alleles (kdr and ace-1). RT-qPCR was used to quantify expression of genes associated with pyrethroid resistance. RESULTS: Pyrethroid selection pressure has maintained resistance to this class in all four resistant strains. Some carbamate and organophosphate resistance has been lost through lack of exposure to these insecticide classes. The Anopheles gambiae (sensu lato) strains, VK7 2014, Banfora M and Tiassalé 13 have higher levels of pyrethroid resistance than the An. funestus FUMOZ-R strain. Elevated expression of P450s is found in all four strains and the 1014F kdr mutation is present in all three An. gambiae strains at varying frequencies. Tarsal contact data and overexpression of CYP4G16 and SAP2 suggest penetration barriers and/or sequestration also confer resistance in Banfora M. CONCLUSIONS: Continual selection with deltamethrin has maintained a stable pyrethroid-resistant phenotype over many generations. In conjunction with a standardized rearing regime, this ensures quality control of strains over time allowing for robust product comparison and selection of optimal products for further development. The identification of multiple mechanisms underpinning insecticide resistance highlights the importance of screening new compounds against a range of mosquito strains. [Image: see text] BioMed Central 2019-11-05 /pmc/articles/PMC6833243/ /pubmed/31690332 http://dx.doi.org/10.1186/s13071-019-3774-3 Text en © The Author(s) 2019 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
Williams, Jessica
Flood, Lori
Praulins, Giorgio
Ingham, Victoria A.
Morgan, John
Lees, Rosemary Susan
Ranson, Hilary
Characterisation of Anopheles strains used for laboratory screening of new vector control products
title Characterisation of Anopheles strains used for laboratory screening of new vector control products
title_full Characterisation of Anopheles strains used for laboratory screening of new vector control products
title_fullStr Characterisation of Anopheles strains used for laboratory screening of new vector control products
title_full_unstemmed Characterisation of Anopheles strains used for laboratory screening of new vector control products
title_short Characterisation of Anopheles strains used for laboratory screening of new vector control products
title_sort characterisation of anopheles strains used for laboratory screening of new vector control products
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833243/
https://www.ncbi.nlm.nih.gov/pubmed/31690332
http://dx.doi.org/10.1186/s13071-019-3774-3
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