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A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae

The spread of resistance to insecticides in disease-carrying mosquitoes poses a threat to the effectiveness of control programmes, which rely largely on insecticide-based interventions. Monitoring mosquito populations is essential, but obtaining phenotypic measurements of resistance is laborious and...

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Autores principales: Lucas, Eric R., Rockett, Kirk A., Lynd, Amy, Essandoh, John, Grisales, Nelson, Kemei, Brigid, Njoroge, Harun, Hubbart, Christina, Rippon, Emily J., Morgan, John, Van’t Hof, Arjen E., Ochomo, Eric O., Kwiatkowski, Dominic P., Weetman, David, Donnelly, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746726/
https://www.ncbi.nlm.nih.gov/pubmed/31527637
http://dx.doi.org/10.1038/s41598-019-49892-6
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author Lucas, Eric R.
Rockett, Kirk A.
Lynd, Amy
Essandoh, John
Grisales, Nelson
Kemei, Brigid
Njoroge, Harun
Hubbart, Christina
Rippon, Emily J.
Morgan, John
Van’t Hof, Arjen E.
Ochomo, Eric O.
Kwiatkowski, Dominic P.
Weetman, David
Donnelly, Martin J.
author_facet Lucas, Eric R.
Rockett, Kirk A.
Lynd, Amy
Essandoh, John
Grisales, Nelson
Kemei, Brigid
Njoroge, Harun
Hubbart, Christina
Rippon, Emily J.
Morgan, John
Van’t Hof, Arjen E.
Ochomo, Eric O.
Kwiatkowski, Dominic P.
Weetman, David
Donnelly, Martin J.
author_sort Lucas, Eric R.
collection PubMed
description The spread of resistance to insecticides in disease-carrying mosquitoes poses a threat to the effectiveness of control programmes, which rely largely on insecticide-based interventions. Monitoring mosquito populations is essential, but obtaining phenotypic measurements of resistance is laborious and error-prone. High-throughput genotyping offers the prospect of quick and repeatable estimates of resistance, while also allowing resistance markers to be tracked and studied. To demonstrate the potential of highly-mulitplexed genotypic screening for measuring resistance-association of mutations and tracking their spread, we developed a panel of 28 known or putative resistance markers in the major malaria vector Anopheles gambiae, which we used to screen mosquitoes from a wide swathe of Sub-Saharan Africa (Burkina Faso, Ghana, Democratic Republic of Congo (DRC) and Kenya). We found resistance association in four markers, including a novel mutation in the detoxification gene Gste2 (Gste2-119V). We also identified a duplication in Gste2 combining a resistance-associated mutation with its wild-type counterpart, potentially alleviating the costs of resistance. Finally, we describe the distribution of the multiple origins of kdr resistance, finding unprecedented diversity in the DRC. This panel represents the first step towards a quantitative genotypic model of insecticide resistance that can be used to predict resistance status in An. gambiae.
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spelling pubmed-67467262019-09-27 A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae Lucas, Eric R. Rockett, Kirk A. Lynd, Amy Essandoh, John Grisales, Nelson Kemei, Brigid Njoroge, Harun Hubbart, Christina Rippon, Emily J. Morgan, John Van’t Hof, Arjen E. Ochomo, Eric O. Kwiatkowski, Dominic P. Weetman, David Donnelly, Martin J. Sci Rep Article The spread of resistance to insecticides in disease-carrying mosquitoes poses a threat to the effectiveness of control programmes, which rely largely on insecticide-based interventions. Monitoring mosquito populations is essential, but obtaining phenotypic measurements of resistance is laborious and error-prone. High-throughput genotyping offers the prospect of quick and repeatable estimates of resistance, while also allowing resistance markers to be tracked and studied. To demonstrate the potential of highly-mulitplexed genotypic screening for measuring resistance-association of mutations and tracking their spread, we developed a panel of 28 known or putative resistance markers in the major malaria vector Anopheles gambiae, which we used to screen mosquitoes from a wide swathe of Sub-Saharan Africa (Burkina Faso, Ghana, Democratic Republic of Congo (DRC) and Kenya). We found resistance association in four markers, including a novel mutation in the detoxification gene Gste2 (Gste2-119V). We also identified a duplication in Gste2 combining a resistance-associated mutation with its wild-type counterpart, potentially alleviating the costs of resistance. Finally, we describe the distribution of the multiple origins of kdr resistance, finding unprecedented diversity in the DRC. This panel represents the first step towards a quantitative genotypic model of insecticide resistance that can be used to predict resistance status in An. gambiae. Nature Publishing Group UK 2019-09-16 /pmc/articles/PMC6746726/ /pubmed/31527637 http://dx.doi.org/10.1038/s41598-019-49892-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lucas, Eric R.
Rockett, Kirk A.
Lynd, Amy
Essandoh, John
Grisales, Nelson
Kemei, Brigid
Njoroge, Harun
Hubbart, Christina
Rippon, Emily J.
Morgan, John
Van’t Hof, Arjen E.
Ochomo, Eric O.
Kwiatkowski, Dominic P.
Weetman, David
Donnelly, Martin J.
A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title_full A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title_fullStr A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title_full_unstemmed A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title_short A high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in Anopheles gambiae
title_sort high throughput multi-locus insecticide resistance marker panel for tracking resistance emergence and spread in anopheles gambiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746726/
https://www.ncbi.nlm.nih.gov/pubmed/31527637
http://dx.doi.org/10.1038/s41598-019-49892-6
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