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Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment

Studies of insecticide resistance provide insights into the capacity of populations to show rapid evolutionary responses to contemporary selection. Malaria control remains heavily dependent on pyrethroid insecticides, primarily in long lasting insecticidal nets (LLINs). Resistance in the major malar...

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Autores principales: Njoroge, Harun, van't Hof, Arjen, Oruni, Ambrose, Pipini, Dimitra, Nagi, Sanjay C., Lynd, Amy, Lucas, Eric R., Tomlinson, Sean, Grau‐Bove, Xavi, McDermott, Daniel, Wat'senga, Francis T., Manzambi, Emile Z., Agossa, Fiacre R., Mokuba, Arlette, Irish, Seth, Kabula, Bilali, Mbogo, Charles, Bargul, Joel, Paine, Mark J. I., Weetman, David, Donnelly, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424592/
https://www.ncbi.nlm.nih.gov/pubmed/35775282
http://dx.doi.org/10.1111/mec.16591
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author Njoroge, Harun
van't Hof, Arjen
Oruni, Ambrose
Pipini, Dimitra
Nagi, Sanjay C.
Lynd, Amy
Lucas, Eric R.
Tomlinson, Sean
Grau‐Bove, Xavi
McDermott, Daniel
Wat'senga, Francis T.
Manzambi, Emile Z.
Agossa, Fiacre R.
Mokuba, Arlette
Irish, Seth
Kabula, Bilali
Mbogo, Charles
Bargul, Joel
Paine, Mark J. I.
Weetman, David
Donnelly, Martin J.
author_facet Njoroge, Harun
van't Hof, Arjen
Oruni, Ambrose
Pipini, Dimitra
Nagi, Sanjay C.
Lynd, Amy
Lucas, Eric R.
Tomlinson, Sean
Grau‐Bove, Xavi
McDermott, Daniel
Wat'senga, Francis T.
Manzambi, Emile Z.
Agossa, Fiacre R.
Mokuba, Arlette
Irish, Seth
Kabula, Bilali
Mbogo, Charles
Bargul, Joel
Paine, Mark J. I.
Weetman, David
Donnelly, Martin J.
author_sort Njoroge, Harun
collection PubMed
description Studies of insecticide resistance provide insights into the capacity of populations to show rapid evolutionary responses to contemporary selection. Malaria control remains heavily dependent on pyrethroid insecticides, primarily in long lasting insecticidal nets (LLINs). Resistance in the major malaria vectors has increased in concert with the expansion of LLIN distributions. Identifying genetic mechanisms underlying high‐level resistance is crucial for the development and deployment of resistance‐breaking tools. Using the Anopheles gambiae 1000 genomes (Ag1000g) data we identified a very recent selective sweep in mosquitoes from Uganda which localized to a cluster of cytochrome P450 genes. Further interrogation revealed a haplotype involving a trio of mutations, a nonsynonymous point mutation in Cyp6p4 (I236M), an upstream insertion of a partial Zanzibar‐like transposable element (TE) and a duplication of the Cyp6aa1 gene. The mutations appear to have originated recently in An. gambiae from the Kenya‐Uganda border, with stepwise replacement of the double‐mutant (Zanzibar‐like TE and Cyp6p4‐236 M) with the triple‐mutant haplotype (including Cyp6aa1 duplication), which has spread into the Democratic Republic of Congo and Tanzania. The triple‐mutant haplotype is strongly associated with increased expression of genes able to metabolize pyrethroids and is strongly predictive of resistance to pyrethroids most notably deltamethrin. Importantly, there was increased mortality in mosquitoes carrying the triple‐mutation when exposed to nets cotreated with the synergist piperonyl butoxide (PBO). Frequencies of the triple‐mutant haplotype remain spatially variable within countries, suggesting an effective marker system to guide deployment decisions for limited supplies of PBO‐pyrethroid cotreated LLINs across African countries.
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spelling pubmed-94245922022-08-30 Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment Njoroge, Harun van't Hof, Arjen Oruni, Ambrose Pipini, Dimitra Nagi, Sanjay C. Lynd, Amy Lucas, Eric R. Tomlinson, Sean Grau‐Bove, Xavi McDermott, Daniel Wat'senga, Francis T. Manzambi, Emile Z. Agossa, Fiacre R. Mokuba, Arlette Irish, Seth Kabula, Bilali Mbogo, Charles Bargul, Joel Paine, Mark J. I. Weetman, David Donnelly, Martin J. Mol Ecol ORIGINAL ARTICLES Studies of insecticide resistance provide insights into the capacity of populations to show rapid evolutionary responses to contemporary selection. Malaria control remains heavily dependent on pyrethroid insecticides, primarily in long lasting insecticidal nets (LLINs). Resistance in the major malaria vectors has increased in concert with the expansion of LLIN distributions. Identifying genetic mechanisms underlying high‐level resistance is crucial for the development and deployment of resistance‐breaking tools. Using the Anopheles gambiae 1000 genomes (Ag1000g) data we identified a very recent selective sweep in mosquitoes from Uganda which localized to a cluster of cytochrome P450 genes. Further interrogation revealed a haplotype involving a trio of mutations, a nonsynonymous point mutation in Cyp6p4 (I236M), an upstream insertion of a partial Zanzibar‐like transposable element (TE) and a duplication of the Cyp6aa1 gene. The mutations appear to have originated recently in An. gambiae from the Kenya‐Uganda border, with stepwise replacement of the double‐mutant (Zanzibar‐like TE and Cyp6p4‐236 M) with the triple‐mutant haplotype (including Cyp6aa1 duplication), which has spread into the Democratic Republic of Congo and Tanzania. The triple‐mutant haplotype is strongly associated with increased expression of genes able to metabolize pyrethroids and is strongly predictive of resistance to pyrethroids most notably deltamethrin. Importantly, there was increased mortality in mosquitoes carrying the triple‐mutation when exposed to nets cotreated with the synergist piperonyl butoxide (PBO). Frequencies of the triple‐mutant haplotype remain spatially variable within countries, suggesting an effective marker system to guide deployment decisions for limited supplies of PBO‐pyrethroid cotreated LLINs across African countries. John Wiley and Sons Inc. 2022-07-12 2022-08 /pmc/articles/PMC9424592/ /pubmed/35775282 http://dx.doi.org/10.1111/mec.16591 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle ORIGINAL ARTICLES
Njoroge, Harun
van't Hof, Arjen
Oruni, Ambrose
Pipini, Dimitra
Nagi, Sanjay C.
Lynd, Amy
Lucas, Eric R.
Tomlinson, Sean
Grau‐Bove, Xavi
McDermott, Daniel
Wat'senga, Francis T.
Manzambi, Emile Z.
Agossa, Fiacre R.
Mokuba, Arlette
Irish, Seth
Kabula, Bilali
Mbogo, Charles
Bargul, Joel
Paine, Mark J. I.
Weetman, David
Donnelly, Martin J.
Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title_full Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title_fullStr Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title_full_unstemmed Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title_short Identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in Anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
title_sort identification of a rapidly‐spreading triple mutant for high‐level metabolic insecticide resistance in anopheles gambiae provides a real‐time molecular diagnostic for antimalarial intervention deployment
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424592/
https://www.ncbi.nlm.nih.gov/pubmed/35775282
http://dx.doi.org/10.1111/mec.16591
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