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Genetic variation at the Cyp6m2 putative insecticide resistance locus in Anopheles gambiae and Anopheles coluzzii

View ORCID ProfileMartin G. Wagah, View ORCID ProfilePetra Korlević, Christopher Clarkson, View ORCID ProfileAlistair Miles, The Anopheles gambiae 1000 Genomes Consortium, View ORCID ProfileMara K. N. Lawniczak, Alex Makunin
doi: https://doi.org/10.1101/2020.11.12.378943
Martin G. Wagah
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
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  • For correspondence: mw21@sanger.ac.uk
Petra Korlević
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
2European Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
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Christopher Clarkson
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
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Alistair Miles
3University of Oxford, Wellcome Trust Centre for Human Genetics, Oxford, OX3 7BN, United Kingdom
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1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
Mara K. N. Lawniczak
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
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Alex Makunin
1Wellcome Sanger Institute, Hinxton, Cambridgeshire, CB10 1SD, United Kingdom
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Abstract

Background The emergence of insecticide resistance is a major threat to malaria control programmes in Africa, with many different factors contributing to insecticide resistance in its vectors, Anopheles mosquitoes. CYP6M2 has previously been recognized as an important candidate in cytochrome P450-mediated detoxification in Anopheles mosquitoes. As it has been implicated in resistance against pyrethroids, organochlorines and carbamates, its broad metabolic activity makes it a potential agent in insecticide cross-resistance. Currently, allelic variation within the Cyp6m2 gene remains unknown.

Results Here, we use Illumina whole-genome sequence data from Phase 2 of the Anopheles gambiae 1000 Genomes Project (Ag1000G) to examine genetic variation in the Cyp6m2 gene across 16 populations in 13 countries comprising Anopheles gambiae and Anopheles coluzzii mosquitoes. We find 15 missense biallelic substitutions at high frequency (defined as >5% frequency in one or more populations), that fall into five distinct haplotype groups that carry the main high frequency variants: A13T, D65A, E328Q, Y347F, I359V and A468S. We examine whether these alleles show evidence of selection either through potentially modified enzymatic function or by being linked to variants that change the transcriptional profile of the gene. Despite consistent reports of Cyp6m2 upregulation and metabolic activity in insecticide resistant Anophelines, we find no evidence of directional selection occurring on these variants or on the haplotype clusters in which they are found.

Conclusion Our results imply that emerging resistance associated with Cyp6m2 is potentially driven by distant regulatory loci such as transcriptional factors rather than by its missense variants, or that other genes are playing a more significant role in conferring metabolic resistance.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://www.malariagen.net/data/ag1000g-phase-2-ar1

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted November 13, 2020.
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Genetic variation at the Cyp6m2 putative insecticide resistance locus in Anopheles gambiae and Anopheles coluzzii
Martin G. Wagah, Petra Korlević, Christopher Clarkson, Alistair Miles, The Anopheles gambiae 1000 Genomes Consortium, Mara K. N. Lawniczak, Alex Makunin
bioRxiv 2020.11.12.378943; doi: https://doi.org/10.1101/2020.11.12.378943
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Genetic variation at the Cyp6m2 putative insecticide resistance locus in Anopheles gambiae and Anopheles coluzzii
Martin G. Wagah, Petra Korlević, Christopher Clarkson, Alistair Miles, The Anopheles gambiae 1000 Genomes Consortium, Mara K. N. Lawniczak, Alex Makunin
bioRxiv 2020.11.12.378943; doi: https://doi.org/10.1101/2020.11.12.378943

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