bioRxivGeneticsPreprint
Overexpression and nonsynonymous mutations of UDP-glycosyltransferases potentially associated with pyrethroid resistance in Anopheles funestus
Talal Al‐YazeediiD, Abdullahi MuhammadiD, Helen Irving, Seung‐Joon AhniD, Jack HearniD, Charles Sinclair WondjiiD
Abstract
UDP-glycosyltransferases (UGTs) constitute a superfamily of enzymes that play a vital role in the biotransformation of diverse hydrophobic substrates into more hydrophilic products, thereby facilitating their excretion from the cell through transporters. The significance of UGTs in conferring insecticide resistance has been emphasized in various insect species. In this study, we characterised Anopheles funestus UGT genes genome-wide and explored their evolution and association with pyrethroid resistance. We combined genome-wide association of pooled-template sequencing (GWAS-PoolSeq) with the transcriptomic profile of pyrethroid-resistant An. funestus populations, and deep targeted sequencing of UGTs from 80 individual mosquitoes collected in Malawi, Uganda, Cameroon and the two laboratory colonies (FANG and FUMOZ) to investigate the role of UGTs in pyrethroid resistance. We identified common overexpression of UGT310B2 (AFUN000679) in the resistant laboratory colony (FUMOZ) and resistant field populations from Malawi, Cameroon and Uganda. Significant gene-wise Fst differentiation between the resistant and putatively susceptible populations was observed for UGT301C2 and UGT302A3 in Malawi, as well as UGT306C2 in Uganda. Furthermore, the gene-wise Tajimas D density curves of the sequenced regions provided insights into genome-wide processes elucidating population structures within An. funestus populations from these three countries, supporting previous observations. Additionally, we identified significantly differentiated nonsynonymous mutations within UGT genes, which may potentially contribute to pyrethroid resistance. The identified role of An. funestus UGT genes in pyrethroid resistance has direct implications for current vector control strategies, management approaches, and the prediction of potential cross-resistance to other insecticides that can be directly detoxified by UGTs.
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Two highly selected mutations in the tandemly duplicated CYP6P4a and CYP6P4b drive pyrethroid resistance in Anopheles funestus
Nelly M.T. Tatchou-Nebangwa, Leon M. J. Mugenzi, … Charles Sinclair Wondji·bioRxiv·Mar 26, 2024
- A single mutation G454A in P450 CYP9K1 drives pyrethroid resistance in the major malaria vector Anopheles funestus reducing bed net efficacy
Carlos S. D. Tagne, Mersimine Kouamo, … Charles Sinclair Wondji·bioRxiv·Apr 22, 2024
- Multi-omics analysis identifies a CYP9K1 haplotype conferring pyrethroid resistance in the malaria vector Anopheles funestus in East Africa
Jack Hearn, Carlos S. D. Tagne, … Charles Sinclair Wondji·Molecular EcologyPeer-reviewed·May 12, 2022
- Functional genetic validation of key genes conferringinsecticide resistance in the major African malaria vector,Anopheles gambiae
Adriana Adolfi, Beth C. Poulton, … Gareth John Lycett·Proceedings of the National Academy of SciencesPeer-reviewed·Dec 4, 2019
- Genome-wide gene expression profiling reveals that cuticle alterations and P450 detoxification are associated with pyrethroid resistance in Anopheles arabiensis populations from Ethiopia
Eba Alemayehu Simma, Wannes Dermauw, … Thomas Van Leeuwen·Pest Management SciencePeer-reviewed·Feb 11, 2019
- Signatures of selection and mechanisms of insecticide resistance in Ugandan Anopheles funestus: Insights from embedding translational genomics into the LLINEUP cluster randomised trial.
Lilian Namuli-Kayondo, Sanjay Curtis Nagi, … Martin J. Donnelly·bioRxiv·Jun 17, 2025