Tatchou-Nebangwa Nelly M T, Mugenzi Leon M J, Muhammad Abdullahi, Nebangwa Derrick N, Kouamo Mersimine F M, Tagne Carlos S Djoko, Tekoh Theofelix A, Tchouakui Magellan, Ghogomu Stephen M, Ibrahim Sulaiman S, Wondji Charles S
Centre for Research in Infectious Diseases (CRID), P.O. BOX 13591, Yaounde, Cameroon.
Department of Biochemistry and Molecular Biology, Faculty of Science, University of Buea, P.O. Box 63, Buea, Cameroon.
BMC Biol. 2024 Dec 18;22(1):286. doi: 10.1186/s12915-024-02081-y.
Gaining a comprehensive understanding of the genetic mechanisms underlying insecticide resistance in malaria vectors is crucial for optimising the effectiveness of insecticide-based vector control methods and developing diagnostic tools for resistance management. Considering the heterogeneity of metabolic resistance in major malaria vectors, the implementation of tailored resistance management strategies is essential for successful vector control. Here, we provide evidence demonstrating that two highly selected mutations in CYP6P4a and CYP6P4b are driving pyrethroid insecticide resistance in the major malaria vector Anopheles funestus, in West Africa.
Continent-wide polymorphism survey revealed escalated signatures of directional selection of both genes between 2014 and 2021. In vitro insecticide metabolism assays with recombinant enzymes from both genes showed that mutant alleles under selection exhibit higher metabolic efficiency than their wild-type counterparts. Using the GAL4-UAS expression system, transgenic Drosophila flies overexpressing mutant alleles exhibited increased resistance to pyrethroids. These findings were consistent with in silico predictions which highlighted changes in enzyme active site architecture that enhance the affinity of mutant alleles for type I and II pyrethroids. Furthermore, we designed two DNA-based assays for the detection of CYP6P4a-M220I and CYP6P4b-D284E mutations, showing their current confinement to West Africa. Genotype/phenotype correlation analyses revealed that these markers are strongly associated with resistance to types I and II pyrethroids and combine to drastically reduce killing effects of pyrethroid bed nets.
Overall, this study demonstrated that CYP6P4a and CYP6P4b contribute to pyrethroid resistance in An. funestus and provided two additional insecticide resistance molecular diagnostic tools that would contribute to monitoring and better management of resistance.
全面了解疟蚊抗杀虫剂的遗传机制对于优化基于杀虫剂的病媒控制方法的有效性以及开发抗药性管理诊断工具至关重要。考虑到主要疟蚊代谢抗性的异质性,实施针对性的抗性管理策略对于成功控制病媒至关重要。在此,我们提供证据表明,在西非主要疟蚊冈比亚按蚊中,CYP6P4a和CYP6P4b中的两个高度选择的突变正在导致拟除虫菊酯类杀虫剂抗性。
全大陆范围的多态性调查显示,2014年至2021年间这两个基因的定向选择特征有所增加。对来自这两个基因的重组酶进行的体外杀虫剂代谢试验表明,被选择的突变等位基因比其野生型对应物表现出更高的代谢效率。使用GAL4-UAS表达系统,过表达突变等位基因的转基因果蝇对拟除虫菊酯类杀虫剂的抗性增强。这些发现与计算机模拟预测结果一致,该预测突出了酶活性位点结构的变化,这些变化增强了突变等位基因对I型和II型拟除虫菊酯类杀虫剂的亲和力。此外,我们设计了两种基于DNA的检测方法来检测CYP6P4a-M220I和CYP6P4b-D284E突变,结果表明它们目前仅限于西非。基因型/表型相关性分析表明,这些标记与对I型和II型拟除虫菊酯类杀虫剂的抗性密切相关,并且共同作用大幅降低了拟除虫菊酯类蚊帐的杀虫效果。
总体而言,本研究表明CYP6P4a和CYP6P4b促成了冈比亚按蚊对拟除虫菊酯类杀虫剂的抗性,并提供了另外两种杀虫剂抗性分子诊断工具,这将有助于监测和更好地管理抗药性。