在连续复制的CYP6P4a和CYP6P4b基因中,两个高度选择的突变驱动了西非funestus按蚊对拟除虫菊酯的抗性。

IF 4.4 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2024-12-18 DOI:10.1186/s12915-024-02081-y
Nelly M T Tatchou-Nebangwa, Leon M J Mugenzi, Abdullahi Muhammad, Derrick N Nebangwa, Mersimine F M Kouamo, Carlos S Djoko Tagne, Theofelix A Tekoh, Magellan Tchouakui, Stephen M Ghogomu, Sulaiman S Ibrahim, Charles S Wondji
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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.</p><p><strong>Results: </strong>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. 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引用次数: 0

摘要

背景:全面了解疟疾病媒对杀虫剂耐药性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和开发耐药性管理的诊断工具至关重要。考虑到主要疟疾病媒代谢耐药性的异质性,实施有针对性的耐药性管理战略对于成功控制病媒至关重要。在这里,我们提供的证据表明,CYP6P4a和CYP6P4b两个高度选择的突变驱动了西非主要疟疾媒介按蚊(Anopheles funestus)对拟除虫菊酯杀虫剂的抗性。结果:全大陆多态性调查显示,2014年至2021年间,这两个基因的定向选择特征不断升级。用这两个基因的重组酶进行的体外杀虫剂代谢试验表明,选择突变等位基因的代谢效率高于野生型等位基因。利用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的抗性增强。这些发现与计算机预测一致,该预测强调了酶活性位点结构的变化,增强了突变等位基因对I型和II型拟除虫菊酯的亲和力。此外,我们设计了两种基于dna的检测CYP6P4a-M220I和CYP6P4b-D284E突变的方法,显示它们目前仅限于西非。基因型/表型相关分析显示,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,并显著降低了拟除虫菊酯类杀虫剂蚊帐的杀灭效果。结论:总体而言,本研究表明CYP6P4a和CYP6P4b与拟除虫菊酯类杀虫剂抗性有关。Funestus和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性。
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Two highly selected mutations in the tandemly duplicated CYP6P4a and CYP6P4b genes drive pyrethroid resistance in Anopheles funestus in West Africa.

Background: 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.

Results: 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.

Conclusions: 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.

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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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