Exploring the molecular mechanisms of increased intensity of pyrethroid resistance in Central African population of a major malaria vector Anopheles coluzzii

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Amen N. Fadel, Sulaiman S. Ibrahim, Maurice M. Sandeu, Claudine Grâce Maffo Tatsinkou, Benjamin D. Menze, Helen Irving, Jack Hearn, Sanjay C. Nagi, Gareth D. Weedall, Ebai Terence, Williams Tchapga, Samuel Wanji, Charles S. Wondji
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Abstract

Molecular mechanisms driving the escalation of pyrethroid resistance in the major malaria mosquitoes of Central Africa remain largely uncharacterized, hindering effective management strategies. Here, resistance intensity and the molecular mechanisms driving it were investigated in a population of Anopheles coluzzii from northern Cameroon. High levels of pyrethroid and organochloride resistance were observed in An. coluzzii population, with no mortality for 1× permethrin; only 11% and 33% mortalities for 5× and 10× permethrin diagnostic concentrations, and <2% mortalities for deltamethrin and DDT, respectively. Moderate bendiocarb resistance (88% mortality) and full susceptibility to malathion were observed. Synergist bioassays with piperonyl butoxide recovered permethrin susceptibility, with mortalities increasing to 53.39%, and 87.30% for 5× and 10× permethrin, respectively, implicating P450 monooxygenases. Synergist bioassays with diethyl maleate (DEM) recovered permethrin and DDT susceptibilities (mortalities increasing to 34.75% and 14.88%, respectively), implicating glutathione S-transferases. RNA-seq-based genome-wide transcriptional analyses supported by quantitative PCR identified glutathione S-transferase, GSTe2 (RNA-seqFC = 2.93 and qRT-PCRFC = 8.4, p < 0.0043) and CYP450, CYP6Z2 (RNA-seqFC = 2.39 and qRT-PCRFC = 11.7, p < 0.0177) as the most overexpressed detoxification genes in the pyrethroid-resistant mosquitoes, compared to mosquitoes of the susceptible Ngousso colony. Other overexpressed genes include P450s, CYP6M2 (FC = 1.68, p < 0.0114), CYP4G16 (FC = 2.02, p < 0.0005), and CYP4G17 (FC = 1.86, p < 0.0276). While high frequency of the 1014F kdr mutation (50%) and low frequencies of 1014S (6.61%) and 1575Y (10.29%) were observed, no ace-1 mutation was detected in bendiocarb-resistant populations, suggesting the preeminent role of metabolic mechanism. Overexpression of metabolic resistance genes (including GSTe2 and CYP6Z2 known to confer resistance to multiple insecticides) in An. coluzzii from the Sudan Savannah of Cameroon highlights the need for alternative management strategies to reduce malaria burden in northern Cameroon.

Abstract Image

探索中非主要疟疾病媒疟原虫对拟除虫菊酯抗药性增强的分子机制
中非主要疟疾蚊虫对拟除虫菊酯抗性升级的分子机制在很大程度上仍未定性,这阻碍了有效的管理策略。本文研究了喀麦隆北部一个 coluzzii 按蚊种群的抗药性强度及其分子机制。coluzzii 对拟除虫菊酯和有机氯的抗药性水平很高,1×氯菊酯无致死率,5×和10×氯菊酯诊断浓度的致死率分别为11%和33%,溴氰菊酯和滴滴涕的致死率分别为<2%。观察到对苯敌威有中度抗药性(88% 的死亡率),对马拉硫磷则完全敏感。与胡椒基丁醚的增效生物测定恢复了对氯菊酯的敏感性,5 倍和 10 倍氯菊酯的死亡率分别增加到 53.39% 和 87.30%,这与 P450 单氧化酶有关。马来酸二乙酯(DEM)的增效生物测定恢复了对氯菊酯和滴滴涕的敏感性(死亡率分别增加到 34.75% 和 14.88%),这与谷胱甘肽 S 转移酶有关。定量 PCR 支持的基于 RNA-seq 的全基因组转录分析确定了谷胱甘肽 S-转移酶 GSTe2(RNA-seqFC = 2.93 和 qRT-PCRFC = 8.4,p < 0.0043)和 CYP450、CYP6Z2(RNA-seqFC = 2.39 和 qRT-PCRFC = 11.7, p < 0.0177)是与易受影响的 Ngousso 蚊群相比,抗拟除虫菊酯蚊子中表达量最高的解毒基因。其他高表达基因包括 P450s、CYP6M2(FC = 1.68,p < 0.0114)、CYP4G16(FC = 2.02,p < 0.0005)和 CYP4G17(FC = 1.86,p < 0.0276)。虽然 1014F kdr 突变的频率较高(50%),1014S(6.61%)和 1575Y(10.29%)的频率较低,但在苯替卡因耐药人群中未检测到 ace-1 突变,这表明代谢机制起着重要作用。在喀麦隆苏丹大草原的 An. coluzzii 中,新陈代谢抗性基因(包括 GSTe2 和 CYP6Z2,已知可赋予其对多种杀虫剂的抗性)的过度表达突出表明,有必要采取替代管理策略,以减轻喀麦隆北部的疟疾负担。
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来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
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