Susceptibility to organophosphate insecticides in Aedes aegypti (Diptera: Culicidae) from northern Colombia and associated resistance mechanisms.

IF 3 2区 医学 Q1 PARASITOLOGY Parasites & Vectors Pub Date : 2025-01-14 DOI:10.1186/s13071-024-06624-8
María Claudia Atencia-Pineda, Javier García-Leal, Diana Diaz-Ortiz, Paula Pareja-Loaiza, Lisandro Pacheco-Lugo, Richard Hoyos-López, Alfonso Calderón-Rangel, Pedro Fragozo-Castilla, Selene M Gutiérrez-Rodríguez, Adriana E Flores, Ronald Maestre-Serrano
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引用次数: 0

Abstract

Background: Aedes aegypti is the primary vector of dengue, chikungunya, and Zika viruses in Colombia. Various insecticides, including pyrethroid, organophosphate, and carbamate insecticides; growth regulators; and biological insecticides, such as Bacillus thuringiensis var. israelensis, have been used to control Ae. aegypti populations. However, organophosphates such as malathion, pirimiphos-methyl, and temephos have been used over the last decade owing to the high resistance to pyrethroids.

Methods: This study assessed the susceptibility to organophosphates in 14 Ae. aegypti populations from the Córdoba department in northern Colombia. Moreover, possible resistance mechanisms were investigated by determining the activity levels of α-esterases, β-esterases, mixed function oxidases (MFOs), glutathione S-transferases (GSTs), and insensitive acetylcholinesterase (iAChE). Additionally, the Ace-1 gene was sequenced to identify mutations at the target site of action.

Results: The populations were susceptible to temephos and malathion but resistant to fenitrothion, and in three of them, to pirimiphos-methyl. Alterations in the enzyme activity levels of α-esterases and β-esterases, GST, and iAChE were observed among the populations, with high enzyme activity levels of α and β esterases associated with resistance to fenitrothion. No mutations were identified in the Ace-1 gene.

Conclusions: These findings are highly relevant for vector control programs in the region, as they allow for adjustments in resistance management strategies and improve the effectiveness of interventions against these arboviruses.

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背景:埃及伊蚊是哥伦比亚登革热、基孔肯雅和寨卡病毒的主要传播媒介。各种杀虫剂,包括拟除虫菊酯类、有机磷类和氨基甲酸酯类杀虫剂;生长调节剂;以及生物杀虫剂,如苏云金芽孢杆菌(Bacillus thuringiensis var. israelensis),已被用于控制埃及伊蚊的数量。然而,由于对拟除虫菊酯的抗药性很强,过去十年中一直在使用马拉硫磷、甲基吡啶磷和特灭磷等有机磷杀虫剂:本研究评估了哥伦比亚北部科尔多瓦省 14 个埃及蝇种群对有机磷的敏感性。此外,通过测定α-酯酶、β-酯酶、混合功能氧化酶(MFO)、谷胱甘肽 S-转移酶(GST)和不敏感乙酰胆碱酯酶(iAChE)的活性水平,研究了可能的抗性机制。此外,还对 Ace-1 基因进行了测序,以确定目标作用位点的突变:结果:这些种群对特灭磷和马拉硫磷易感,但对杀螟硫磷有抗性,其中三个种群对甲基吡啶磷有抗性。在不同种群中观察到了α酯酶和β酯酶、GST和iAChE酶活性水平的变化,其中α和β酯酶的高酶活性水平与对杀螟硫磷的抗性有关。在 Ace-1 基因中未发现突变:这些发现与该地区的病媒控制计划密切相关,因为它们有助于调整抗药性管理策略,提高对这些虫媒病毒的干预效果。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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