Yavaşoğlu Sare İlknur, Şimşek Fatih Mehmet
Department of Biology, Faculty of Science and Arts, Aydın Adnan Menderes University, Aydın, Turkey.
J Arthropod Borne Dis. 2021 Dec 31;15(4):405-420. doi: 10.18502/jad.v15i4.10505. eCollection 2021 Dec.
has a significant public health importance since it is an important vector of West Nile virus and Rift Valley fever virus. We, therefore, aimed to determine the insecticide resistance level in populations in the Aegean and Mediterranean regions of Turkey.
Bioassays have been carried out against Dichlorodiphenyltrichloroethane (DDT) (4%), Malathion (5%), Fenitrothion (1%), Propoxur (0.1%), Bendiocarb (0.1%), Permethrin (0.75%) and Deltamethrin (0.05%). Biochemical analyses have been performed to detect non-specific esterase, mixed function oxidase, glutathione-s-transferase and acetylcholinesterase levels. A knockdown resistance ( (L1014F) and Acetylcholinesterase (Ace-1) (G119S) mutations have been detected by using allele-specific primers and a polymerase chain reaction (PCR) amplification of specific alleles (PASA) diagnostic test was performed for detection of F290V mutation.
Bioassay results showed that all populations were resistant to DDT, Malathion, Fenitrothion, Bendiocarb, Propoxur and some of the populations have started to gain Permethrin and Deltamethrin resistance. Biochemical analyses results revealed that altered glutathione-s-transferases, P450 monooxygenases, esterase levels might be responsible for DDT, organophosphate, carbamate and pyrethroid resistance in populations. Results showed mild to high frequency of L1014F, low frequency of F290V but no Ace-1 G119S mutation within the populations. Additionally, acetylcholinesterase insensitivity was not significantly high within the most of these populations.
Overall results may help to fulfil the lacking information in the literature regarding insecticide resistance status and underlying mechanism of populations of the Mediterranean and Aegean region of Turkey by using all bioassays, molecular tests and biochemical assays.
由于它是西尼罗河病毒和裂谷热病毒的重要传播媒介,具有重大的公共卫生意义。因此,我们旨在确定土耳其爱琴海和地中海地区种群的杀虫剂抗性水平。
针对滴滴涕(4%)、马拉硫磷(5%)、杀螟硫磷(1%)、残杀威(0.1%)、恶虫威(0.1%)、氯菊酯(0.75%)和溴氰菊酯(0.05%)进行了生物测定。进行了生化分析以检测非特异性酯酶、混合功能氧化酶、谷胱甘肽 - s - 转移酶和乙酰胆碱酯酶水平。通过使用等位基因特异性引物检测击倒抗性(L1014F)和乙酰胆碱酯酶(Ace - 1)(G119S)突变,并进行了特定等位基因的聚合酶链反应(PCR)扩增(PASA)诊断测试以检测F290V突变。
生物测定结果表明,所有种群对滴滴涕、马拉硫磷、杀螟硫磷、恶虫威、残杀威均有抗性,部分种群已开始对氯菊酯和溴氰菊酯产生抗性。生化分析结果显示,谷胱甘肽 - s - 转移酶、P450单加氧酶、酯酶水平的改变可能是种群对滴滴涕、有机磷、氨基甲酸酯和拟除虫菊酯产生抗性的原因。结果显示种群中L1014F频率为轻度至高频,F290V频率较低,但未检测到Ace - 1 G119S突变。此外,在这些种群中的大多数中,乙酰胆碱酯酶不敏感性并不显著高。
总体结果可能有助于通过使用所有生物测定、分子测试和生化测定来填补文献中关于土耳其地中海和爱琴海地区种群杀虫剂抗性状况及潜在机制的缺失信息。