Wanjala Christine Ludwin, Kweka Eliningaya J
Department of Medical Laboratory Sciences, Masinde Muliro University of Science and Technology, Kakamega, Kenya.
Department of Zoological Sciences, Kenyatta University, Nairobi, Kenya.
Front Public Health. 2018 Mar 1;6:55. doi: 10.3389/fpubh.2018.00055. eCollection 2018.
Malaria vector control efforts have taken malaria related cases down to appreciable number per annum after large scale of intervention tools. Insecticides-based tools remain the major control option for malaria vectors in Kenya and, therefore, the potential of such programs to be compromised by the reported insecticide resistance is of major concern. The objective of this study was to evaluate the status of insecticide resistance in malaria vectors in different agro ecosystems from western Kenya.
The study was carried out in the lowlands and highlands of western Kenya namely; Ahero, Kisian, Chulaimbo, Emutete, Emakakha, Iguhu, and Kabula. World Health Organization tube bioassays was conducted using standard diagnostic dosages of Lambdacyhalothrin, Deltamethrin, Permethrin, DDT, Bendiocarb, and Malathion tested on mosquitoes collected from seven sites; Ahero, Kisian, Chulaimbo, Emutete, Emakakha, Iguhu, and Kabula. Biochemical assays, where the enzymatic activity of three enzymes (monooxygenases, esterases, and glutathione -transferases) were performed on susceptible and resistant mosquito populations. Wild mosquito populations were identified to species level using polymerase chain reaction (PCR). The species of the wild mosquito populations were identified to species level using PCR. Real-time PCR was performed on the susceptible and resistant mosquitoes after the WHO tube bioassays to determine the presence of knockdown resistance () allele.
WHO susceptibility tests indicated that showed resistance to Pyrethroids and DDT in all the study sites, to Bendiocarb in Iguhu and Kabula and susceptible to Malathion (100% mortality) in all the study sites. There was an elevation of monooxygenases and esterases enzymatic activities in resistant mosquito populations exposed to Lambdacyhalothrin, Permethrin, Deltamethrin and DDT but no elevation in glutathione -transferases. A high frequency of L1014S allele was detected in s.s. population, but there was no kdr allele found in mosquitoes.
mosquitoes from western Kenya have developed phenotypic resistance to pyrethroids and DDT. Therefore, there is a need for further research covering different climatic zones with different agroeconomic activities for detailed report on current status of insecticide resistance in malaria vectors.
在大规模采用多种干预手段后,疟疾媒介控制工作已使每年的疟疾相关病例数降至可观水平。基于杀虫剂的手段仍是肯尼亚控制疟疾媒介的主要选择,因此,此类项目因报告的杀虫剂抗性而受到影响的可能性令人高度担忧。本研究的目的是评估肯尼亚西部不同农业生态系统中疟疾媒介的杀虫剂抗性状况。
研究在肯尼亚西部的低地和高地开展,具体地点有阿赫罗、基西安、楚莱姆博、埃穆泰特、埃马卡哈、伊古胡和卡布拉。使用氯氟氰菊酯、溴氰菊酯、氯菊酯、滴滴涕、残杀威和马拉硫磷的标准诊断剂量,对从阿赫罗、基西安、楚莱姆博、埃穆泰特、埃马卡哈、伊古胡和卡布拉这七个地点采集的蚊子进行世界卫生组织试管生物测定。进行生化测定,对易感和抗性蚊子种群检测三种酶(单加氧酶、酯酶和谷胱甘肽 -转移酶)的酶活性。使用聚合酶链反应(PCR)将野生蚊子种群鉴定到物种水平。在世界卫生组织试管生物测定后,对易感和抗性蚊子进行实时PCR,以确定击倒抗性()等位基因的存在。
世界卫生组织的敏感性测试表明,在所有研究地点均对拟除虫菊酯和滴滴涕表现出抗性,在伊古胡和卡布拉对残杀威表现出抗性,而在所有研究地点对马拉硫磷敏感(死亡率100%)。暴露于氯氟氰菊酯、氯菊酯、溴氰菊酯和滴滴涕的抗性蚊子种群中,单加氧酶和酯酶的酶活性有所升高,但谷胱甘肽 -转移酶没有升高。在冈比亚按蚊种群中检测到高频率的L1014S等位基因,但在致倦库蚊中未发现击倒抗性等位基因。
肯尼亚西部的蚊子已对拟除虫菊酯和滴滴涕产生表型抗性。因此,需要针对具有不同农业经济活动的不同气候区开展进一步研究,以详细报告疟疾媒介中杀虫剂抗性的现状。