Department of Parasitology, Faculty of Medicine, University Malaya, Kuala Lumpur, 50603, Malaysia.
The Tropical Infectious Diseases Research and Education Centre (TIDREC), Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Parasit Vectors. 2019 May 16;12(1):236. doi: 10.1186/s13071-019-3472-1.
Dengue is a serious public health problem worldwide, including in Selangor, Malaysia. Being an important vector of dengue virus, Aedes aegypti are subjected to control measures which rely heavily on the usage of insecticides. Evidently, insecticide resistance in Ae. aegypti, which arise from several different point mutations within the voltage-gated sodium channel genes, has been documented in many countries. Thus, this robust study was conducted in all nine districts of Selangor to understand the mechanisms of resistance to various insecticides in Ae. aegypti. Mosquitoes were collected from dengue epidemic and non-dengue outbreak areas in Selangor.
Using the Center for Disease Control and Prevention (CDC) bottle assays, the insecticide resistance status of nine different Ae. aegypti strains from Selangor was accessed. Synergism tests and biochemical assays were conducted to further understand the metabolic mechanisms of insecticide resistance. Polymerase chain reaction (PCR) amplification and sequencing of the IIP-IIS6 as well as IIIS4-IIIS6 regions of the sodium channel gene were performed to enable comparisons between susceptible and resistant mosquito strains. Additionally, genomic DNA was used for allele-specific PCR (AS-PCR) genotyping of the gene to detect the presence of F1534C, V1016G and S989P mutations.
Adult female Ae. aegypti from various locations were susceptible to malathion and propoxur. However, they exhibited different levels of resistance against dichlorodiphenyltrichloroethane (DDT) and pyrethroids. The results of synergism tests and biochemical assays indicated that the mixed functions of oxidases and glutathione S-transferases contributed to the DDT and pyrethroid resistance observed in the present study. Besides detecting three single kdr mutations, namely F1534C, V1016G and S989P, co-occurrence of homozygous V1016G/S989P (double allele) and F1534C/V1016G/S989P (triple allele) mutations were also found in Ae. aegypti. As per the results, the three kdr mutations had positive correlations with the expressions of resistance to DDT and pyrethroids.
In view of the above outcomes, it is important to seek new tools for vector management instead of merely relying on insecticides. If the latter must be used, regular monitoring of insecticide resistance should also be carried out at all dengue epidemic areas. Since the eggs of Ae. aegypti can be easily transferred from one location to another, it is probable that insecticide-resistant Ae. aegypti can be found at non-dengue outbreak sites as well.
登革热是一个严重的全球公共卫生问题,包括在马来西亚雪兰莪州。埃及伊蚊作为登革热病毒的重要载体,受到了严重依赖杀虫剂使用的控制措施的影响。显然,在许多国家都记录了埃及伊蚊中由于电压门控钠离子通道基因中的几个不同点突变而产生的杀虫剂抗性。因此,在雪兰莪州的九个地区进行了这项强有力的研究,以了解埃及伊蚊对各种杀虫剂的抗性机制。蚊子是从雪兰莪州的登革热流行区和非登革热暴发区收集的。
使用疾病控制和预防中心(CDC)瓶试验,评估了来自雪兰莪州的 9 种不同埃及伊蚊菌株的杀虫剂抗性状况。进行增效试验和生化分析,以进一步了解杀虫剂抗性的代谢机制。对钠离子通道基因的 IIP-IIS6 以及 IIIS4-IIIS6 区域进行聚合酶链反应(PCR)扩增和测序,以比较敏感和抗性蚊株。此外,使用基因组 DNA 进行基因的等位基因特异性 PCR(AS-PCR)基因分型,以检测 F1534C、V1016G 和 S989P 突变的存在。
来自不同地点的成年雌性埃及伊蚊对马拉硫磷和丙硫磷敏感。然而,它们对滴滴涕和拟除虫菊酯表现出不同程度的抗性。增效试验和生化分析的结果表明,混合功能氧化酶和谷胱甘肽 S-转移酶对本研究中观察到的滴滴涕和拟除虫菊酯抗性有贡献。除了检测到三个单 kdr 突变,即 F1534C、V1016G 和 S989P 之外,还发现埃及伊蚊中存在纯合 V1016G/S989P(双等位基因)和 F1534C/V1016G/S989P(三等位基因)突变的共发生。根据结果,这三个 kdr 突变与滴滴涕和拟除虫菊酯的抗性表达呈正相关。
鉴于上述结果,有必要寻求新的媒介管理工具,而不仅仅是依赖杀虫剂。如果必须使用后者,还应在所有登革热流行地区定期监测杀虫剂抗性。由于埃及伊蚊的卵很容易从一个地点转移到另一个地点,因此在非登革热暴发地区也可能发现对杀虫剂有抗性的埃及伊蚊。