National Institute of Malaria Research, Sector 8, Dwarka, Delhi, 110077, India.
Department of Life Sciences, Jnanabharathi Campus, Bangalore University, Bengaluru, 560056, India.
Parasit Vectors. 2020 Jun 29;13(1):327. doi: 10.1186/s13071-020-04201-3.
Aedes aegypti is a primary vector of dengue, chikungunya and Zika infections in India. In the absence of specific drugs or safe and effective vaccines for these infections, their control relies mainly on vector control measures. The emergence of insecticide resistance in vectors, especially against pyrethroids, is a serious threat to the insecticide-based vector control programme. This study reports the presence of multiple knockdown resistance (kdr) mutations present in an Ae. aegypti population from Bengaluru (India), including a new mutation F1534L.
Aedes aegypti collected from Bengaluru were subjected to insecticide susceptibility tests with DDT, deltamethrin and permethrin. The DNA sequencing of partial domain II, III and IV of the voltage-gated sodium channel (VGSC) was performed to screen kdr mutations present in the population and PCR-based assays were developed for their detection. Genotyping of kdr mutations was done using PCR-based assays, allelic frequencies were determined, and tests of genetic association of kdr mutations with the insecticide resistance phenotype were performed.
The Ae. aegypti population was resistant to DDT, deltamethrin and permethrin. The DNA sequencing of the VGSC revealed the presence of four kdr mutations, i.e. S989P and V1016G in domain II and two alternative kdr mutations F1534C and F1534L in domain III. Allele-specific PCR assays (ASPCR) were developed for the detection of kdr mutations S989P and V1016G and an existing PCR-RFLP based strategy was modified for the genotyping of all three known kdr mutations in domain III (F1534L, F1534C and T1520I). Genotyping of Ae. aegypti samples revealed a moderate frequency of S989P/V1016G (18.27%) and F1534L (17.48%), a relatively high frequency of F1534C (50.61%) and absence of T1520I in the population. Mutations S989P and V1016G were in complete linkage disequilibrium in this population while they were in linkage equilibrium with kdr mutations F1534C and F1534L. The alleles F1534C and F1534L are genetically associated with permethrin resistance.
A new kdr mutation, F1534L, was found in an Ae. aegypti population from Bengaluru (India), co-occurring with the other three mutations S989P, V1016G and F1534C. The findings of a new mutation have implications for insecticide resistance management.
埃及伊蚊是印度登革热、基孔肯雅热和寨卡病毒感染的主要传播媒介。由于这些感染没有特定的药物或安全有效的疫苗,因此它们的控制主要依赖于病媒控制措施。媒介对杀虫剂的抗药性的出现,特别是对拟除虫菊酯类杀虫剂的抗药性,是对基于杀虫剂的病媒控制计划的严重威胁。本研究报告了来自印度班加罗尔的埃及伊蚊种群中存在多种击倒抗性(kdr)突变,包括新的突变 F1534L。
用滴滴涕、溴氰菊酯和氯菊酯对来自班加罗尔的埃及伊蚊进行了杀虫剂敏感性测试。对电压门控钠离子通道(VGSC)的部分域 II、III 和 IV 进行 DNA 测序,以筛选种群中存在的 kdr 突变,并开发了基于 PCR 的检测方法。使用基于 PCR 的检测方法对 kdr 突变进行基因分型,确定等位基因频率,并对 kdr 突变与杀虫剂抗性表型的遗传关联进行了测试。
埃及伊蚊种群对滴滴涕、溴氰菊酯和氯菊酯均有抗性。VGSC 的 DNA 测序显示存在 4 种 kdr 突变,即域 II 中的 S989P 和 V1016G,以及域 III 中的两个替代 kdr 突变 F1534C 和 F1534L。开发了等位基因特异性 PCR 检测方法(ASPCR)用于检测 kdr 突变 S989P 和 V1016G,并修改了现有的基于 PCR-RFLP 的策略,用于对域 III 中所有三种已知的 kdr 突变(F1534L、F1534C 和 T1520I)进行基因分型。对埃及伊蚊样本的基因分型显示,S989P/V1016G(18.27%)和 F1534L(17.48%)的频率中等,F1534C(50.61%)的频率相对较高,而种群中不存在 T1520I。该种群中 S989P 和 V1016G 完全处于连锁不平衡状态,而它们与 kdr 突变 F1534C 和 F1534L 处于连锁平衡状态。等位基因 F1534C 和 F1534L 与拟除虫菊酯抗性遗传相关。
在来自印度班加罗尔的埃及伊蚊种群中发现了一种新的 kdr 突变 F1534L,与其他三种突变 S989P、V1016G 和 F1534C 同时存在。新突变的发现对杀虫剂抗性管理具有重要意义。