印度埃及伊蚊种群的抗敲低(kdr)突变:携带V1016G、F1534C和F1534L kdr等位基因的单倍型缺乏重组

IF 3.4 2区 医学 Q1 PARASITOLOGY
PLoS Neglected Tropical Diseases Pub Date : 2025-06-13 eCollection Date: 2025-06-01 DOI:10.1371/journal.pntd.0013126
Taranjeet Kaur, Rajababu S Kushwah, Sabyasachi Pradhan, Manoj K Das, Madhavinadha P Kona, Anushrita, Radhika Mittal, David Weetman, Rajnikant Dixit, Om P Singh
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引用次数: 0

摘要

背景:电压门控钠通道(VGSC)基因的敲低抗性(Knockdown resistance, kdr)突变是蚊子产生杀虫剂抗性的关键机制。在亚洲埃及伊蚊种群中,已鉴定出两个主要的kdr突变VGSC单倍群:一个携带F1534C突变,另一个携带V1016G和/或S989P突变。先前的功能研究表明,单个单倍型上的这三种突变使拟除虫菊酯抗性增加了1100倍,强调了在不同人群中监测这三种突变的重要性。本研究调查了印度人群中kdr突变的患病率,并探讨了这些突变与位于外显子20和21之间的两种不同保守类型的内含子之间的连锁关联。方法:Ae。利用基于pcr的检测方法,对从8个不同地点收集的埃及伊蚊标本进行了kdr等位基因和内含子(在外显子20和21之间)单倍型的基因分型。对代表性样本进行VGSC区域DNA测序。结果:共鉴定出5个kdr突变,分别为S989P、V1016G、T1520I、F1534C和F1534L,它们在不同地理区域的分布和频率各不相同。在外显子20和21之间鉴定出两种不同且稳定分化的内含子单倍型,称为内含子a和内含子b。在印度人群中观察到七种单倍型,包括两种野生型变体。携带kdr的单倍型可分为三个不同的单倍群:单倍群G (V1016G含/不含S989P和内含子a),单倍群L (F1534L和内含子a)和单倍群C (F1534C含/不含T1520I和内含子b)。重要的是,在这三个单倍群中没有发现在印度人群中重组的证据。结论:在印度伊蚊的VGSC中鉴定出5个kdr突变。埃及伊蚊种群,每个种群都显示出与两种内含子单倍型之一的明确联系。携带989P、1534C和1534L突变的1016G单倍型之间缺乏重组,这表明携带三重kdr突变的最有效的杀虫剂抗性单倍型目前不存在。这一发现具有重大的操作意义,因为它可能表明,目前的病媒控制措施对这些种群仍然有效,可能推迟高度耐药表型的出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knockdown-resistance (kdr) mutations in Indian Aedes aegypti populations: Lack of recombination among haplotypes bearing V1016G, F1534C, and F1534L kdr alleles.

Background: Knockdown resistance (kdr) mutations in the voltage-gated sodium channel (VGSC) gene are a key mechanism of insecticide resistance in mosquitoes. In Asian Aedes aegypti populations two main VGSC haplogroups with kdr mutations have been identified: one carrying the F1534C mutation and another with V1016G and/or S989P mutations. Previous functional studies have demonstrated that these three mutations on a single haplotype confer up to a 1100-fold increase in pyrethroid resistance, underscoring the importance of monitoring these triple mutations in distinct populations. This study investigates the prevalence of kdr mutations in Indian populations and explores the linkage association between these mutations and two distinct conserved types of introns located between exons 20 and 21.

Methods: Ae. aegypti specimens collected from eight different locations were genotyped for kdr alleles and intron (between exons 20 and 21) haplotypes using PCR-based assays. Representative samples underwent DNA sequencing of VGSC regions.

Results: Five kdr mutations namely S989P, V1016G, T1520I, F1534C, and F1534L were identified, each exhibiting varying distribution and frequencies across different geographical regions. Two distinct and stably-diverged intron haplotypes, designated as intron-A and intron-B, were identified between exons 20 and 21. Seven haplotypes, including two wild-type variants, were observed among Indian populations. The kdr-bearing haplotypes can be classified into three distinct haplogroups: haplogroup G (V1016G with/or without S989P and with intron-A), haplogroup L (F1534L and intron-A), and haplogroup C (F1534C with/or without T1520I and with intron-B). Importantly, no evidence of recombination within Indian populations was detected among these three haplogroups.

Conclusions: Five kdr mutations were identified in the VGSC of Indian Ae. aegypti populations, each showing a definitive linkage with one of the two types of intron haplotypes. The lack of recombination among haplogroups bearing 1016G with 989P, 1534C and 1534L mutations suggests that the most potent insecticide resistance haplotype, bearing the triple kdr mutation, is currently absent. This finding has significant operational implications, as it may indicate that current vector control measures remain effective against these populations, potentially delaying the emergence of highly resistant phenotypes.

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PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases PARASITOLOGY-TROPICAL MEDICINE
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期刊介绍: PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy. The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability. All aspects of these diseases are considered, including: Pathogenesis Clinical features Pharmacology and treatment Diagnosis Epidemiology Vector biology Vaccinology and prevention Demographic, ecological and social determinants Public health and policy aspects (including cost-effectiveness analyses).
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