Silva Ana Paula B, Santos Joselita Maria M, Martins Ademir J
Laboratório de Fisiologia e Controle de Artrópodes Vetores, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Parasit Vectors. 2014 Oct 7;7:450. doi: 10.1186/1756-3305-7-450.
Constant and extensive use of chemical insecticides has created a selection pressure and favored resistance development in many insect species worldwide. One of the most important pyrethroid resistance mechanisms is classified as target site insensitivity, due to conformational changes in the target site that impair a proper binding of the insecticide molecule. The voltage-gated sodium channel (NaV) is the target of pyrethroids and DDT insecticides, used to control insects of medical, agricultural and veterinary importance, such as anophelines. It has been reported that the presence of a few non-silent point mutations in the NaV gene are associated with pyrethroid resistance, termed as 'kdr' (knockdown resistance) for preventing the knockdown effect of these insecticides. The presence of these mutations, as well as their effects, has been thoroughly studied in Anopheles mosquitoes. So far, kdr mutations have already been detected in at least 13 species (Anopheles gambiae, Anopheles arabiensis, Anopheles sinensis, Anopheles stephensi, Anopheles subpictus, Anopheles sacharovi, Anopheles culicifacies, Anopheles sundaicus, Anopheles aconitus, Anopheles vagus, Anopheles paraliae, Anopheles peditaeniatus and Anopheles albimanus) from populations of African, Asian and, more recently, American continents. Seven mutational variants (L1014F, L1014S, L1014C, L1014W, N1013S, N1575Y and V1010L) were described, with the highest prevalence of L1014F, which occurs at the 1014 site in NaV IIS6 domain. The increase of frequency and distribution of kdr mutations clearly shows the importance of this mechanism in the process of pyrethroid resistance. In this sense, several species-specific and highly sensitive methods have been designed in order to genotype individual mosquitoes for kdr in large scale, which may serve as important tolls for monitoring the dynamics of pyrethroid resistance in natural populations. We also briefly discuss investigations concerning the course of Plasmodium infection in kdr individuals. Considering the limitation of insecticides available for employment in public health campaigns and the absence of a vaccine able to brake the life cycle of the malaria parasites, the use of pyrethroids is likely to remain as the main strategy against mosquitoes by either indoor residual spraying (IR) and insecticide treated nets (ITN). Therefore, monitoring insecticide resistance programs is a crucial need in malaria endemic countries.
化学杀虫剂的持续广泛使用已形成一种选择压力,并促使全球许多昆虫物种产生抗药性。最重要的拟除虫菊酯抗性机制之一被归类为靶标位点不敏感,这是由于靶标位点的构象变化损害了杀虫剂分子的正常结合。电压门控钠通道(NaV)是拟除虫菊酯和滴滴涕杀虫剂的靶标,这些杀虫剂用于控制具有医学、农业和兽医重要性的昆虫,如按蚊。据报道,NaV基因中一些非同义点突变的存在与拟除虫菊酯抗性相关,这些突变被称为“击倒抗性”(kdr),可防止这些杀虫剂产生击倒作用。这些突变的存在及其影响已在按蚊中得到充分研究。到目前为止,已在非洲、亚洲以及最近在美洲大陆的种群中至少13种按蚊(冈比亚按蚊、阿拉伯按蚊、中华按蚊、斯氏按蚊、伪杂鳞库蚊、萨氏按蚊、库氏按蚊、苏门答腊按蚊、乌头按蚊、迷走按蚊、海滨按蚊、带足按蚊和白跗按蚊)中检测到kdr突变。已描述了七种突变变体(L1014F、L1014S、L1014C、L1014W、N1013S、N1575Y和V1010L),其中L1014F的发生率最高,它发生在NaV IIS6结构域的第1014位点。kdr突变频率和分布的增加清楚地表明了这种机制在拟除虫菊酯抗性过程中的重要性。从这个意义上说,已经设计了几种物种特异性且高度灵敏的方法,以便大规模对单个蚊子进行kdr基因分型,这可作为监测自然种群中拟除虫菊酯抗性动态的重要工具。我们还简要讨论了关于携带kdr突变个体中疟原虫感染过程的研究。考虑到公共卫生运动中可用杀虫剂的局限性以及缺乏能够阻断疟原虫生命周期的疫苗,通过室内滞留喷洒(IR)和经杀虫剂处理的蚊帐(ITN)使用拟除虫菊酯可能仍将是防治蚊子的主要策略。因此,监测杀虫剂抗性计划是疟疾流行国家的一项迫切需求。