ICMR-National Institute of Malaria Research, Sector-8, Dwarka, New Delhi, 110077, India.
Liverpool School of Tropical Medicine, Liverpool, UK.
Malar J. 2018 Nov 8;17(1):414. doi: 10.1186/s12936-018-2557-1.
Deltamethrin-impregnated, long-lasting insecticidal nets (LLINs) were distributed in the study area from November 2014 to January 2015 to evaluate their impact on malaria transmission in the presence of insecticide-resistant vectors. Studies were carried out in 16 selected clusters in Keshkal sub-district, Chhattisgarh State, India to monitor and characterize deltamethrin resistance in Anopheles culicifacies sensu lato.
Deltamethrin susceptibility of An. culicifacies decreased in a post-LLIN survey compared to a pre-LLIN survey and was not significant (p > 0.05) while, the knockdown values showed significant increase (p < 0.05). Pre-exposure to piperonyl butoxide, triphenyl phosphate showed synergism against deltamethrin (p < 0.001). Biochemical assays showed significantly (p < 0.05) elevated monooxygenases in 3 of 5 clusters in post-LLIN survey-I that increased to 10 of 11 clusters in post-LLIN survey-II, while esterases were found significantly elevated in all clusters and both enzymes were involved in conferring pyrethroid resistance, not discounting the involvement of kdr (L1014L/S) gene that was heterozygous and at low frequency (4-5%).
This field study, in a tribal district of India, after distribution of deltamethrin-impregnated LLINs showed decrease in deltamethrin susceptibility in An. culicifacies, a major vector of malaria in this study area and in India. Results indicated development of resistance as imminent with the increase in insecticide selection pressure. There is an urgent need to develop new vector control tools, with insecticide classes having novel mechanisms of resistance, to avoid or delay the onset of resistance. Regular insecticide resistance monitoring and mechanistic studies should be the priority for the malaria control programmes to suggest strategies for insecticide resistance management. The global commitment to eliminate malaria by 2030 needs various efforts that include development of combination vector control products and interventions and few are becoming available.
从 2014 年 11 月至 2015 年 1 月,在研究区域发放了含增效氯菊酯的长效驱虫蚊帐(LLINs),以评估其对存在抗杀虫剂蚊虫的疟疾传播的影响。在印度恰蒂斯加尔邦凯什卡尔分区的 16 个选定集群中开展了研究,以监测和描述长角按蚊按蚊复合体对氯菊酯的抗性。
与预 LLIN 调查相比,LLIN 后调查中按蚊对氯菊酯的敏感性降低,但差异无统计学意义(p>0.05),而击倒值则显著升高(p<0.05)。预先接触增效醚和磷酸三苯酯对氯菊酯表现出增效作用(p<0.001)。生化检测显示,在 LLIN 后调查-I 的 3 个集群中,单氧化酶显著升高(p<0.05),在 LLIN 后调查-II 的 11 个集群中,单氧化酶均显著升高,而酯酶在所有集群中均显著升高,这两种酶均参与了对拟除虫菊酯的抗性,不能排除 kdr(L1014L/S)基因的参与,该基因呈杂合状态且频率较低(4-5%)。
在印度的一个部落地区进行的这项实地研究表明,在发放了含增效氯菊酯的 LLINs 后,按蚊对氯菊酯的敏感性降低,而按蚊是该研究区域和印度的主要疟疾传播媒介。研究结果表明,随着杀虫剂选择压力的增加,抗药性即将出现。迫切需要开发具有新型抗药性机制的新的病媒控制工具,以避免或延迟抗药性的出现。定期进行杀虫剂抗药性监测和机制研究应成为疟疾控制规划的重点,以提出杀虫剂抗药性管理策略。全球承诺到 2030 年消除疟疾,需要作出各种努力,包括开发组合病媒控制产品和干预措施,其中一些措施正在取得成效。