Perera M Devika B, Hemingway Janet, Karunaratne Shp Parakrama
Department of Zoology, Faculty of Science, University of Peradeniya, Peradeniya, Sri Lanka.
Malar J. 2008 Aug 28;7:168. doi: 10.1186/1475-2875-7-168.
The current status of insecticide resistance and the underlying resistance mechanisms were studied in the major vector of malaria, Anopheles culicifacies, and the secondary vector, Anopheles subpictus in five districts (Anuradhapura, Kurunegala, Moneragala, Puttalam and Trincomalee) of Sri Lanka. Eight other anophelines, Anopheles annularis, Anopheles barbirostris, Anopheles jamesii, Anopheles nigerrimus, Anopheles peditaeniatus, Anopheles tessellatus, Anopheles vagus and Anopheles varuna from Anuradhapura district were also tested.
Adult females were exposed to the WHO discriminating dosages of DDT, malathion, fenitrothion, propoxur, lambda-cyhalothrin, cyfluthrin, cypermethrin, deltamethrin, permethrin and etofenprox. The presence of metabolic resistance by esterase, glutathione S-transferase (GST) and monooxygenase-based mechanisms, and the sensitivity of the acetylcholinesterase target site were assessed using synergists, and biochemical, and metabolic techniques.
All the anopheline species had high DDT resistance. All An. culicifacies and An. subpictus populations were resistant to malathion, except An. culicifacies from Kurunegala, where there was no malathion carboxylesterase activity. Kurunegala and Puttalam populations of An. culicifacies were susceptible to fenitrothion. All the An. culicifacies populations were susceptible to carbamates. Both species were susceptible to the discriminating dosages of cypermethrin and cyfluthrin, but had different levels of resistance to other pyrethroids. Of the 8 other anophelines, only An. nigerrimus and An. peditaeniatus were resistant to all the insecticides tested, probably due to their high exposure to the insecticides used in agriculture. An. vagus showed some resistance to permethrin.Esterases, GSTs and monooxygenases were elevated in both An. culicifacies and An. subpictus. AChE was most sensitive to insecticides in Kurunegala and Trincomalee An. culicifacies populations and highly insensitive in the Trincomalee An. subpictus population.
The complexity of the resistance segregating in these field populations underlines the need for new molecular tools to identify the genomic diversity, differential upregulation and different binding specificities of resistance conferring genes, and the presence of different subspecies with different vectorial capacities.
在斯里兰卡的五个地区(阿努拉德普勒、库鲁内格勒、莫内勒格勒、普塔勒姆和亭可马里),对疟疾主要传播媒介库氏按蚊以及次要传播媒介伪威氏按蚊的杀虫剂抗性现状及其潜在抗性机制进行了研究。还对来自阿努拉德普勒地区的其他八种按蚊,即环纹按蚊、须喙按蚊、杰氏按蚊、黑须按蚊、带足按蚊、鳞斑按蚊、迷走按蚊和瓦氏按蚊进行了测试。
将成年雌蚊暴露于世界卫生组织规定的滴滴涕、马拉硫磷、杀螟硫磷、残杀威、氯氟氰菊酯、氟氯氰菊酯、氯氰菊酯、溴氰菊酯、氯菊酯和醚菊酯的鉴别剂量下。使用增效剂、生化和代谢技术评估酯酶、谷胱甘肽 S -转移酶(GST)和基于单加氧酶的机制引起的代谢抗性,以及乙酰胆碱酯酶靶位点的敏感性。
所有按蚊种类对滴滴涕均具有高抗性。除了来自库鲁内格勒的库氏按蚊(该地区不存在马拉硫磷羧酸酯酶活性)外,所有库氏按蚊和伪威氏按蚊种群对马拉硫磷均有抗性。库氏按蚊在库鲁内格勒和普塔勒姆的种群对杀螟硫磷敏感。所有库氏按蚊种群对氨基甲酸酯类敏感。这两个种类对氯氰菊酯和氟氯氰菊酯的鉴别剂量均敏感,但对其他拟除虫菊酯类的抗性水平不同。在其他八种按蚊中,只有黑须按蚊和带足按蚊对所有测试杀虫剂均有抗性,这可能是由于它们大量接触了农业中使用的杀虫剂。迷走按蚊对氯菊酯表现出一定抗性。酯酶、GST 和单加氧酶在库氏按蚊和伪威氏按蚊中均有所升高。乙酰胆碱酯酶在库鲁内格勒和亭可马里的库氏按蚊种群中对杀虫剂最为敏感,而在亭可马里的伪威氏按蚊种群中高度不敏感。
这些野外种群中抗性分离的复杂性凸显了需要新的分子工具来识别赋予抗性基因的基因组多样性、差异上调和不同结合特异性,以及具有不同媒介能力的不同亚种的存在。