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对杀虫剂抗性蚊虫库蚊(双翅目:蚊科)的蚊固醇载体蛋白-2 抑制剂的杀幼虫活性。

Larvicidal activity of mosquito sterol carrier protein-2 inhibitors to the insecticide-resistant mosquito Culex quinquefasciatus (Diptera: Culicidae).

机构信息

Department of Entomology and Plant Pathology, Auburn University, Auburn, AL 36849, USA.

出版信息

J Med Entomol. 2009 Nov;46(6):1430-5. doi: 10.1603/033.046.0626.

Abstract

AeSCP-2 inhibitors (SCPIs) compete with cholesterol for binding to a mosquito sterol carrier protein-2 (AeSCP-2) known to aid in the uptake of cholesterol in mosquito cells. The larvicidal activities of AeSCP-2 inhibitor-1 (SCPI-1) and inhibitor-2 (SCPI-2) against Culex quinquefasciatus Say (Diptera: Culicidae) were therefore examined in insecticide-resistant Culex mosquitoes HAmCq(G9), MAmCq(G2), and BAmCq(G0). All of the resistant Culex mosquito strains exhibited similar sensitivity to SCPI-1 and SCPI-2 inhibitors compared with a susceptible S-Lab strain. When an AeSCP-2 inhibitor was applied simultaneously with permethrin, the toxicity of permethrin to the second-instar larvae of all four strains of Culex mosquitoes increased, suggesting a synergistic effect of AeSCP-2 inhibitors on the toxicity of permethrin against Culex mosquitoes. Both SCPI-1 and SCPI-2 inhibitors caused a 2.4- to 3-fold reduction in the level of permethrin resistance in the highly resistant strain HAmCq(G9). This result suggests that the mode of action of the AeSCP-2 inhibitors, which reduces the uptake of cholesterol by inhibiting the function of AeSCP-2 in mosquito cells, may interfere with the mechanisms or ability that govern permethrin resistance in the HAmCq(G9) mosquito strain.

摘要

AeSCP-2 抑制剂 (SCPIs) 与胆固醇竞争结合到一种蚊子固醇载体蛋白-2 (AeSCP-2),已知该蛋白有助于蚊子细胞摄取胆固醇。因此,研究了 AeSCP-2 抑制剂-1 (SCPI-1) 和抑制剂-2 (SCPI-2) 对埃及伊蚊 HAmCq(G9)、MAmCq(G2) 和 BAmCq(G0) 的幼虫的杀虫活性。与敏感的 S-Lab 株相比,所有抗药性埃及伊蚊株对 SCPI-1 和 SCPI-2 抑制剂均表现出相似的敏感性。当 AeSCP-2 抑制剂与氯菊酯同时应用时,四种埃及伊蚊株的二龄幼虫对氯菊酯的毒性增加,表明 AeSCP-2 抑制剂对氯菊酯对埃及伊蚊的毒性具有协同作用。SCPI-1 和 SCPI-2 抑制剂均使高度抗性的 HAmCq(G9) 株的氯菊酯抗性降低了 2.4 至 3 倍。这一结果表明,AeSCP-2 抑制剂的作用模式,通过抑制 AeSCP-2 在蚊子细胞中的功能来减少胆固醇的摄取,可能会干扰 HAmCq(G9) 蚊株中控制氯菊酯抗性的机制或能力。

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