Larson Ryan T, Wessely Vilena, Jiang Zhisheng, Lan Que
Department of Entomology, University of Wisconsin-Madison, Madison, WI 53706, USA.
J Med Entomol. 2008 May;45(3):439-44. doi: 10.1603/0022-2585(2008)45[439:laoscp]2.0.co;2.
A previous report has shown that mosquito sterol carrier protein-2 inhibitors (SCPIs) are larvicidal to larvae of the yellowfever mosquito, Aedes aegypti (L.) (J. Lipid Res. 46: 650-657, 2005). In the current study, we tested SCPI-1 in an additional four mosquito species for larvicidal activities: Culex pipiens pipiens, Anopheles gambiae, Culex restuans, and Aedes vexans. Cholesterol accumulation in SCPI-treated Ae. aegypti fourth instars was examined. SCPI-1 is lethal to all tested mosquito species, with the LC50 value ranging from 5.2 to 15 microM when treatments started at the first to third instar. However, LC50 values increase to from 5.2 to 38.7 microM in treatments started at first and fourth instar, respectively. The results indicate that the lethal effect of SCPI-1 decreases with the growth of larvae, which suggests that SCPI-1 is more effective before the larvae reach final growth period (the last instar). SCPI-1 suppressed cholesterol uptake in Ae. aegypti fourth instars, suggesting that one of the modes of action of SCPI-1 is via reduction in cholesterol absorption.
先前的一份报告显示,蚊虫固醇载体蛋白2抑制剂(SCPIs)对黄热病蚊虫埃及伊蚊(Aedes aegypti (L.))的幼虫具有杀幼虫活性(《脂质研究杂志》46: 650 - 657, 2005)。在当前研究中,我们在另外四种蚊虫中测试了SCPI - 1的杀幼虫活性:致倦库蚊(Culex pipiens pipiens)、冈比亚按蚊(Anopheles gambiae)、骚扰库蚊(Culex restuans)和刺扰伊蚊(Aedes vexans)。我们检测了经SCPI处理的埃及伊蚊四龄幼虫中的胆固醇积累情况。SCPI - 1对所有测试的蚊虫种类均具有致死性,当从一龄至三龄开始处理时,其LC50值范围为5.2至15微摩尔。然而,当分别从一龄和四龄开始处理时,LC50值分别增至5.2至38.7微摩尔。结果表明,SCPI - 1的致死作用随幼虫生长而降低,这表明SCPI - 1在幼虫达到最终生长阶段(末龄)之前更有效。SCPI - 1抑制了埃及伊蚊四龄幼虫对胆固醇的摄取,这表明SCPI - 1的作用模式之一是通过减少胆固醇吸收。