Department of Entomology, University of California, Riverside, 92521, USA.
EMBO Rep. 2011 Sep 1;12(9):938-43. doi: 10.1038/embor.2011.130.
Microbial infections in the mosquito Aedes aegypti activate the newly identified CLSP1 and CLSP2 genes, which encode modular proteins composed of elastase-like serine protease and C-type lectin domains. These genes are predominantly regulated by the immune deficiency pathway, but also by the Toll pathway. Silencing of CLSP2, but not CLSP1, results in the activation of prophenoloxidase (PPO), the terminal enzyme in the melanization cascade, suggesting that CLSP2 is a negative modulator of this reaction. Haemolymph PPO activation is normally inhibited in the presence of Plasmodium parasites, but in CLSP2-depleted mosquitoes, the Plasmodium-induced block of melanization is reverted, and these mosquitoes are refractory to the parasite. Thus, CLSP2 is a new component of the mosquito immune response.
在蚊子埃及伊蚊中,微生物感染会激活新发现的 CLSP1 和 CLSP2 基因,这些基因编码由弹性蛋白酶样丝氨酸蛋白酶和 C 型凝集素结构域组成的模块化蛋白。这些基因主要受免疫缺陷途径调控,但也受 Toll 途径调控。沉默 CLSP2,但不沉默 CLSP1,会导致酚氧化酶原 (PPO)的激活,PPO 是黑化级联反应的末端酶,这表明 CLSP2 是该反应的负调节剂。在存在疟原虫寄生虫的情况下,血淋巴 PPO 的激活通常受到抑制,但在 CLSP2 耗尽的蚊子中,疟原虫诱导的黑化阻断被逆转,这些蚊子对寄生虫具有抗性。因此,CLSP2 是蚊子免疫反应的一个新组成部分。