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Increased melanizing activity in Anopheles gambiale does not affect development of Plasmodium falciparum

机译:冈比亚按蚊的黑化活动增加并不影响恶性疟原虫的发展

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Serpins are central to the modulation of various innate immune responses in insects and are suspected to influence the outcome of malaria parasite infection in mosquito vectors. Three Anopheles gambiae serpins (SRPN1, -2, and -3) were tested for their ability to inhibit the prophenoloxidase cascade, a key regulatory process in the melanization response. Recombinant SPRN1 and -2 can bind and inhibit a heterologous phenoloxiclase-activating protease and inhibit phenoloxidase activation in vitro. Using a reverse genetics approach, we studied the effect of SRPN2 on melanization in An. gambiae adult females in vivo. Depletion of SRPN2 from the mosquito hemolymph increases melanin deposition on foreign surfaces such as negatively charged Sephadex beads. As reported, the knockdown of SRPN2 adversely affects the ability of the rodent malaria parasite Plasmodium berghei to invade the midgut epithelium and develop into oocysts. Importantly, we tested whether the absence of SRPN2 from the hemolymph influences Plasmodium falciparum development. RNAi silencing of SRPN2 in an An. gambiae strain originally established from local populations in Yaounde, Cameroon, did not influence the development of autochthonous field isolates of P. falciparum. This study suggests immune evasion strategies of the human malaria parasite and emphasizes the need to study mosquito innate immune responses toward the pathogens they transmit in natural vector-parasite combinations.
机译:丝氨酸蛋白酶抑制剂是昆虫中各种先天免疫反应的调节的中心,并且被怀疑会影响蚊媒中疟原虫感染的结果。测试了三个冈比亚按蚊的丝氨酸蛋白酶抑制剂(SRPN1,-2和-3)抑制前酚氧化酶级联反应的能力,后者是黑色素化反应中的关键调控过程。重组SPRN1和-2可以结合并抑制异源酚氧合酶激活蛋白酶,并在体外抑制酚氧化酶激活。使用反向遗传学方法,我们研究了SRPN2对An的黑化的影响。冈比亚成年女性体内。蚊虫淋巴中的SRPN2耗竭会增加黑色素在异物表面(如带负电的Sephadex珠粒)上的沉积。如所报道的,SRPN2的敲低对啮齿动物疟疾寄生虫伯氏疟原虫侵袭中肠上皮并发展为卵囊的能力产生不利影响。重要的是,我们测试了血淋巴中SRPN2的缺失是否会影响恶性疟原虫的发育。 SRPN2 RNAi沉默。最初从喀麦隆雅温得当地人口建立的冈比亚菌株并未影响恶性疟原虫田间分离株的发育。这项研究提出了人类疟疾寄生虫的逃避策略,并强调有必要研究蚊子对以天然载体-寄生虫组合传播的病原体的先天免疫反应。

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