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Cyclic GMP Balance Is Critical for Malaria Parasite Transmission from the Mosquito to the Mammalian Host

机译:循环GMP平衡对于疟疾从蚊子到哺乳动物宿主的寄生虫传播至关重要

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ABSTRACT Transmission of malaria occurs during Anopheles mosquito vector blood meals, when Plasmodium sporozoites that have invaded the mosquito salivary glands are delivered to the mammalian host. Sporozoites display a unique form of motility that is essential for their movement across cellular host barriers and invasion of hepatocytes. While the molecular machinery powering motility and invasion is increasingly well defined, the signaling events that control these essential parasite activities have not been clearly delineated. Here, we identify a phosphodiesterase ( PDE γ) in Plasmodium , a regulator of signaling through cyclic nucleotide second messengers. Reverse transcriptase PCR (RT-PCR) analysis and epitope tagging of endogenous PDEγ detected its expression in blood stages and sporozoites of Plasmodium yoelii . Deletion of PDE γ ( pde γ~(?)) rendered sporozoites nonmotile, and they failed to invade the mosquito salivary glands. Consequently, PDEγ deletion completely blocked parasite transmission by mosquito bite. Strikingly, pde γ~(?)sporozoites showed dramatically elevated levels of cyclic GMP (cGMP), indicating that a perturbation in cyclic nucleotide balance is involved in the observed phenotypic defects. Transcriptome sequencing (RNA-Seq) analysis of pde γ~(?)sporozoites revealed reduced transcript abundance of genes that encode key components of the motility and invasion apparatus. Our data reveal a crucial role for PDE γ in maintaining the cyclic nucleotide balance in the malaria parasite sporozoite stage, which in turn is essential for parasite transmission from mosquito to mammal. IMPORTANCE Malaria is a formidable threat to human health worldwide, and there is an urgent need to identify novel drug targets for this parasitic disease. The parasite is transmitted by mosquito bite, inoculating the host with infectious sporozoite stages. We show that cellular signaling by cyclic nucleotides is critical for transmission of the parasite from the mosquito vector to the mammalian host. Parasite phosphodiesterase γ is essential for maintaining cyclic nucleotide balance, and its deletion blocks transmission of sporozoites. A deeper understanding of the signaling mechanisms involved in transmission might inform the discovery of novel drugs that interrupt this essential step in the parasite life cycle.
机译:摘要疟疾的传播是在按蚊蚊媒血餐中发生的,当时已将侵袭蚊唾液腺的疟原虫子孢子运送到哺乳动物宿主中。子孢子显示出独特的运动形式,这对于它们跨细胞宿主屏障运动和侵袭肝细胞至关重要。尽管驱动动力和侵袭的分子机制越来越明确,但控制这些基本寄生虫活动的信号传递事件尚未明确描述。在这里,我们确定了疟原虫中的磷酸二酯酶(PDEγ),它是通过环状核苷酸第二信使的信号调节剂。内源性PDEγ的逆转录酶PCR(RT-PCR)分析和表位标记检测到了其在约氏疟原虫血液阶段和子孢子中的表达。 PDEγ(pdeγ〜(?))的缺失使子孢子不能运动,它们不能侵入蚊子唾液腺。因此,PDEγ缺失完全阻止了蚊虫叮咬的寄生虫传播。令人惊讶的是,pdeγ〜(β)子孢子的环GMP(cGMP)含量显着升高,表明观察到的表型缺陷涉及环核苷酸平衡的扰动。对pdeγ〜(?)子孢子的转录组测序(RNA-Seq)分析显示,编码运动和入侵装置关键成分的基因的转录丰度降低。我们的数据揭示了PDEγ在疟疾寄生虫子孢子阶段维持环状核苷酸平衡中的关键作用,而这反过来又是寄生虫从蚊子传播到哺乳动物所必需的。重要信息疟疾是对全世界人类健康的巨大威胁,因此迫切需要确定这种寄生虫病的新型药物靶标。寄生虫通过蚊虫叮咬传播,从而使宿主感染了子孢子。我们表明,环核苷酸的细胞信号传导对于从蚊子载体到哺乳动物宿主的寄生虫传播至关重要。寄生虫磷酸二酯酶γ对于维持环状核苷酸平衡是必不可少的,其缺失会阻止子孢子的传播。对传播中涉及的信号传导机制的更深入的了解可能会为发现新药打扰寄生虫生命周期中这一必不可少的步骤提供信息。

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