Department of Microbiology and Immunology, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, United States.
Front Immunol. 2018 Nov 21;9:2699. doi: 10.3389/fimmu.2018.02699. eCollection 2018.
Schistosomes exhibit profound developmental adaptations in response to the immune status of their mammalian host, including significant attenuation of parasite growth, development and reproduction in response to deficits in host adaptive immunity. These observations led us to hypothesize that schistosomes regulate the utilization of energy resources in response to immunological conditions within the host. To test this hypothesis, we identified and characterized the AMP-activated protein kinase (AMPK), a heterotrimeric enzyme complex that is central to regulating energy metabolism at the cellular and organismal level in eukaryotes. We show that expression of the catalytic α subunit is developmentally regulated during the parasite life cycle, with peak expression occurring in adult worms. However, the protein is present and phosphorylated in all life cycle stages examined, suggesting a need for active regulation of energy resources throughout the life cycle. In contrast, transcription of the AMPK α gene is down-regulated in cercariae and schistosomula, suggesting that the protein in these life cycle stages is pre-synthesized in the sporocyst and that expression must be re-initiated once inside the mammalian host. We also show that schistosome AMPK α activity in adult worms is sensitive to changes in the parasite's environment, suggesting a mechanism by which schistosome metabolism may be responsive to host immune factors. Finally, we show that AMPK α expression is significantly down-regulated in parasites isolated from immunodeficient mice, suggesting that modulation of parasite energy metabolism may contribute to the attenuation of schistosome growth and reproduction in immunodeficient hosts. These findings provide insights into the molecular interactions between schistosomes and their vertebrate hosts and suggest that parasite energy metabolism may represent a novel target for anti-schistosome interventions.
曼森血吸虫在其哺乳动物宿主的免疫状态下表现出深刻的发育适应,包括寄生虫生长、发育和繁殖的显著衰减,以应对宿主适应性免疫的缺陷。这些观察结果使我们假设曼森血吸虫调节其在宿主内的免疫条件下利用能源的能力。为了验证这一假设,我们鉴定并描述了 AMP 激活蛋白激酶(AMPK),这是一种异三聚体酶复合物,在真核生物中是调节细胞和机体水平能量代谢的核心。我们表明,催化α亚基的表达在寄生虫生活史中是发育调节的,在成虫中表达峰值最高。然而,在所有检查的生活史阶段都存在并磷酸化该蛋白,表明在整个生活史中都需要对能源进行积极的调节。相比之下,AMPKα基因的转录在尾蚴和童虫中被下调,这表明这些生活史阶段的蛋白质在孢子囊中预先合成,并且一旦进入哺乳动物宿主,表达必须重新开始。我们还表明,成虫中曼森血吸虫 AMPKα的活性对寄生虫环境的变化敏感,这表明曼森血吸虫代谢可能对宿主免疫因子有反应的机制。最后,我们表明,从免疫缺陷小鼠中分离的寄生虫中 AMPKα的表达显著下调,这表明寄生虫能量代谢的调节可能有助于衰减免疫缺陷宿主中的曼森血吸虫生长和繁殖。这些发现为曼森血吸虫与其脊椎动物宿主之间的分子相互作用提供了新的认识,并表明寄生虫的能量代谢可能是抗曼森血吸虫干预的一个新靶点。