Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 9017-CIIL-Center for Infection and Immunity of Lille, Lille, France.
Department of Veterinary Sciences, Experimental Parasitology, Ludwig-Maximilians-Universität, Munich, Germany.
PLoS Pathog. 2020 May 28;16(5):e1008106. doi: 10.1371/journal.ppat.1008106. eCollection 2020 May.
Toxoplasma gondii possesses an armada of secreted virulent factors that enable parasite invasion and survival into host cells. These factors are contained in specific secretory organelles, the rhoptries, micronemes and dense granules that release their content upon host cell recognition. Dense granules are secreted in a constitutive manner during parasite replication and play a crucial role in modulating host metabolic and immune responses. While the molecular mechanisms triggering rhoptry and microneme release upon host cell adhesion have been well studied, constitutive secretion remains a poorly explored aspect of T. gondii vesicular trafficking. Here, we investigated the role of the small GTPase Rab11A, a known regulator of exocytosis in eukaryotic cells. Our data revealed an essential role of Rab11A in promoting the cytoskeleton driven transport of dense granules and the release of their content into the vacuolar space. Rab11A also regulates transmembrane protein trafficking and localization during parasite replication, indicating a broader role of Rab11A in cargo exocytosis at the plasma membrane. Moreover, we found that Rab11A also regulates extracellular parasite motility and adhesion to host cells. In line with these findings, MIC2 secretion was altered in Rab11A-defective parasites, which also exhibited severe morphological defects. Strikingly, by live imaging we observed a polarized accumulation of Rab11A-positive vesicles and dense granules at the apical pole of extracellular motile and invading parasites suggesting that apically polarized Rab11A-dependent delivery of cargo regulates early secretory events during parasite entry into host cells.
刚地弓形虫拥有一系列分泌的毒力因子,使寄生虫能够入侵和在宿主细胞中存活。这些因子包含在特定的分泌细胞器中,即棒状体、微线体和致密颗粒,它们在宿主细胞识别时释放其内容物。致密颗粒在寄生虫复制过程中以组成型方式分泌,在调节宿主代谢和免疫反应方面发挥着至关重要的作用。虽然触发宿主细胞黏附时棒状体和微线体释放的分子机制已经得到了很好的研究,但致密颗粒的组成型分泌仍然是刚地弓形虫囊泡运输中一个探索不足的方面。在这里,我们研究了小 GTPase Rab11A 的作用,Rab11A 是真核细胞中已知的胞吐作用调节剂。我们的数据揭示了 Rab11A 在促进致密颗粒的骨架驱动运输和将其内容物释放到空泡空间中的重要作用。Rab11A 还调节寄生虫复制过程中跨膜蛋白的运输和定位,表明 Rab11A 在质膜上的货物胞吐作用中具有更广泛的作用。此外,我们发现 Rab11A 还调节寄生虫的体外运动和与宿主细胞的黏附。与这些发现一致,Rab11A 缺陷型寄生虫中的 MIC2 分泌发生改变,也表现出严重的形态缺陷。引人注目的是,通过实时成像观察到 Rab11A 阳性囊泡和致密颗粒在体外运动和入侵寄生虫的顶端极的极化积累,这表明顶端极化的 Rab11A 依赖性货物传递调节寄生虫进入宿主细胞时早期分泌事件。