Wolanin Kamil, Fontinha Diana, Sanches-Vaz Margarida, Nyboer Britta, Heiss Kirsten, Mueller Ann-Kristin, Prudêncio Miguel
Parasitology Unit, Centre for Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.
Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
Cell Microbiol. 2019 Oct;21(10):e13088. doi: 10.1111/cmi.13088. Epub 2019 Jul 30.
Intracellular Plasmodium parasites develop inside a parasitophorous vacuole (PV), a specialised compartment enclosed by a membrane (PVM) that contains proteins of both host and parasite origin. Although exported protein 1 (EXP1) is one of the earliest described parasitic PVM proteins, its function throughout the Plasmodium life cycle remains insufficiently understood. Here, we show that whereas the N-terminus of Plasmodium berghei EXP1 (PbEXP1) is essential for parasite survival in the blood, parasites lacking PbEXP1's entire C-terminal (CT) domain replicate normally in the blood but cause less severe pathology than their wild-type counterparts. Moreover, truncation of PbEXP1's CT domain not only impairs parasite development in the mosquito but also abrogates PbEXP1 localization to the PVM of intrahepatic parasites, severely limiting their replication and preventing their egress into the blood. Our findings highlight the importance of EXP1 during the Plasmodium life cycle and identify this protein as a promising target for antiplasmodial intervention.
细胞内疟原虫寄生于一个寄生泡(PV)内,这是一个由膜(PVM)包围的特殊区室,其中含有宿主和寄生虫来源的蛋白质。尽管输出蛋白1(EXP1)是最早被描述的寄生性PVM蛋白之一,但其在疟原虫整个生命周期中的功能仍未得到充分了解。在这里,我们表明,虽然伯氏疟原虫EXP1(PbEXP1)的N端对寄生虫在血液中的存活至关重要,但缺乏PbEXP1整个C端(CT)结构域的寄生虫在血液中能正常复制,但其致病性比野生型对应物轻。此外,PbEXP1的CT结构域截断不仅损害寄生虫在蚊子体内的发育,还消除了PbEXP1在肝内寄生虫PVM上的定位,严重限制了它们的复制并阻止它们进入血液。我们的研究结果突出了EXP1在疟原虫生命周期中的重要性,并将该蛋白确定为抗疟干预的一个有前景的靶点。