Functional investigation of a novel and essential subcellular compartment in Plasmodium falciparum transmission stage parasites

恶性疟原虫传播阶段寄生虫中新型重要亚细胞区室的功能研究

基本信息

批准号：
10584525
负责人：
JEFFREY D DVORIN
金额：
$ 75.31万
依托单位：
BOSTON CHILDREN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-03-04 至 2027-02-28
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10584525
关键词：
3-Dimensional 5 year old Biogenesis Biophysics Blood Cell membrane Cellular Morphology Cessation of life Child Complex Culicidae Cytoskeleton Defect Development Electron Microscopy Epitopes Erythrocytes Female Filament Future Gene Proteins Genes Goals Human Image Immunofluorescence Immunologic Infection Ingestion Intermediate Filaments Investigation Ions Knock-out Label Life Cycle Stages Malaria Measures Membrane Microfabrication Microtubules Molecular Morbidity - disease rate Morphology Multiprotein Complexes Names Parasites Pathway interactions Plasmodium falciparum Platinum Population Process Proteins Scanning Electron Microscopy Series Shapes Techniques Testing Transgenic Organisms Transmission Electron Microscopy Vesicle Visualization Width asexual improved knock-down male member mortality novel novel strategies resilience reverse genetics transmission process

项目摘要

PROJECT SUMMARY Malaria is an important cause of illness and death worldwide, with most of these deaths resulting from Plasmodium falciparum infection. Successful completion of the P. falciparum life cycle and infection of a new human host requires transmission. During the asexual blood stage in human red blood cells, a small population of parasites differentiates into transmission forms known as gametocytes. These gametocytes can complete the sexual stage of the parasite life cycle following ingestion by a mosquito. Gametocyte maturation in human red blood cells occurs over 10-12 days and is associated with major changes in cellular morphology and rigidity. A newly discovered protein PfBLEB (for Baso-Lateral Expansion Boundary) is essential for mature gametocyte formation. In asexual parasites, PfBLEB is part of the basal complex, a ring-like multi-protein complex at the leading edge of the inner membrane complex. While PfBLEB is dispensable for both asexual replication and gametocyte commitment, it is essential for gametocyte development. PfBLEB-knockdown or knockout gametocytes arrest during maturation and are non- transmissible. Furthermore, the PfBLEB-deficient gametocytes have gross morphologic changes with defects in major cytoskeletal features of the maturing transmission-stage parasite, including the inner membrane complex and subpellicular microtubules. In gametocytes with normal PfBLEB expression, PfBLEB defines a new subcellular compartment within the parasite, demarcating the regions of the parasite plasma membrane that are devoid of the underlying inner membrane complex. The PfBLEB-compartment is essential for gametocyte development, but the function and protein constituents of this newly discovered subcellular compartment remain unknown. The goal of the current application is to define and genetically evaluate the protein components of the PfBLEB compartment and to understand the functional defects in PfBLEB-deficient gametocytes. The first aim will utilize proximity labeling and reverse genetics to explore the PfBLEB-containing compartment. The second aim will utilize multiple imaging and microfabrication techniques to gain a functional understanding of what processes are abnormal in PfBLEB-deficient gametocytes. Together, the proposed studies will add a new layer to our molecular understanding of gametocyte development in P. falciparum.

项目概要疟疾是全世界疾病和死亡的重要原因，其中大部分死亡是由疟疾引起的恶性疟原虫感染。成功完成恶性疟原虫的生命周期并感染新的人类宿主需要传播。在人类红细胞的无性血液阶段，一个小的寄生虫群体分化成称为配子体的传播形式。这些配子体被蚊子摄入后可以完成寄生虫生命周期的有性阶段。配子体人类红细胞的成熟过程需要 10-12 天，并且与细胞形态和刚性。新发现的蛋白质 PfBLEB（用于基底外侧扩展边界）对于成熟配子体的形成至关重要。在无性寄生虫中，PfBLEB 是基底复合体的一部分，在内膜复合物前沿的环状多蛋白复合物。虽然 PfBLEB 是对于无性复制和配子细胞定型来说都是可有可无的，但它对于配子细胞来说是必不可少的发展。 PfBLEB 敲低或敲除配子细胞在成熟过程中停滞，并且是非可传播的。此外，PfBLEB 缺陷的配子细胞具有明显的形态变化成熟传播阶段寄生虫主要细胞骨架特征的缺陷，包括内部膜复合体和膜下微管。在具有正常 PfBLEB 表达的配子细胞中，PfBLEB 在配子细胞内定义了一个新的亚细胞区室。寄生虫，划分寄生虫质膜的区域，这些区域没有底层的内部膜复合物。 PfBLEB 区室对于配子体发育至关重要，但其功能这个新发现的亚细胞区室的蛋白质成分仍然未知。的目标目前的应用是定义和遗传评估 PfBLEB 隔室的蛋白质成分并了解 PfBLEB 缺陷配子细胞的功能缺陷。第一个目标将利用邻近性标记和反向遗传学来探索包含 PfBLEB 的隔室。第二个目标将利用多种成像和微加工技术，以获得对流程的功能性理解 PfBLEB 缺陷的配子细胞异常。总之，拟议的研究将为我们的研究增添一个新的层面恶性疟原虫配子体发育的分子理解。