Microsporidia: invasion apparatus

微孢子虫：入侵装置

• 批准号: 9913441
• 负责人: Louis M. Weiss
• 金额: $ 41.75万
• 依托单位: ALBERT EINSTEIN COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-05-16 至 2021-06-17
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9913441
• 关键词: Acquired Immunodeficiency Syndrome; Agriculture; Animal Feed; Animals; Antibodies; Aquaculture; Area; Benign; Binding; Bioinformatics; Biological; Birds; Category B pathogen; Cell membrane; Cells; Cellular Structures; Cellular biology; Cessation of life; Collaborations; Comparative Study; Complement; Complex; Conjunctivitis; Data; Development; Diarrhea; Economics; Electrons; Encephalitis; Encephalitozoon hellem; Enterocytozoon bieneusi; Epitopes; Fishes; Food; Genetic; Genome; Germination; HIV; Host-Parasite Relations; Human; Immune; Immunization; Immunocompetent; Immunoelectron Microscopy; Immunologics; In Vitro; Infection; Insecta; Invaded; Invertebrates; Investigation; Keratoconjunctivitis; Laboratories; Laboratory Research; Location; Mammals; Manuscripts; Methods; Microbe; Microscopic; Microscopy; Microsporidia; Microsporidiosis; Molecular; Molecular Analysis; Morphology; Mus; Myositis; Nematoda; Nervous system structure; Nosema; Nosema corneum; Organ Transplantation; Organelles; Organism; Parasites; Pathogenesis; Pathogenicity; Patients; Penetration; Phylogenetic Analysis; Post-Translational Protein Processing; Preparation; Process; Proteins; Proteome; Proteomics; Publishing; Receptor Cell; Recombinants; Reproduction spores; Research; Research Project Grants; Respiratory Muscles; Role; Septata intestinalis; Sister; Site; Soil; Source; Structural Protein; Structure; System; Techniques; Transfection; Tube; United States National Institutes of Health; Validation; Water; base; economic impact; experimental study; fungus; gastrointestinal; gene function; genome resource; human pathogen; immunomodulatory therapies; infection management; insight; interest; novel therapeutic intervention; parasite invasion; pathogen; pathogen genome; preservation; programs; protein structure; public health relevance; receptor; reproductive; sample fixation; structural biology; sugar; tool; transcriptome sequencing

ABSTRACT Microsporidia are remarkable parasites related to the Fungi that have been studied for more than 150 years. They are remarkable in their exploitation of all animals ranging from cryptic, benign infections to spectacular, massive infections that cause extensive damage and often death of the host. Microsporidai are opportunistic pathogens in patients with AIDS most commontly causing diarrhea, encephalitis, myositis, or conjunctivitis. Microsporidia can also cause infections in other immune compromised hosts, such as patients who have undergone organ transplantation or those on immune modulating therapies. They are also capable of infecting immune competent hosts most commonly causing keratoconjunctivitis or diarrhea. These pathogenic organisms are classified as NIH category B priority pathogens and EPA pathogens of interest as they are transmitted by both food and water sources. In addition to being human pathogens, microsporidiosis has major economic impacts on agriculture (via effects on insects and sericulture), aquaculture and animals (food, domestic and wildlife). Microsporidia produce spores with a unique invasion mechanism, the polar tube, that is one of the most complex single celled forms known in the biological world. The mechanism by which the polar tube interacts with the host cell during invasion is still unknown. A long standing research program in my laboratory group is focused on understanding the mechanism of invasion and the structural biology and composition of the polar tube. We have developed techniques for the purificaiton of this structure, identified polar tube proteins (PTPs) and their post translational modifications and how these proteins interact. Futhermore, our studies have begun to define the functional roles of these proteins in the structural biology of the polar tube and the process of invasion. However, the full complement of proteins in this structure and the interactions of these components during invasion remain to be determined, In other microbes studies on invasion have provided key data for understanding pathogenesis and for new therapeutic approaches to the management of infections. We have demonstrated that the major polar tube protein is O-manosylated, a post translational modification that is involved in invasion, that inhibiting binding of manose can limit infection, and that antibody to polar tube protein 1 (PTP1) can block invasion demonstrate that targeting the invasion organelle is a way to limit infection. The proposed research project will employ a combination of proteomic, immunologic and ultrastructural studies to characterize the polar tube and its protein interactome to better define and study the mechanism of invasion. We will also evaluate the ability of a newly identified polar tube protein (PTP4) to bind to host cell components and use antibody to PTP4 as a marker to identify the area of the cell at which invasion is occurring. This will facilitate a detailed correlated microscopic analysis of the mechanism of invasion by these pathogens. Furthermore, electron microscopic techniques will be employed to provide insight into the three dimenstional structure of the proteins making up the polar tube providng critical information on fundamental questions concerning the organization of this invasion organelle that have not been able to be resolved by traditional microscopy. Studies of the composition, formation and function of this organelle during germination and invasion should provide a basis for the development of new strategies for control of these important parasitic protists.

摘要微孢子虫是一种与真菌相关的重要寄生虫，研究较多。 超过150年。他们在利用所有动物方面都很出色，从神秘的，良性的 感染壮观的、大规模的感染，造成广泛的损害，通常是宿主的死亡。 微孢子虫是艾滋病患者最常见的引起腹泻的机会性病原体， 脑炎、肌炎或结膜炎。微孢子虫也可以引起其他免疫系统的感染。 受感染的宿主，如接受过器官移植或免疫的患者 调整疗法。它们也能够感染免疫能力强的宿主，最常见的是引起 角结膜炎或腹泻。这些病原体被归类为NIH B类优先 病原体和环保局感兴趣的病原体，因为它们是通过食物和水源传播的。在……里面 除了是人类病原体外，微孢子虫病还对农业有重大的经济影响(通过影响 (昆虫和蚕业)、水产养殖和动物(食用、家养和野生动物)。微孢子虫产生物 孢子具有独特的入侵机制，即极管，这是最复杂的单细胞之一 生物界已知的形式。极管与宿主细胞相互作用的机制 入侵的时间还不得而知。我的实验室小组的一个长期研究项目专注于 了解入侵机制以及极管的结构生物学和组成。我们 已经开发出纯化这种结构的技术，鉴定了极管蛋白(PTP)和 它们的翻译后修饰以及这些蛋白质如何相互作用。此外，我们的研究已经开始 为了确定这些蛋白质在极管结构生物学和过程中的功能作用 入侵。然而，这种结构中的全部蛋白质以及这些蛋白质之间的相互作用 入侵过程中的成分仍有待确定，在其他微生物中，关于入侵的研究已经提供 为了解发病机制和管理新的治疗方法提供关键数据 感染。我们已经证明了主要的极管蛋白是O-甘露糖化的，这是一种翻译后 参与入侵的修饰，抑制甘露糖的结合可以限制感染，以及 抗极管蛋白1抗体可阻断侵袭证明靶向侵袭细胞器 是一种限制感染的方法。拟议的研究项目将采用蛋白质组学、 免疫学和超微结构研究极管及其蛋白相互作用组的特征 定义和研究入侵机制。我们还将评估一个新发现的极地的能力 管蛋白(PTP4)与宿主细胞成分结合，并以PTP4抗体为标志识别 发生入侵的细胞区域。这将有助于进行详细的相关显微分析 这些病原体入侵的机制。此外，电子显微镜技术将被 用来洞察组成极管的蛋白质的三维结构 提供有关入侵细胞器组织的基本问题的关键信息 这是传统显微镜无法分辨的。关于它的组成、形成和发展的研究 这种细胞器在萌发和入侵过程中的功能应为其发育提供基础 控制这些重要寄生原生生物的新策略。