The interaction of Chlamydia with the host cytoskeleton

衣原体与宿主细胞骨架的相互作用

基本信息

批准号：
8289600
负责人：
SCOTT S GRIESHABER
金额：
$ 35.9万
依托单位：
UNIVERSITY OF FLORIDA
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-07-01 至 2014-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8289600
关键词：
Antibodies Bacteria Binding Biochemical Biological Assay Blindness Cell division Cells Centrosome Chimeric Proteins Chlamydia Chlamydia Infections Chlamydia trachomatis Chromosomal Instability Chromosomes Coculture Techniques Color Complex Cytokinesis Cytoskeleton DNA Defect Density Gradient Centrifugation Development Dynein ATPase Escherichia coli Expression Library Failure Fluorescent Dyes Genital system Goals Growth Health Hour Human Human Papillomavirus Human papilloma virus infection Human papillomavirus 16 Image Imagery Immune Sera Immunoprecipitation In Vitro Incidence Infection Infertility Label Lead Libraries Life Life Cycle Stages Link Maintenance Malignant Neoplasms Malignant neoplasm of cervix uteri Mass Spectrum Analysis Mediating Membrane Microscopy Microtubule Polymerization Microtubule-Associated Proteins Microtubule-Organizing Center Microtubules Monoclonal Antibodies Motor Mus Oncogenes Organelles Organism Outcome Pathogenesis Patients Pelvic Inflammatory Disease Play Process Protein Binding Protein Biosynthesis Protein Fragment Proteins Reporting Research Role Scheme System Techniques Tertiary Protein Structure Time Trimethoprim-Sulfamethoxazole United States Vacuole Woman adapter protein animal tissue base cellular imaging cofactor cross reactivity daughter cell extracellular genetic regulatory protein high risk inhibitor/antagonist metaplastic cell transformation migration mouse development new therapeutic target pathogen protein complex segregation trafficking uptake

项目摘要

DESCRIPTION (provided by applicant): The obligate intracellular bacterium Chlamydia trachomatis is the world's leading cause of preventable blindness and the most common sexually transmitted bacterial pathogen of humans. In the US, the incidence of new cases of chlamydial genital tract infection is approximately 4 million annually, causing severe illness such as pelvic inflammatory disease leading to tubal infertility. Chlamydia replication takes place in a unique membrane bound compartment within the host cell termed the inclusion. One of the earliest steps in inclusion maturation is centripetal migration to the perinuclear region, a process that is conserved among all chlamydial species suggesting an important role in pathogenesis. This migration is chlamydial driven, as chlamydial protein synthesis is required for the recruitment of the microtubule motor protein dynein. Dynein recruitment and activation is required for chlamydial inclusion trafficking to the microtubule organizing center (MTOC) of the cell, which ultimately leads to an intimate association between the inclusion and the host centrosome. The mature chlamydial inclusion remains associated with the centrosomes causing centrosome number defects, spindle defects, and chromosome instability. We hypothesize that the recruitment and activation of dynein is a central mechanism of pathogenesis during chlamydial infection. The focus of this proposal is to identify the chlamydial proteins involved in dynein activation, and investigate the role of dynein and centrosomes in cell to cell spread and cellular transformation. Aim 1 will identify chlamydial proteins that bind to dynein using dynein immunoprecipitation, centrosome purification and microtubule isolation techniques. Centrosomes are dynamic organelles and are actively partitioned into daughter cells during cell division, therefore Aim 2 will investigate the role of dynein and the centrosome in cell-to-cell spread of Chlamydia under persistent and non-persistent growth conditions. Centrosome function is crucial in the maintenance of chromosome fidelity. The unique chlamydial driven interaction between dynein and the inclusion is likely an important factor in the link between chlamydial infection and cervical cancer. Aim 3 will determine the mechanism of chlamydial induced centrosome defects and evaluate these defects in cellular transformation. Additionally, the link between cervical cancer and Chlamydia likely involves an interaction with human papilloma virus (HPV) infection. We will therefore assess the role of the interaction between chlamydial induced centrosome defects and expression of the high risk HPV16 E6 and E7 oncogenes on cellular transformation. PUBLIC HEALTH RELEVANCE: The bacteria Chlamydia infects an estimated 4 million people annually in the United States. Infection with this organism leads to pelvic inflammatory disease, infertility in women and raises the chance of cervical cancer development. Determining the mechanisms of chlamydial intracellular development and its impact on host cell replication machinery will lead to advances in understanding chlamydial disease and offer potential novel therapeutic targets.

描述（由申请人提供）：专性细胞内细菌沙眼衣原体是世界上可预防性失明的主要原因，也是人类最常见的性传播细菌病原体。在美国，衣原体生殖道感染每年新发病例约为400万例，引起盆腔炎等严重疾病，导致输卵管性不孕。衣原体复制发生在宿主细胞内独特的膜结合区室中，称为包涵体。包涵体成熟的最早步骤之一是向核周区域的向心迁移，这一过程在所有衣原体物种中都是保守的，表明在发病机制中发挥着重要作用。这种迁移是衣原体驱动的，因为招募微管运动蛋白动力蛋白需要衣原体蛋白合成。衣原体包涵体运输到细胞的微管组织中心（MTOC）需要动力蛋白的招募和激活，最终导致包涵体与宿主中心体之间的密切联系。成熟的衣原体包涵体仍然与中心体相关，导致中心体数量缺陷、纺锤体缺陷和染色体不稳定。我们假设动力蛋白的募集和激活是衣原体感染期间发病机制的核心机制。该提案的重点是鉴定参与动力蛋白激活的衣原体蛋白，并研究动力蛋白和中心体在细胞间传播和细胞转化中的作用。目标 1 将使用动力蛋白免疫沉淀、中心体纯化和微管分离技术鉴定与动力蛋白结合的衣原体蛋白。中心体是动态细胞器，在细胞分裂过程中主动分裂成子细胞，因此 Aim 2 将研究动力蛋白和中心体在持续和非持续生长条件下衣原体细胞间传播中的作用。中心体功能对于维持染色体保真度至关重要。动力蛋白和包涵体之间独特的衣原体驱动的相互作用可能是衣原体感染与宫颈癌之间联系的重要因素。目标 3 将确定衣原体诱导中心体缺陷的机制并评估细胞转化中的这些缺陷。此外，宫颈癌和衣原体之间的联系可能涉及与人乳头瘤病毒（HPV）感染的相互作用。因此，我们将评估衣原体诱导的中心体缺陷与高危 HPV16 E6 和 E7 癌基因表达之间的相互作用对细胞转化的作用。公共卫生相关性：在美国，衣原体细菌每年感染约 400 万人。感染这种微生物会导致盆腔炎、女性不孕，并增加患宫颈癌的机会。确定衣原体细胞内发育的机制及其对宿主细胞复制机制的影响将促进对衣原体疾病的理解并提供潜在的新治疗靶点。