Severe Enteric Disease: Pathogenesis and Response

严重肠道疾病：发病机制和反应

• 批准号: 8292147
• 负责人: JAMES B KAPER
• 金额: $ 140.95万
• 依托单位: UNIVERSITY OF MARYLAND BALTIMORE
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-20 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8292147
• 关键词: Address; Adult; Age; Antigens; Area; Asia; Bacteria; Bacterial Infections; Biological Assay; Biological Markers; Biometry; Cessation of life; Child; Childhood; Clinical; Clinical Research; Clostridium; Collaborations; Communicable Diseases; Country; DNA; Data; Databases; Diarrhea; Disease; Doctor of Philosophy; Dysentery; Enteral; Enterobacteriaceae; Enterococcus; Enterotoxins; Epidemiologic Studies; Epidemiology; Epithelial; Epithelial Cells; Escherichia coli; Escherichia coli EHEC; Escherichia coli Infections; Event; Faculty; Feces; Freezing; Functional disorder; Gastroenterologist; Gastrointestinal tract structure; Genes; Genetic; Genome; Genomics; Genotype; Goals; Health; Human; Human Genetics; Human Microbiome; IL8 gene; Immune response; Immune system; Immunoglobulin A; Immunoglobulin G; Immunoglobulins; Immunology; In Vitro; Individual; Infection; Infection Control; Inflammation; Inflammatory; Interleukin-10; International; Intestinal Motility; Intestines; Investigation; Knockout Mice; Laboratories; Lactobacillus; Lactoferrin; Leadership; Maryland; Metagenomics; Modeling; Multicenter Studies; Mus; Nucleic Acids; Outcome; Pathogenesis; Pathogenicity Island; Patients; Pattern recognition receptor; Permeability; Physiological; Physiology; Polymorphism Analysis; Predisposition; Production; Recording of previous events; Research; Research Personnel; Research Project Grants; Resources; Role; Scientist; Sequence Analysis; Series; Serine Protease; Shigella; Shigella Infections; Single Nucleotide Polymorphism; Site; South Africa; Specialist; Specimen; Strategic Planning; Symptoms; TLR4 gene; Testing; Tissues; Tumor necrosis factor receptor 11b; Type III Secretion System Pathway; Universities; Ursidae Family; Veillonella; Virulence; Virulence Factors; Work; adaptive immunity; authority; cytokine; enteric pathogen; enteroaggregative Escherichia coli; enteropathogenic Escherichia coli; enterotoxigenic Escherichia coli; genome sequencing; in vitro Assay; insight; intestinal epithelium; mast cell; member; microbial; microbiome; multidisciplinary; mutant; pathogen; public health relevance; research study; response; vaccine evaluation; volunteer

DESCRIPTION (provided by applicant): Infectious enteric diseases are major health problem throughout the world. This application seeks to establish the University of Maryland Enterics Research Investigational Network (ERIN) Cooperative Research Center (CRC) to investigate important clinical, pathogenesis, and host response Issues of enteric disease. The particular enteric pathogens that will be the focus of this CRC are Shigella spp. and diarrheagenic E. coli (DEC), which were implicated as the bacterial pathogens most frequently isolated from fatal cases of diarrheal disease in the Global Enteric Multicenter Study (GEMS). The GEMS is being conducted at 7 sites in Africa and South Asia and is the largest study ever conducted of diarrheal disease in children under the age of 5. Clinical specimens and bacterial isolates from GEMS as well as hypotheses arising from this study will be further examined using a variety of approaches including bacterial pathogenesis assays, intestinal physiology studies, fecal adaptive immunity and immunological markers, bacterial genomics, microbiomes, and human SNP analysis. Three multi-component and highly integrated projects are proposed. Project 1 will focus on the pathogenesis of DEC and Shigella infections. Genome sequences of enteropathogenic E. coli (EPEC) strains isolated from lethal cases of diarrhea, from non-lethal infections and from controls will be determined. Potential EPEC virulence factors implicated in the genomic analysis will be further characterized using a variety of assays and models to study pathogenesis. An enterotoxin originally discovered in Shigella but also present in DEC will be further characterized. In Project 2, different aspects of host response will be studied, including physiology studies of intestinal tissue infected with wild type and mutant Shigella and DEC strains, as well as the characterization of fecal immunoglobulin and cytokine levels in stool specimens from GEMS patients. Project 3 will investigate clinical aspects using clinical specimens from GEMS to determine patient SNPs in genes previously associated with susceptibility to diarrheal disease, bacterial interactions using microbiome and laboratory co-infection studies, and studies on the pangenomics of Shigella strains isolated from lethal and non-lethal disease.

描述（由申请人提供）：传染性肠道疾病是世界范围内的主要健康问题。本申请旨在建立马里兰州大学肠道研究调查网络（ERIN）合作研究中心（CRC），以调查肠道疾病的重要临床、发病机制和宿主反应问题。本CRC重点关注的特定肠道病原体是志贺氏菌属。和嗜热E.大肠杆菌（DEC），其被认为是全球肠道多中心研究（GEMS）中最常从致死性腹泻病例中分离的细菌病原体。GEMS正在非洲和南亚的7个地点进行，是有史以来对5岁以下儿童腹泻病进行的最大规模的研究。将使用多种方法进一步检查GEMS的临床标本和细菌分离株以及本研究产生的假设，包括细菌致病性测定、肠道生理学研究、粪便适应性免疫和免疫学标记物、细菌基因组学、微生物组学和人类SNP分析。提出了三个多组成部分和高度综合的项目。项目1将侧重于DEC和志贺氏菌感染的发病机制。肠致病性E.将确定从致死性腹泻病例、非致死性感染和对照中分离的大肠杆菌（EPEC）菌株。基因组分析中涉及的潜在EPEC毒力因子将使用各种检测和模型进一步表征，以研究发病机制。一种最初在志贺氏菌中发现但也存在于DEC中的肠毒素将进一步表征。在项目2中，将研究宿主反应的不同方面，包括野生型和突变型志贺氏菌和DEC菌株感染的肠组织的生理学研究，以及GEMS患者粪便标本中粪便免疫球蛋白和细胞因子水平的表征。项目3将使用GEMS的临床标本研究临床方面，以确定先前与肠道疾病易感性相关的基因中的患者SNP，使用微生物组和实验室共感染研究的细菌相互作用，以及对从致死性和非致死性疾病中分离的志贺氏菌菌株的泛基因组学的研究。