Genetic Variation in genes involved in Neisseria gonorrhoeae LOS biosynthesis

淋病奈瑟菌 LOS 生物合成相关基因的遗传变异

• 批准号: 8210970
• 负责人: DANIEL C STEIN
• 金额: $ 22.05万
• 依托单位: UNIV OF MARYLAND, COLLEGE PARK
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-02-15 至 2014-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8210970
• 关键词: Address; Affect; Anabolism; Antigenic Variation; Bacteria; Biochemical; Biological; Biology; Blood; Cell surface; Cells; Clinical; Collaborations; Data; Disease; Ectopic Pregnancy; Engineering; Enzymes; Gene Cluster; Gene Structure; Genes; Genetic; Genetic Recombination; Genetic Variation; Genomics; Goals; Gonorrhea; HIV; Health; Health Care Costs; Human; Immune; Infection; Infection Control; Infertility; Invaded; Knowledge; Laboratories; Lead; Modeling; Modification; Molecular; Neisseria gonorrhoeae; Oligosaccharides; Organism; Outcome; Pathogenesis; Pathogenicity; Pelvic Inflammatory Disease; Phase; Play; Positioning Attribute; Prevention; Process; Property; Public Health; Research; Resistance; Role; Serum; Site; Stream; Structure; Surface Antigens; Synovial Fluid; Testing; United States; Vaccines; Variant; Virulence Factors; Woman; base; chronic pelvic pain; cost; design; human tissue; innovation; killings; lacto-N-neotetraose; lipooligosaccharide; novel; novel strategies; pathogen; prevent; tissue culture; tool; transmission process

DESCRIPTION (provided by applicant): Neisseria gonorrhoeae is responsible for over 1 million cases of gonorrhea each year in the United States. The total health care costs associated with treating gonorrhea, and complications that arise from infections caused by this organism exceed 1 billion dollars per year. Gonococcal infections can disseminate, from the initial site of infection causing pelvic inflammatory disease (PID), which can lead to tubal infertility, ectopic pregnancy, and chronic pelvic pain, or into the blood stream causing disseminated gonococcal infections (DGI). Lipooligosaccharide (LOS) is a prominent surface antigen and a virulence factor that makes a major contribution to the pathogenesis of these diseases. LOS can exist as multiple chemically related components on a single cell, with variations in the oligosaccharide portion readily interconverting between forms. While one form of this molecule has been extensively studied, there are many other novel structures that are known to exist. The fact that this pathogen possesses so many different ways to manipulate its LOS, and can make such a diversity of structures, indicates that such modifications are important in pathogenesis. The objective of this proposal is to determine the genetic variability associated with LOS biosynthesis and determine if specific LOS structures are associated with specific clinical outcomes of infection by defining the structures expressed by the gonococcus and characterizing the molecular and functional basis for the modulation of the expression of these structures. The central hypothesis of the proposed research is that variation in the biosynthesis of LOS has additional genetic and biochemical underpinnings that have yet to be characterized, and that they lead to the synthesis of additional LOS structures that contribute to different biological properties of the bacterium. I will characterize the structural variability that exists in this species and will use the genetic information obtained to construct strains with invariant defined LOS. I will then analyze the biological significance of these structures by determining their contribution to serum resistance. PUBLIC HEALTH RELEVANCE: rationale for wanting to know what LOS structures can be made in Neisseria gonorrhoeae, how changes in LOS structures occur and how such modulation affects the organism's pathogenicity is that, once this information becomes known, it will be possible to develop a comprehensive understanding of pathogenesis. This, in turn, is expected to lead to innovative new ways of preventing and controlling infection. I am well-positioned to undertake the proposed research because I have: developed the requisite genetic tools; cloned and characterized many of the currently known LO S biosynthetic genes; identified strains possessing alternative LOS structures; developed the requisite collaborations and adapted the appropriate tissue culture models to study the role of LOS in disease pathogenesis.

描述（由申请人提供）：淋病奈瑟菌在美国每年造成超过100万例淋病。与治疗淋病以及由该生物体引起的感染引起的并发症相关的总医疗保健费用每年超过10亿美元。淋球菌感染可以从感染的初始部位传播，引起盆腔炎性疾病（PID），这可能导致输卵管不孕症，异位妊娠和慢性盆腔疼痛，或进入血流引起播散性淋球菌感染（DGI）。脂寡糖（LOS）是一种重要的表面抗原和毒力因子，在这些疾病的发病机制中起着重要作用。LOS可以作为多种化学相关组分存在于单个细胞上，寡糖部分的变化容易在形式之间相互转化。虽然这种分子的一种形式已被广泛研究，但已知存在许多其他新结构。这种病原体具有如此多的不同方式来操纵其LOS，并且可以制造如此多样的结构，这一事实表明这种修饰在发病机制中是重要的。本提案的目的是确定与LOS生物合成相关的遗传变异性，并通过定义淋球菌表达的结构和表征这些结构表达调节的分子和功能基础，确定特定LOS结构是否与感染的特定临床结果相关。拟议研究的中心假设是，LOS生物合成的变化具有尚未表征的额外遗传和生化基础，并且它们导致合成额外的LOS结构，这些结构有助于细菌的不同生物学特性。我将描述该物种中存在的结构变异性，并将使用获得的遗传信息构建具有不变定义LOS的菌株。然后，我将通过确定它们对血清抵抗的贡献来分析这些结构的生物学意义。公共卫生相关性：想要知道淋病奈瑟菌中可以产生什么样的LOS结构、LOS结构的变化如何发生以及这种调节如何影响生物体的致病性的基本原理是，一旦这些信息被知道，就有可能对发病机理有全面的了解。这反过来又有望导致预防和控制感染的创新方法。我很好地定位进行拟议的研究，因为我已经：开发了必要的遗传工具;克隆和表征了许多目前已知的LOS生物合成基因;确定了具有替代LOS结构的菌株;开发了必要的合作和适应适当的组织培养模型，以研究LOS在疾病发病机制中的作用。