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Haemophilus Hap-mediated Microcolony Formation

Haemophilus Hap-mediated Microcolony Formation
嗜血杆菌 Hap 介导的微菌落形成
批准号:
6999862
负责人:
Joseph W. St. Geme
金额:
$26.32万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-01-01 至 2007-12-31

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英文摘要
DESCRIPTION (provided by applicant): Nontypable Haemophilus influenzae is a common cause of localized respiratory tract disease, including otitis media, sinusitis, bronchitis, and pneumonia. In addition, this organism causes serious systemic disease, such as meningitis, endocarditis, and septicemia. The initial step in the pathogenesis of nontypable H. influenzae disease involves colonization of the upper respiratory mucosa. We have identified an H. influenzae serine protease called Hap, which facilitates intimate interaction with epithelial cells and extracellular matrix proteins and also promotes bacterial aggregation and microcolony formation. Based on our in vitro results, we speculate that Hap plays an important role in the process of colonization. Hap belongs to the growing family of autotransporter proteins and is synthesized as a precursor protein with 3 functional domains, including an N-terminal signal sequence, an internal protease domain with adhesive activity (Haps), and a C-terminal outer membrane domain with translocator activity (HapBeta). Ultimately, Hap undergoes autoproteolytic cleavage, with extracellular release of Haps. In recent work, we demonstrated that Hap mediated adherence and microcolony formation are potentiated by a host protein called secretory leukocyteprotease inhibitor (SLPI). This protein is present in respiratory secretions and inhibits Hap autoproteolysis, resulting in accumulation of surface-associated Haps. In the present proposal, we will focus on Hap-mediated adherence and microcolony formation. In Aim 1, we will solve the crystal structure of Haps and define the interactive surfaces involved in adherence and microcolony formation. In Aim 2, we will examine the ability of microcolonies to resist killing by cationic peptides, to evade macrophage phagocytosis, and to enhance persistence in the chinchilla otitis media model. In Aim 3, we will characterize the relationship between respiratory viral infection and Hap-mediated adherence and microcolony formation, concentrating on the role of SLPI. From a practical perspective, the proposed studies may facilitate efforts to develop novel strategies forthe treatment and prevention of H. influenzae disease. Perhaps more importantly, they may provide general insights into host-microbe relationships and expand our understanding of microbial biofilms.
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Pathogenicity of the emerging pathogen Kingella kingae
  • 批准号:
    10559927
  • 项目类别:
  • 资助金额:
    $44.5万
  • 财政年份:
    2022
  • 负责人:
    Joseph W. St. Geme
  • 依托单位:
Molecular basis of virulence in the emerging pathogen Kingella kingae
  • 批准号:
    8731463
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    $39.36万
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    2013
  • 负责人:
    Joseph W. St. Geme
  • 依托单位:
Biology of the HMW1 and HMW2 Adhesins of H. Influenzae
  • 批准号:
    7850275
  • 项目类别:
  • 资助金额:
    $14.49万
  • 财政年份:
    2009
  • 负责人:
    Joseph W. St. Geme
  • 依托单位:
Center for Molecular & Cellular Studies of Ped Disease
  • 批准号:
    7994221
  • 项目类别:
  • 资助金额:
    $29.71万
  • 财政年份:
    2003
  • 负责人:
    Joseph W. St. Geme
  • 依托单位:
国内基金
海外基金
生物地球化学驱动的HAP原位反应带对酸法地浸采铀矿山退役采区地下水中铀的阻滞固定作用
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    2025
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基于PTEN敲除小鼠探索神经干细胞联合CS/Sr-HAP纳米复合生物工程支架促进SCI再生修复的应用研究
  • 批准号:
    LTGD23H090006
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    省市级项目
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  • 批准年份:
    2023
  • 负责人:
    解先宽
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水稻抗纹枯病优异等位基因OsERF86Hap1的抗病分子机制研究
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    面上项目
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    55万元
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    2022
  • 负责人:
    左示敏
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Hap1调控GR/CREB/BDNF信号通路影响AD小鼠认知功能的机制研究
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    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2022
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