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Cell-Binding Adhesins of Leptospira interrogans

Cell-Binding Adhesins of Leptospira interrogans
问号钩端螺旋体的细胞结合粘附素
批准号:
8265031
负责人:
Jenifer L Coburn
金额:
$19.13万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-01 至 2014-02-28

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英文摘要
DESCRIPTION (provided by applicant): On a worldwide basis, leptospirosis is the most widespread zoonotic disease. Leptospirosis is also emerging as a significant infectious disease in urban slums, particularly in tropical regions. The infection is caused by spirochetes of the genus Leptospira, and varies in severity from mild illness to fatal hemorrhagic disease with multiple organ failure. Disease severity varies with the host species, host age and health status, and the infecting strain. Virtually all species of mammals can serve as carriers, with the Leptospira persisting in the proximal tubules of the kidney and being shed in the urine. The persistence of leptospirosis in wildlife, companion animals, livestock, and in particular peridomestic rats, results in a continuous reservoir for human infection through exposure to animal tissue or body fluids containing Leptospira, or to urine-contaminated water sources. The bacteria enter through mucous membranes or skin abrasions, then disseminate to multiple tissues and can establish persistent infection in particular sites, most importantly the proximal tubules of the kidney. In addition, widespread endothelial damage is a feature of leptospirosis. Adhesion to host cell surfaces and extracellular matrix (ECM) is critical to the pathogenesis of disease for many pathogens. This is likely to be true of Leptospira, as well, but previous investigations into adhesion of Leptospira to mammalian tissue components have focused on interactions with the ECM. This proposal will follow up on our recent findings that the bacteria bind more efficiently to the cell surface than to the ECM, and that attachment to endothelial cells triggers disruption of cell layer integrity but does not kill the cells. These results suggest the presence of additional, significant, unexplored aspects of the interactions of pathogenic leptospires with the host. The goal of this project is to employ several complementary approaches to identify Leptospira interrogans molecules involved specifically in attachment to human cell surface receptors and altering the biology of host cells. The long-term goal of this line of work is to better understand the nature and consequences of Leptospira interactions with mammalian cells, which may eventually be useful in future development of improved vaccines or therapeutic approaches. PUBLIC HEALTH RELEVANCE: Leptospirosis is a potentially fatal infectious disease with global distribution. The higher prevalence of leptospirosis in the developing world suggests that preventive measures, such as vaccines that are effective against diverse Leptospira strains, would have a significant impact on human and animal health. As a step toward development of improved vaccines, we will identify and establish the significance of leptospiral molecules required for the bacteria to cause infection and disease manifestations.
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Invasion Dynamics
Genetic Approaches to Evaluation of the Roles of Leptospira interrogans Adhesins in Endothelial Interactions
  • 批准号:
    10389686
  • 项目类别:
  • 资助金额:
    $23.4万
  • 财政年份:
    2022
  • 负责人:
    Jenifer L Coburn
  • 依托单位:
Genetic Approaches to Evaluation of the Roles of Leptospira interrogans Adhesins in Endothelial Interactions
  • 批准号:
    10612825
  • 项目类别:
  • 资助金额:
    $19.5万
  • 财政年份:
    2022
  • 负责人:
    Jenifer L Coburn
  • 依托单位:
Mechanisms of Leptospira interrogans interactions with the vascular endothelium in vivo
  • 批准号:
    10208696
  • 项目类别:
  • 资助金额:
    $23.7万
  • 财政年份:
    2020
  • 负责人:
    Jenifer L Coburn
  • 依托单位:
海外基金