Interactions between histophilus somni (haemophilus somnus) and phagocytic cells

睡眠嗜组织杆菌(睡眠嗜血杆菌)与吞噬细胞之间的相互作用

基本信息

  • 批准号:
    3574-2008
  • 负责人:
  • 金额:
    $ 1.82万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2011
  • 资助国家:
    加拿大
  • 起止时间:
    2011-01-01 至 2012-12-31
  • 项目状态:
    已结题

项目摘要

Histophilus somni is a Gram negative pathogen of cattle capable of causing a variety of diseases, including infections of lung, heart, joints, brain and reproductive tract. The control of H. somni infection has been accomplished through both antibiotic treatment as well as vaccination. However, given that the prevalence of this disease syndrome has been increasing over the past decade, improved control methods are clearly needed. Central to the ability of the organism to cause disease is its capability to evade host innate immune responses, the first line of defense against bacterial pathogens. Specifically, H. somni is able to suppress the antimicrobial activities of leukocytes, including PMNs and macrophages, resulting in enhanced survival of the organism and dissemination throughout the body. It is our hypothesis that H. somni produces specific proteins capable of modifying the host innate immune response, resulting in a general suppression. In order to test this hypothesis, we will characterize new proteins produced by the bacterium while it is incubated with bovine leukocytes using both functional genomic as well as traditional protein biochemistry techniques. These proteins will be fully characterized and the genes coding for each one isolated and used to construct mutant H. somni lacking each specific gene. These will then be tested for their ability to interfere with PMN function. Finally, we will test the ability of these mutants to cause disease in a bovine infection model. Ultimately, this will lead to the development of novel targets for both vaccine and therapeutic development.
索姆尼组织杆菌是一种革兰氏阴性病原体,可引起多种疾病,包括肺、心脏、关节、脑和生殖道感染。通过抗生素治疗和接种疫苗实现了对索姆尼嗜血杆菌感染的控制。然而,鉴于这种疾病综合征的流行率在过去十年中一直在增加,显然需要改进控制方法。生物体致病能力的核心是它逃避宿主先天免疫反应的能力,这是抵御细菌病原体的第一道防线。具体地说,H.Somni能够抑制包括PMN和巨噬细胞在内的白细胞的抗菌活性,从而提高生物的存活率并在全身传播。我们的假设是,H.Somni产生特定的蛋白质,能够修改宿主的先天性免疫反应,导致普遍的抑制。为了验证这一假设,我们将使用功能基因组和传统的蛋白质生物化学技术来表征细菌与牛白细胞孵育时产生的新蛋白质。这些蛋白质将被充分鉴定,每个蛋白质的编码基因将被分离出来,并用于构建缺失每个特定基因的突变索姆尼杆菌。然后将测试这些细胞干扰PMN功能的能力。最后,我们将在牛感染模型中测试这些突变体的致病能力。最终,这将导致疫苗和治疗开发的新靶点的开发。

项目成果

期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Potter, Andrew其他文献

Evaluating the efficiency performance of airports using an integrated AHP/DEA-AR technique
  • DOI:
    10.1016/j.tranpol.2015.04.008
  • 发表时间:
    2015-08-01
  • 期刊:
  • 影响因子:
    6.8
  • 作者:
    Lai, Po-Lin;Potter, Andrew;Beresford, Anthony
  • 通讯作者:
    Beresford, Anthony
Healthcare supply chain management in Malaysia: a case study
Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids.
  • DOI:
    10.1038/s41467-023-39420-6
  • 发表时间:
    2023-06-24
  • 期刊:
  • 影响因子:
    16.6
  • 作者:
    Sebastian, Rebecca;Jin, Kang;Pavon, Narciso;Bansal, Ruby;Potter, Andrew;Song, Yoonjae;Babu, Juliana;Gabriel, Rafael;Sun, Yubing;Aronow, Bruce;Pak, ChangHui
  • 通讯作者:
    Pak, ChangHui
Pin1 inhibitors: Pitfalls, progress and cellular pharmacology
Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution
  • DOI:
    10.1016/j.bmcl.2010.09.063
  • 发表时间:
    2010-11-15
  • 期刊:
  • 影响因子:
    2.7
  • 作者:
    Potter, Andrew;Oldfield, Victoria;Moore, Jonathan D.
  • 通讯作者:
    Moore, Jonathan D.

Potter, Andrew的其他文献

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{{ truncateString('Potter, Andrew', 18)}}的其他基金

Universality and topology in gapless systems and far from equilibrium
无间隙系统中的普遍性和拓扑结构且远离平衡
  • 批准号:
    RGPIN-2022-03585
  • 财政年份:
    2022
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Universality and topology in gapless systems and far from equilibrium
无间隙系统中的普遍性和拓扑结构且远离平衡
  • 批准号:
    DGECR-2022-00123
  • 财政年份:
    2022
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Launch Supplement
Interactions between histophilus somni (haemophilus somnus) and phagocytic cells
睡眠嗜组织杆菌(睡眠嗜血杆菌)与吞噬细胞之间的相互作用
  • 批准号:
    3574-2008
  • 财政年份:
    2012
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Interactions between histophilus somni (haemophilus somnus) and phagocytic cells
睡眠嗜组织杆菌(睡眠嗜血杆菌)与吞噬细胞之间的相互作用
  • 批准号:
    3574-2008
  • 财政年份:
    2010
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
NSERC/Bioniche Industrial Research Chair in Vaccines to Reduce Food and Water Contamination
NSERC/Bioniche 减少食品和水污染疫苗工业研究主席
  • 批准号:
    310009-2002
  • 财政年份:
    2009
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Industrial Research Chairs
Interactions between histophilus somni (haemophilus somnus) and phagocytic cells
睡眠嗜组织杆菌(睡眠嗜血杆菌)与吞噬细胞之间的相互作用
  • 批准号:
    3574-2008
  • 财政年份:
    2009
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Interactions between histophilus somni (haemophilus somnus) and phagocytic cells
睡眠嗜组织杆菌(睡眠嗜血杆菌)与吞噬细胞之间的相互作用
  • 批准号:
    3574-2008
  • 财政年份:
    2008
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Pan-PRovincial Vaccine ENTerprise
泛省疫苗企业
  • 批准号:
    363925-2007
  • 财政年份:
    2007
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Centres of Excellence for Commercialization and Research - Group
NSERC/Bioniche Industrial Research Chair in Vaccines to Reduce Food and Water Contamination
NSERC/Bioniche 减少食品和水污染疫苗工业研究主席
  • 批准号:
    310008-2002
  • 财政年份:
    2006
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Industrial Research Chairs
NSERC/Bioniche Chairs in vaccines to reduce food and water contamination
NSERC/Bioniche 主持减少食品和水污染的疫苗研究
  • 批准号:
    310008-2002
  • 财政年份:
    2005
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Industrial Research Chairs

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