Characterization of the Brucella virB locus
布鲁氏菌 virB 基因座的表征
基本信息
- 批准号:7736032
- 负责人:
- 金额:$ 33.65万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-07-01 至 2011-08-31
- 项目状态:已结题
- 来源:
- 关键词:AreaAutomobile DrivingBacteriaBrucellaBrucella abortusBrucellosisCattleCellsDevelopmentDiagnosticDiseaseEndoplasmic ReticulumEnvironmentFeverGoalsGoatHealthHumanImmuneImmune responseInfectionMediatingMethodsMilkMolecularMorbidity - disease rateMusPathogenesisPatternPhagocytesProteinsResearchReticuloendothelial SystemRoleSheepTestingTextTimeTissuesType IV Secretion System PathwayVaccinesVacuoleVirulenceVirulence FactorsWorkabstractingbaseimprovedmicrobialpathogen
项目摘要
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vii
longer than 30 lines of text.
Human brucellosis, caused by Bruce/Ia spp., is one of the most widespread zoonotic diseases globally, with an estimated 500,000 new cases each year. An
important aspect of B. abortus infection is its ability to persist within phagocytic cells of the reticuloendothelial system. We have shown that the virB locus, encoding a Type IV secretion system (T4SS), is essential for survival in phagocytes and virulence in mice. However, the mechanisms by which the T4SS allows B. abortus to establish its niche in the host are unknown. The objective of this application is to characterize the role of molecules secreted by the B. abortus T4SS in interaction with host cells. The central hypothesis of this application is that the T4SS functions in establishing a replicative niche in the host by
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targeting the Bruce//a-containing vacuole to the endoplasmic reticulum (ER). The rationale for the proposed research is that characterization of virulence mechanisms
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excellent research environment that is highly conducive to its successful completion. The central hypothesis will be tested and the objectives of this application accomplished by pursuing the following specific aim: (i) Determine the contribution of T4SS-translocated effector proteins to persistent infection of the reticuloendothelial system
significantly influencing concepts and methods driving the field.
在这里输入文本,即应用程序的新抽象信息。这部分必须是no
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Renee M Tsolis其他文献
Renee M Tsolis的其他文献
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{{ truncateString('Renee M Tsolis', 18)}}的其他基金
2023 Salmonella Biology and Pathogenesis Gordon Research Conference and Seminar
2023年沙门氏菌生物学与发病机制戈登研究会议暨研讨会
- 批准号:
10683617 - 财政年份:2023
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10468025 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10224776 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10022095 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
2019 Microbial Adhesion and Signal Transduction GRC/GRS
2019微生物粘附与信号转导GRC/GRS
- 批准号:
9752745 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10683118 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10772361 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Neutrophil-intrinsic role of SLC11A1/NRAMP1 in control of bacterial infection
SLC11A1/NRAMP1 在控制细菌感染中的中性粒细胞内在作用
- 批准号:
10755395 - 财政年份:2019
- 资助金额:
$ 33.65万 - 项目类别:
Systemic infections with non-typhoidal Salmonella
非伤寒沙门氏菌全身感染
- 批准号:
9238432 - 财政年份:2016
- 资助金额:
$ 33.65万 - 项目类别:
Detection of bacterial Type IV secretion by the unfolded protein response
通过未折叠蛋白反应检测细菌 IV 型分泌物
- 批准号:
8718850 - 财政年份:2014
- 资助金额:
$ 33.65万 - 项目类别:
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