Interaction of pathogenic Rhodococcus equi with mammalian macrophages
致病性马红球菌与哺乳动物巨噬细胞的相互作用
基本信息
- 批准号:5373507
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:德国
- 项目类别:Priority Programmes
- 财政年份:2002
- 资助国家:德国
- 起止时间:2001-12-31 至 2008-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
When microorganisms enter the sterile section of our body (e.g., after trauma), they readily encounter professional phagocytic cells (in particular, neutrophils and macrophages) which ingest and kill the microbes. Some intracellular pathogens, however, escape this host defense mechanism and can even multiply in phagocytic host cells. These microorganisms include members of the species Rhodococcus equi which are found in macrophage phagosomes that do not mature to phagolysosomes, and which can destroy their host cells in a matter of hours to days. These two unusual features are uniquely regulated by the presence of a plasmid which is essential for virulence of R. equi in mice and horses. The proposed studies will contribute to an understanding at the molecular level of how Rhodococcus-containing phagosomes are compartmentalized during an infection, how the bacteria can destroy their host cells and to what extent intracellular compartmentalization determines host cell destruction.
当微生物进入我们身体的无菌部分时(例如,在创伤后),它们容易遇到吞噬并杀死微生物的专职吞噬细胞(特别是嗜中性粒细胞和巨噬细胞)。然而,一些细胞内病原体逃避这种宿主防御机制,甚至可以在吞噬宿主细胞中繁殖。这些微生物包括马红球菌(Rhodococcus equi)物种的成员,马红球菌存在于不成熟为吞噬溶酶体的巨噬细胞吞噬体中,并且可以在数小时至数天内破坏其宿主细胞。这两个不寻常的特征是由一个质粒的存在,这是必不可少的毒力的R。在老鼠和马中的马。拟议的研究将有助于在分子水平上了解红球菌的吞噬体在感染过程中是如何划分的,细菌如何破坏宿主细胞,以及细胞内划分在多大程度上决定宿主细胞的破坏。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Professor Dr. Albert Haas其他文献
Professor Dr. Albert Haas的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Professor Dr. Albert Haas', 18)}}的其他基金
Priority Programme 1580: Administration, Workshops, Exchange Programme and Conferences
优先计划 1580:行政、研讨会、交流计划和会议
- 批准号:
199698457 - 财政年份:2011
- 资助金额:
-- - 项目类别:
Priority Programmes
Lysosomal Membrane Proteins and their Roles in Phagosome Maturation
溶酶体膜蛋白及其在吞噬体成熟中的作用
- 批准号:
198129374 - 财政年份:2011
- 资助金额:
-- - 项目类别:
Priority Programmes
Cell-free analysis of phagosome biogenesis in macrophages
巨噬细胞吞噬体生物发生的无细胞分析
- 批准号:
54760881 - 财政年份:2007
- 资助金额:
-- - 项目类别:
Research Grants
Molecular analysis of the biogenesis of Afipia-containing phagosomes in macrophages
巨噬细胞中含有 Afipia 的吞噬体生物发生的分子分析
- 批准号:
5353898 - 财政年份:2002
- 资助金额:
-- - 项目类别:
Research Grants
In vitro-Analyse der Phagosom-Lysosom-Fusion und ihrer Hemmung durch intrazelluläre Bakterien
吞噬体-溶酶体融合及其胞内细菌抑制的体外分析
- 批准号:
5301224 - 财政年份:1996
- 资助金额:
-- - 项目类别:
Research Grants
The Virulence-Associated Protein A (VapA) of Rhodococcus equi as a central manipulator of infected macrophages
马红球菌毒力相关蛋白 A (VapA) 作为受感染巨噬细胞的中央操纵者
- 批准号:
420695171 - 财政年份:
- 资助金额:
-- - 项目类别:
Research Grants
Phosphatidylinositol phosphates and their effector proteins in phagosome-lysosome tethering and fusion
磷脂酰肌醇磷酸盐及其在吞噬体-溶酶体束缚和融合中的效应蛋白
- 批准号:
414783339 - 财政年份:
- 资助金额:
-- - 项目类别:
Research Grants
相似国自然基金
Erk1/2/CREB/BDNF通路在CSF1R相关性白质脑病致病机制中的作用研究
- 批准号:82371255
- 批准年份:2023
- 资助金额:49.00 万元
- 项目类别:面上项目
CD8+T细胞亚群在抗MDA5抗体阳性皮肌炎中的致病机制研究
- 批准号:82371805
- 批准年份:2023
- 资助金额:45.00 万元
- 项目类别:面上项目
新生儿坏死性小肠结肠炎中去泛素化酶USP15调控ILC3分化损伤肠道粘膜屏障的致病机制研究
- 批准号:82371711
- 批准年份:2023
- 资助金额:49.00 万元
- 项目类别:面上项目
相似海外基金
Defining the cellular origin of pathogenic autoantibodies
定义致病性自身抗体的细胞起源
- 批准号:
EP/Y031091/1 - 财政年份:2024
- 资助金额:
-- - 项目类别:
Fellowship
Modelling to inform interventions during Highly Pathogenic Avian Influenza outbreaks in Great Britain
英国高致病性禽流感爆发期间的建模为干预措施提供信息
- 批准号:
BB/X016137/1 - 财政年份:2024
- 资助金额:
-- - 项目类别:
Research Grant
ECOFLU : Understanding the ecology of Highly Pathogenic Avian Influenza in wild bird populations
ECOFLU:了解野生鸟类中高致病性禽流感的生态学
- 批准号:
NE/Y001591/1 - 财政年份:2024
- 资助金额:
-- - 项目类别:
Research Grant
Oral pathogen - mediated pro-tumorigenic transformation through disruption of an Adherens Junction - associated RNAi machinery
通过破坏粘附连接相关的 RNAi 机制,口腔病原体介导促肿瘤转化
- 批准号:
10752248 - 财政年份:2024
- 资助金额:
-- - 项目类别:
Syudy on highly pathogenic avian influenza infection in innate immunity
Syudy 论高致病性禽流感感染的先天免疫
- 批准号:
23H02364 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Scientific Research (B)
Pathogenic role of senocules in synchronization of aging
senocules在衰老同步中的致病作用
- 批准号:
23H02911 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Scientific Research (B)
Elucidation of the pathogenic mechanism of de-differentiation into pancreatic adenocytes in diabetic pancreatic beta cells.
阐明糖尿病胰腺β细胞去分化为胰腺腺细胞的致病机制。
- 批准号:
23K07990 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Scientific Research (C)
Colonic mucus-derived sugars fuel the growth and virulence of pathogenic enteric bacteria.
结肠粘液衍生的糖促进致病性肠道细菌的生长和毒力。
- 批准号:
478324 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Operating Grants
Establishment of a comprehensive analysis platform for the microbiota, including pathogenic parasites and protozoan species, of archaeological soil materials.
建立考古土壤材料微生物群(包括病原寄生虫和原生动物种类)的综合分析平台。
- 批准号:
23K17518 - 财政年份:2023
- 资助金额:
-- - 项目类别:
Grant-in-Aid for Challenging Research (Exploratory)














{{item.name}}会员




