Roles for motility in Helicobacter pylori pathogenesis
Roles for motility in Helicobacter pylori pathogenesis
批准号:
8076315
负责人:
Karen M Ottemann
金额:
$35.05万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2013-05-31
关键词:
AffectAmino AcidsAnimalsAnti-Bacterial AgentsAntibioticsAntralBacillus subtilisBacteriaBindingBiochemical GeneticsBiochemical ReactionBiologyCarcinogensCellsChemicalsChemoreceptorsChemotaxisChronicClinicalComplexComprehensionCuesCysteineDataDiseaseEnvironmentEpitheliumEscherichia coliExtracellular StructureFlagellaGastric AdenocarcinomaGastric mucosaGastric ulcerGastritisGenetic TechniquesGoalsGrowthHelicobacter InfectionsHelicobacter pyloriHistidineHomologous GeneHumanImmuneInfectionInflammationInflammatory ResponseInternational Agency for Research on CancerIronLocationMetalsMethodsMicrobeMolecularNatureNutrientOrganismPathogenesisPhosphoric Monoester HydrolasesPlayPopulationProcessPropertyProtein DephosphorylationProteinsRelative (related person)RestRisk FactorsRoleRotationSet proteinSignal TransductionSiteStomachSwimmingSymptomsSystemTestingTherapeuticUlcerVaccinesVariantWorkWorld Health Organizationbasecell motilitycofactordesignexpectationinterestmalignant stomach neoplasmmicroorganismmucosa-associated lymphoid tissue lymphomamutantpathogenresearch studyresponse
中文摘要
描述(由申请人提供):幽门螺杆菌是一种人类胃病原体,感染了世界上大约一半的人口,引起从无症状胃炎到胃溃疡到胃癌的各种疾病。保守估计表明,5%的感染者(1.5亿人)患上某种形式的疾病。幽门螺杆菌是唯一一种被世界卫生组织国际癌症研究机构列为I类致癌物的细菌。这种细菌感染是几种类型胃癌的危险因素,包括胃腺癌和粘膜相关淋巴组织(MALT)淋巴瘤。幽门螺旋杆菌有几种能力帮助它定植并引起疾病。这些能力之一是定向运动性,或趋化性。趋化性是生物体感知环境并作出反应的能力。我们发现趋化性有助于幽门螺杆菌感染。特别是,我们发现趋化性有助于幽门螺杆菌最初建立感染,维持慢性感染,在胃的所有区域定植,并引起疾病的第一步,炎症。我们感兴趣的是更好地了解趋化性如何帮助幽门螺杆菌感染。为了实现这一目标,我们提出了三个目标:(1)确定趋化性如何促进胃窦定植以及趋化性如何引发炎症;(2)确定幽门螺杆菌如何利用趋化作用向一种关键的营养物质铁移动;(3)剖析信息是如何从感知环境的趋化受体传递到趋化信号转导级联的。特别是,确定CheZ和三个chev的角色。微生物对抗生素的耐药性越来越强,因此我们需要更清楚地了解感染机制。因此,这些实验可以帮助我们确定关键的抗生素或疫苗目标。摘要:幽门螺杆菌是一种感染人类胃的微生物,感染了世界上大约一半的人口,引起从无症状胃炎到胃溃疡再到胃癌的各种疾病。帮助幽门螺旋杆菌在胃里存活的细菌的一个特性是它的游泳能力。我们的工作旨在确定幽门螺杆菌游泳是如何促进疾病并帮助细菌寻找营养的。此外,我们将剖析这一过程的分子细节,以确定蛋白质,将成为良好的抗菌目标的长期目标。
英文摘要
DESCRIPTION (provided by applicant): Helicobacter pylori is a human gastric pathogen that infects approximately half of the world's population, causing diseases that range from asymptomatic gastritis to gastric ulcers to gastric cancers. Conservative estimates suggest that 5% of those infected-150 million people-develop some form of disease. H. pylori has the dubious distinction of being the only bacterium classified as a Group I carcinogen by the International Agency for Research on Cancer of the World Health Organization. Infection by this bacterium is a risk factor for several types of gastric cancer including gastric adenocarcinoma and mucosa-associated lymphoid tissue (MALT) lymphoma. H. pylori possesses several abilities that help it colonize and cause disease. One of these abilities is directed motility, or chemotaxis. Chemotaxis is the ability of an organism to sense its environment and move in response. We have found that chemotaxis aids H. pylori infection. In particular, we have found that chemotaxis helps the H. pylori establish infection initially, maintain a chronic infection, colonize all regions of the stomach and cause the first step of disease, inflammation. We are interested in a better understanding of how chemotaxis helps H. pylori infect. Toward this goal we propose three aims: (1) Determine how chemotaxis promotes colonization of the stomach antrum and how chemotaxis triggers inflammation; (2) Ascertain how H. pylori uses chemotaxis to move towards a critical nutrient, iron; (3) Dissect how information is relayed from the chemoreceptors, which sense the environment, to the chemotaxis signal transduction cascade. In particular, determine the roles of CheZ and the three CheVs. Microbes increasingly resist antibiotics, so we need a clearer comprehension of infectious mechanisms. Thus these experiments may help us pinpoint key antibiotic or vaccine targets. Lay Summary: Helicobacter pylori is a human stomach-infecting microbe that infects approximately half of the world's population, causing diseases that range from asymptomatic gastritis to gastric ulcers to gastric cancers. One bacterial property that helps H. pylori survive in the stomach is the ability to swim. Our work aims to determine how H. pylori swimming promotes disease and helps the bacterium find nutrients. Additionally, we will dissect the molecular details of this process, with the long-term goal of identifying proteins that would make good antibacterial targets.
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DOI:
10.1146/annurev-micro-090110-102908
发表时间:
2011
期刊:
Annual review of microbiology
影响因子:
10.5
作者:
[Lertsethtakarn P, Ottemann KM, Hendrixson DR]
通讯作者:
Hendrixson DR
DOI:
10.1099/mic.0.021857-0
发表时间:
2009-04
期刊:
Microbiology (Reading, England)
影响因子:
--
作者:
[Lowenthal AC, Simon C, Fair AS, Mehmood K, Terry K, Anastasia S, Ottemann KM]
通讯作者:
Ottemann KM
DOI:
10.1099/mic.0.062877-0
发表时间:
2013
期刊:
Microbiology
影响因子:
1.5
作者:
[L. Sanders;T. Andermann;K. Ottemann]
通讯作者:
L. Sanders;T. Andermann;K. Ottemann
DOI:
10.1186/1756-0500-3-77
发表时间:
2010-03-16
期刊:
BMC research notes
影响因子:
1.8
作者:
[Li J, Go AC, Ward MJ, Ottemann KM]
通讯作者:
Ottemann KM
DOI:
10.1111/j.1365-2958.2010.07200.x
发表时间:
2010-07-01
期刊:
Molecular microbiology
影响因子:
3.6
作者:
[Lertsethtakarn P, Ottemann KM]
通讯作者:
Ottemann KM
共 6 条
2022 Sensory Transduction in Microorganisms GRC & GRS
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批准号:10374971
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项目类别:
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资助金额:$0.8万
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财政年份:2021
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依托单位:
Understanding and manipulating chronic Helicobacter pylori to enhance treatment
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批准号:10641872
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资助金额:$37.76万
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财政年份:2021
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Understanding and manipulating chronic Helicobacter pylori to enhance treatment
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批准号:10316849
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资助金额:$37.76万
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财政年份:2021
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Understanding and manipulating chronic Helicobacter pylori to enhance treatment
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批准号:10452625
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资助金额:$37.76万
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财政年份:2021
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依托单位:
The function of chemotactic signal transduction during colonization and disease
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批准号:10490867
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资助金额:$42.77万
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财政年份:2015
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依托单位:
The function of chemotactic signal transduction during colonization and disease
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批准号:9793029
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资助金额:$4.36万
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The function of chemotactic signal transduction during colonization and disease
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批准号:9793025
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资助金额:$3.61万
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依托单位:
The function of chemotactic signal transduction during colonization and disease
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批准号:10389094
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资助金额:$43.95万
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财政年份:2015
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负责人:Karen M Ottemann
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依托单位:
The function of chemotactic signal transduction during colonization and disease
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批准号:10686164
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资助金额:$43.0万
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财政年份:2015
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负责人:Karen M Ottemann
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依托单位:
An anti-inflammatory protein of H. pylori: mechanism and diagnostic potential
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批准号:8582512
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项目类别:
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资助金额:$17.05万
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财政年份:2013
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负责人:Karen M Ottemann
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依托单位:
Roles for Motility in Helicobactor pylori pathogenesis
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批准号:6943805
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项目类别:
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资助金额:$4.77万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
NCRR: Purchase of Zeiss LSM5 Pascal Confocal Microscope
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批准号:6730878
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项目类别:
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资助金额:$25.81万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
PASCAL CONFOCAL MICROSCOPE: IMMUNOLOGYINFECTIOUS DIS: VIBIO CHOLERAE, HELICOBACT
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批准号:6973719
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项目类别:
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资助金额:$13.94万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
PASCAL CONFOCAL MICROSCOPE: VISUAL CONNECTION IN VIVO
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项目类别:
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资助金额:$4.65万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
PASCAL CONFOCAL MICROSCOPE: ENVIRONMENTAL TOXIC: LEAD, COPPER
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批准号:6973721
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项目类别:
-
资助金额:$2.58万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
PASCAL CONFOCAL MICROSCOPE: NEUROSCIENCE, PARKINSON'S DISEASE
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批准号:6973718
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项目类别:
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资助金额:$4.65万
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财政年份:2004
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负责人:Karen M Ottemann
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依托单位:
Roles for Motility in Helicobactor pylori pathogenesis
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批准号:7039090
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项目类别:
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资助金额:$34.08万
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财政年份:2002
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负责人:Karen M Ottemann
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依托单位:
Roles for motility in Helicobacter pylori pathogenesis
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批准号:7866661
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项目类别:
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资助金额:$35.53万
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财政年份:2002
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负责人:Karen M Ottemann
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依托单位:
Roles for Motility in Helicobactor pylori pathogenesis
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批准号:6865420
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项目类别:
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资助金额:$42.83万
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财政年份:2002
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负责人:Karen M Ottemann
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依托单位:
Roles for Motility in Helicobactor pylori pathogenesis
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批准号:6718969
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项目类别:
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资助金额:$29.8万
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财政年份:2002
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负责人:Karen M Ottemann
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依托单位:
海外基金