Novel Antimicrobials Targeting Bacterial Type IV Secretion Systems
Novel Antimicrobials Targeting Bacterial Type IV Secretion Systems
批准号:
8549945
负责人:
JAMES E KIRBY
金额:
$36.8万
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:
2012-09-24 至 2017-08-31
关键词:
Antibiotic ResistanceAntibioticsAreaBacteriaBacterial TypingBartonellaBartonella InfectionsBiological AssayBloodCellsCommunicable DiseasesCoxiella burnetiiDataDiseaseElementsExploratory/Developmental GrantExploratory/Developmental Grant for Diagnostic Cancer ImagingFutureGoalsGrowthHumanInfectionInjection of therapeutic agentLegionella pneumophilaLibrariesMaximum Tolerated DoseMetabolicModelingMusOrganismPharmaceutical ChemistryPharmaceutical PreparationsPharmacodynamicsPrevalenceRelative (related person)ResistanceSeriesSpecificityStructureStructure-Activity RelationshipSystemTestingTherapeuticTherapeutic AgentsTherapeutic EffectTissuesToxic effectType IV Secretion System PathwayVirulenceVirulence FactorsWorkanalogantimicrobialantimicrobial drugbasefollow-uphigh throughput screeningin vitro Assayin vivoin vivo Modelinhibitor/antagonistmacrophagenovelnovel therapeuticspathogenresearch studyresistance mechanismscaffoldscreeningsmall moleculetherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The increasing prevalence of antibiotic resistance is compromising our ability to treat infection. Therefore, this application's broad, long-term objective is to develop and establish proof of principle for a new class of therapeutics targeting pathogen host interaction. Many bacterial pathogens use specialized secretion systems to inject virulence factors into host cells. These systems are absolutely required for virulence and therefore offer a promising therapeutic target. The aim of this proposal is to establish type IV secretion systems (T4SS) -- one of the major classes of such injection apparatuses - as a target for antimicrobial therapy. We recently completed a high throughput screen of a 235,000 compound library using the model pathogen, Legionella pneumophila, in order to identify small molecule inhibitors of T4SS. Here, we propose to follow up on preliminary data obtained from this screening effort with three specific aims. In the first, experiments are proposed to characterize previously identified, strong screening hits in order to confirm specificity, define potency, and characterize activity spectrum in L. pneumophila, Coxiella burnetii and a series of more distantly related T4SS-dependent pathogens. In the second, iterative structure-activity relationship studies will be used to identify analogues with the enhanced pharmacological potential. In the third, the activity of select small molecule inhibitors will be characterized in ivo in murine models of infection with L. pneumophila, C. burnetii, and Bartonella. Taken together these experiments should establish the theoretical basis for T4SS therapy and its potential use as a new human therapeutic.
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会议论文
De Novo Synthesis, and Functional and Structural Characterization of Novel Aminoglycoside Analogues to Bypass Resistance Mechanisms and Optimize Selectivity
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批准号:10676201
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项目类别:
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资助金额:$75.72万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
Use of De Novo Synthesis Approaches and Structure-guided Design to Optimize Therapeutic Properties of Streptothricin Class Antimicrobials
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批准号:10469007
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项目类别:
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资助金额:$77.22万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
De Novo Synthesis, and Functional and Structural Characterization of Novel Aminoglycoside Analogues to Bypass Resistance Mechanisms and Optimize Selectivity
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批准号:10447128
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项目类别:
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资助金额:$76.53万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
Use of De Novo Synthesis Approaches and Structure-guided Design to Optimize Therapeutic Properties of Streptothricin Class Antimicrobials
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批准号:10269053
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项目类别:
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资助金额:$77.75万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
Use of De Novo Synthesis Approaches and Structure-guided Design to Optimize Therapeutic Properties of Streptothricin Class Antimicrobials
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批准号:10686110
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项目类别:
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资助金额:$76.68万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
De Novo Synthesis, and Functional and Structural Characterization of Novel Aminoglycoside Analogues to Bypass Resistance Mechanisms and Optimize Selectivity
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批准号:10242923
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资助金额:$77.26万
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财政年份:2020
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负责人:JAMES E KIRBY
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依托单位:
Fusidic acid derivatization to enhance entry into Gram-negative pathogens
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批准号:9807473
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项目类别:
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资助金额:$26.61万
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财政年份:2019
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负责人:JAMES E KIRBY
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依托单位:
VALIDATION OF A HIGH THROUGHPUT SCREEN FOR KPC PLASMID EVICTION
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批准号:8891557
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资助金额:$21.75万
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财政年份:2015
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负责人:JAMES E KIRBY
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依托单位:
Plasmid Eviction to Restore Susceptibility in Carbapenem-Resistant Enterobacteriaceae
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批准号:8954519
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项目类别:
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资助金额:$13.05万
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财政年份:2015
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负责人:JAMES E KIRBY
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依托单位:
VALIDATION OF A HIGH THROUGHPUT SCREEN FOR KPC PLASMID EVICTION
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批准号:8990439
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项目类别:
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资助金额:$26.1万
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财政年份:2015
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负责人:JAMES E KIRBY
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依托单位:
Novel Antimicrobials Targeting Bacterial Type IV Secretion Systems
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批准号:8439168
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项目类别:
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资助金额:$39.0万
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财政年份:2012
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负责人:JAMES E KIRBY
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依托单位:
Novel Antimicrobials Targeting Bacterial Type IV Secretion Systems
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批准号:9123514
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项目类别:
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资助金额:$39.15万
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财政年份:2012
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负责人:JAMES E KIRBY
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依托单位:
Type IV Secretion System Therapeutics
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批准号:7896197
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项目类别:
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资助金额:$21.71万
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财政年份:2010
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负责人:JAMES E KIRBY
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依托单位:
Type IV Secretion System Therapeutics
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批准号:8041056
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项目类别:
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资助金额:$25.84万
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财政年份:2010
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负责人:JAMES E KIRBY
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依托单位:
Non-Antibiotic Selectable Markers for Bacillus Anthracis
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批准号:7565913
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项目类别:
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资助金额:$34.83万
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财政年份:2008
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负责人:JAMES E KIRBY
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依托单位:
Non-Antibiotic Selectable Markers for Bacillus Anthracis
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批准号:7472107
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项目类别:
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资助金额:$21.25万
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财政年份:2008
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负责人:JAMES E KIRBY
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依托单位:
The Basis of Anthrax-Induced Vascular Damage
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批准号:6985044
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项目类别:
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资助金额:$21.25万
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财政年份:2005
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负责人:JAMES E KIRBY
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依托单位:
The Basis of Anthrax-Induced Vascular Damage
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批准号:7140530
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项目类别:
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资助金额:$20.75万
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财政年份:2005
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负责人:JAMES E KIRBY
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依托单位:
LEGIONELLA PNEUMOPHILA VIRULENCE FACTORS DEFINED IN VIVO
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批准号:2442371
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项目类别:
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资助金额:$8.26万
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财政年份:1996
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负责人:JAMES E KIRBY
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依托单位:
LEGIONELLA PNEUMOPHILA VIRULENCE FACTORS DEFINED IN VIVO
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批准号:2886030
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项目类别:
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资助金额:$0.55万
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财政年份:1996
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负责人:JAMES E KIRBY
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依托单位:
海外基金