Inhibitors of Type VI Sectretion in NIAID Priority Pathogens
Inhibitors of Type VI Sectretion in NIAID Priority Pathogens
批准号:
7669813
负责人:
STEPHEN LORY
金额:
$31.75万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-03-25 至 2014-02-28
关键词:
Animal ModelAnimalsAntibiotic TherapyBiologicalBiological AssayBiological WarfareBiologyBioterrorismBurkholderiaBurkholderia malleiBurkholderia pseudomalleiCategoriesCellsChemicalsChromosomesContainmentCytoplasmDevelopmentDrug KineticsEmerging Communicable DiseasesEnvironmentEukaryotic CellGene ClusterGeneticGlandersHousingInfectionLaboratoriesLeadLibrariesLocationMalleusMelioidosisModificationNational Institute of Allergy and Infectious DiseaseNew EnglandOrganismPathway interactionsPlayProtein translocationProteinsRoleScreening procedureSiteStructure-Activity RelationshipSystemTestingTherapeuticTherapeutic AgentsToxic effectVaccinesVirulenceVirulence FactorsWorkantimicrobialantimicrobial drugbasebiodefenseefficacy testingextracellularhigh throughput screeninginhibitor/antagonistmedical schoolsmicroorganismmortalitynovelpathogenpre-clinicalprogramsprotein complextherapeutic vaccinevaccine development
中文摘要
点击翻译按钮获取中文摘要
英文摘要
A number of pathogenic microorganisms, including, several NIAID Priority Pathogens, secrete virulence
factors utilizing a novel pathway referred to as the type VI secretion system (T6SS). The main objective of
this project is to develop inhibitors of T6SS that could lead to a new class of antimicrobial agents.
Burkholderia thailandensis will be used to identify T6SS inhibitors compounds in a high throughput screen
and these will be tested for interference with secretion in several category A-C select agents, including
Burkholderia pseudomallei and Burkholderia mallei, causative agents of melioidosis and glanders,
respectively. The candidate inhibitors of T6SS and their structural derivatives will be used in subsequent
studies, which include demonstration of their efficacy in an animal model of melioidosis. The T6SS
components, targeted by the active compounds will be identified. The work proposed in this project
represents a logical pre-clinical development strategy for therapeutic agents targeting several agents of
biological warfare and bioterrorism.
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海外基金