Structure-function analysis of type IVB secretion systems
Structure-function analysis of type IVB secretion systems
批准号:
10624264
负责人:
Michael G. Caparon
金额:
$51.18万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-06-10 至 2024-05-31
关键词:
AddressAlveolar MacrophagesBacteriaBacterial InfectionsBindingCell NucleusCell physiologyCellsComplexCouplingCoxiellaCryoelectron MicroscopyCytoplasmDNADedicationsDevelopmentDiseaseDrug TargetingDrug usageEnvironmentEukaryotaFamilyFutureGenesGoalsGram-Negative BacteriaGrowthHealthHumanImageIndividualKnowledgeLegionellaLegionella pneumophilaLegionnaires&apos DiseaseLightLungLysosomesMacromolecular ComplexesMacrophageMediatingMembraneMolecularMolecular ChaperonesOrganismPathway interactionsPhagocytesPhagosomesPharmacotherapyPhasePlasmidsPneumoniaProteinsProtozoaResearchRhizobium radiobacterRoleStructureSystemTherapeuticTherapeutic InterventionType IV Secretion System PathwayVacuoleVirulenceVirulence FactorsVisualizationbactericidecell envelopedrug developmentfollow-upinsightmolecular targeted therapiesmultidisciplinarymutantnovelpathogenpathogenic bacteriapreventreceptorsecretion processtargeted treatmenttrait
中文摘要
摘要
英文摘要
Abstract
Legionella pneumophila is a Gram-negative bacteria that replicates inside protozoa in the environment but
can also replicate within alveoloar macrophages, thereby causing a pneumonia-like disease called
Legionnaires’ disease. L. pneumophila is able to survive and replicate within normally bactericidal
phagocytic cells by altering their endocytic pathway and preventing rapid phagosome-lysosome fusion. L.
pneumophila perturbs normal host cell function by injecting a large number of virulence factors into the host
cell cytoplasm via a type IVB secretion system (T4BSS). The L. pneumophila T4BSS is encoded by twenty-
seven dot/icm genes, which encode a large macromolecular complex in the bacterial cell envelope. The
Dot/Icm system is absolutely required for intracellular growth and virulence. In contrast, the majority of the
~300 Dot/Icm substrates appear to be dispensable for both traits due to multiple levels of redundancy.
Therefore, the L. pneumophila Dot/Icm represents the most viable target for therapeutic intervention.
Although a significant amount of information has been acquired about the assembly and function of the
Dot/Icm system, many questions remain. This proposal will follow-up on a number of recent advances on
the Dot/Icm T4BSS. These include the discovery that the Dot/Icm system is located at the poles of the
bacterium and polar export of substrates by this specialized secretion system is required for proper
intracellular targeting of the LCV (Legionella containing vacuole). The second major advance was the
determination of the structure of the c-terminus of DotL bound to the secretion chaperones. The final
advance was the acquisition of the first image of this secretion apparatus by cryoEM. Overall this research
relates to human health in several ways. First, establishing the mechanism used by L. pneumophila to
survive and replicate inside macrophages will provide additional insight into how it causes disease and may
reveal novel targets to be used for drug therapy. Second, since specialized secretion systems are
commonly used by a variety of bacterial pathogens, knowledge gained about the L. pneumophila secretion
apparatus is likely to be applicable to understanding the molecular mechanisms of virulence used by other
pathogens, and could serve as the basis to prevent or treat a number of different diseases.
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资助金额:$38.13万
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财政年份:2007
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资助金额:$34.2万
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海外基金