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New approaches to study Pseudomonas-host interactions

New approaches to study Pseudomonas-host interactions
研究假单胞菌与宿主相互作用的新方法
批准号:
8278542
负责人:
Joanne N. Engel
金额:
$34.41万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-05-01 至 2014-05-31
关键词:
ADP Ribose TransferasesAbbreviationsAdherens JunctionAdhesionsAnti-Bacterial AgentsApicalBacteriaBindingBiologyCancer BiologyCanis familiarisCell PolarityCellsCellular StructuresCharacteristicsChemicalsChinese HamsterCollaborationsCollectionComplexConfocal MicroscopyCystic FibrosisCytochalasin DCytoplasmDataDefectDevelopmentDevelopmental BiologyDiseaseDominant-Negative MutationDouble-Stranded RNADrug Delivery SystemsE-CadherinEGF geneEpidermal Growth FactorEpidermal Growth Factor ReceptorEpithelialEpithelial CellsEpitheliumEventFeedbackFlagellaGTPase-Activating ProteinsGoalsGrantGrowth FactorGrowth Factor ReceptorsHelicobacter pyloriHeparan Sulfate ProteoglycanHumanImageImmune systemImmunocompromised HostImmunofluorescence ImmunologicInfectionInjuryIntegration Host FactorsKidneyKineticsLeadLipidsMaintenanceMediator of activation proteinMembraneMicroscopyMorbidity - disease rateMorphologyNeisseria meningitidisOvaryPH DomainPathogenesisPhosphatidylinositolsPhosphotransferasesPilumPlatelet-Derived Growth FactorProcessProductionProtein KinaseProteinsProto-Oncogene Proteins c-aktPseudomonasPseudomonas aeruginosaRNA InterferenceRNA-Induced Silencing ComplexReceptor CellRecruitment ActivityRegulationResistanceSeriesSignal TransductionSmall Interfering RNASurfaceSystemTestingTherapeuticTight JunctionsTimeTransferaseTransgenesType III Secretion System PathwayVirulentWound Healingantimicrobialapical membranebasebasolateral membranecell typeenteropathogenic Escherichia colihuman diseaseinhibitor/antagonistinorganic phosphatelatrunculin Amanmicrobialmicroorganismmonolayermortalitymutantnectinnovelnovel strategiesnovel therapeutic interventionpathogenphosphoinositide-3,4,5-triphosphatephosphoinositide-3,4-bisphosphatepreventprotein Epublic health relevancered fluorescent proteintime usetraffickingtrans-Golgi Network

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DESCRIPTION (provided by applicant): The ability of a pathogen to breach the highly polarized host mucosal epithelial barrier is an early and critical step in the pathogenesis of microbial infections. This event is particularly crucial for opportunistic pathogens such as Pseudomonas aeruginosa (PA), one of the most virulent opportunistic pathogens of man. Our long-term goals are to understand how pathogens in general, and PA in particular, overcome the host epithelial barrier to cause human disease. PA binds to the apical (AP) surface of polarized epithelial cells and triggers fundamental changes in the host cell that allow bacterial internalization. During this granting period, we have discovered that PA induces a remarkable local change in the morphology of the AP surface to form a membranous protrusion composed of basolateral (BL) constituents. This protrusion is the likely conduit for bacterial entry. This profound shift in the local identity of the AP membrane is the first known morphologic landmark of the effect of PA on epithelial cell monolayers. Based on our data, we hypothesize that PA can exploit small defects in epithelial polarity at the mucosal barrier to initiative a series of events that result in a positive feedback loop induces a remarkable morphologic change in which AP membrane is transformed into BL membrane. A protrusion, with characteristics of a nascent AJ, is formed that functions as a conduit for bacterial entry. By manipulating epithelial cell polarity, PA is able to enhance its bacterial binding and entry, possibly by increasing the presentation of host cell receptors or other factors that promote internalization. Our aims are to (1) Determine which key regulatory and structural components of TJ and AJ are recruited to the protrusion. (2) Determine the temporal and functional relationship between protrusion formation and bacterial entry. (3) Perform mechanistic studies to uncover how PA hijacks host cell vesicular trafficking to redirect these junctional and BL components to the AP surface. (4) Identify the bacterial determinants of protrusion formation. Together, these studies will comprehensively dissect the interactions between PA and host cell epithelium. They will identify host factors that the bacteria exploit to cause disease. The use of pathogens to study fundamental processes in mammalian biology, such as the establishment and the maintenance of epithelial polarity, has broad ramifications for many fields in addition to pathogenesis, including cancer and developmental biology. Furthermore, these host cell factors may serve as novel targets for the development of anti-bacterial therapeutics; because the drug targets host but not bacterial molecules, they are much less likely to engender resistance compared to conventional anti- microbial therapies. PUBLIC HEALTH RELEVANCE: Pseudomonas aeruginosa is a bacterium that is one of the most frequent causes of infections in hospitalized or immunocompromised patients. Pseudomonas is able to directly enter into cells and this is important in its ability to cause disease. We are investigating the mechanisms by which it enters into cells. This may lead to novel therapeutic approaches.
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