New approaches to study Pseudomonas-host interactions
New approaches to study Pseudomonas-host interactions
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
中文摘要
描述(由申请人提供):病原体突破高度极化的宿主粘膜上皮屏障的能力是微生物感染发病机制中早期和关键的一步。这一事件对铜绿假单胞菌(PA)等机会性病原体尤其关键,PA是人类最致命的机会性病原体之一。我们的长期目标是了解病原体,特别是PA是如何克服宿主上皮屏障而导致人类疾病的。PA与极化上皮细胞的顶端(AP)表面结合,并触发宿主细胞的根本性变化,从而允许细菌内化。在此期间,我们发现PA诱导AP表面的形态发生显著的局部变化,形成由基底外侧(BL)成分组成的膜性突起。这个突起可能是细菌进入的管道。AP膜局部特性的这种深刻变化是PA对上皮细胞单层影响的第一个已知的形态标志。根据我们的数据,我们假设PA可以利用粘膜屏障上皮极性的小缺陷来启动一系列事件,导致正反馈循环,导致AP膜向BL膜转变的显著形态变化。形成具有新生AJ特征的突起,其功能是作为细菌进入的管道。通过操纵上皮细胞的极性,PA能够增强其细菌的结合和进入,可能是通过增加宿主细胞受体的呈递或其他促进内化的因素。我们的目标是(1)确定TJ和AJ的哪些关键调节和结构成分被招募到突起中。(2)确定突起形成和细菌侵入之间的时间和功能关系。(3)进行机制研究,以揭示PA如何劫持宿主细胞的囊泡运输,从而将这些连接成分和BL成分重新定向到AP表面。(4)确定形成突起的细菌决定因素。总之,这些研究将全面剖析PA和宿主细胞上皮之间的相互作用。他们将确定细菌利用来致病的宿主因素。利用病原体研究哺乳动物生物学中的基本过程,如上皮极性的建立和维持,除了在发病机制之外,还在许多领域有广泛的分支,包括癌症和发育生物学。此外,这些宿主细胞因子可能成为抗菌疗法发展的新靶点;因为药物针对宿主而不是细菌分子,与传统的抗微生物疗法相比,它们产生耐药性的可能性要小得多。
公共卫生相关性:铜绿假单胞菌是一种细菌,是住院或免疫功能低下患者感染的最常见原因之一。假单胞菌能够直接进入细胞,这在其致病能力方面很重要。我们正在研究它进入细胞的机制。这可能会导致新的治疗方法。
英文摘要
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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海外基金