Virulence Factors of Stenotrophomonas maltophilia
Virulence Factors of Stenotrophomonas maltophilia
批准号:
7739151
负责人:
NICHOLAS P CIANCIOTTO
金额:
$7.63万
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:
2009-07-22 至 2011-06-30
关键词:
AddressBacteriaBehaviorBeliefBloodComplementDataDiseaseEnzymesEyeFimbriae ProteinsFutureGenesGenomeGrantHeartHumanInfectionInvestigationLeadLegionella pneumophilaLocalesLungModelingMusMutateNosocomial pneumoniaOrganismPathogenesisPathologyPilot ProjectsPilumPneumoniaPreventionProtein SecretionProteinsPseudomonas aeruginosaPublishingResearchRespiratory SystemRespiratory Tract InfectionsRespiratory tract structureRoleSkinStenotrophomonas maltophiliaSurfaceSystemTestingTissuesToxinType II Secretion System PathwayUnited States National Institutes of HealthUrinary tractVirulenceVirulence FactorsVirulentWorkappendagecommunicable disease diagnosisdisease diagnosisgenome sequencinghuman diseasemutantpathogenprogramspublic health relevancesoft tissue
中文摘要
描述(由申请人提供):嗜麦芽窄养单胞菌是一种环境细菌,与越来越多的人类疾病有关,包括肺、血液、心脏、泌尿道、中枢神经系统、眼睛、皮肤和软组织的感染。呼吸道是嗜麦芽葡萄球菌最常见的地方,约5%的院内肺炎与该菌有关。然而,对嗜麦芽葡萄球菌感染肺部的方式知之甚少。因此,本研究旨在确定嗜麦芽葡萄球菌促进肺部感染及其发病机制的因子。我们的实验室和其他人的工作已经确定,II型蛋白分泌(T2S)是肺病原体(包括铜绿假单胞菌和嗜肺军团菌)毒力的主要促进因素。T2S分泌的蛋白质通常包括毒素和组织降解酶。因此,我们假设T2S在嗜麦芽链球菌的发病机制中起关键作用。为了验证这一点,我们将对嗜麦芽葡萄球菌基因组测序所揭示的编码T2S装置的基因进行突变,然后在嗜麦芽葡萄球菌肺部感染小鼠模型中检测突变体。降低突变体感染和/或损害肺部的能力将引发未来对效应物的追求。其他过去的研究表明IV型菌毛(T4P)促进肺部感染,最近的测序也表明嗜麦芽葡萄球菌编码这种类型的表面附属物。因此,我们假设嗜麦芽链球菌的T4P是疾病的另一个促进者。为了解决这个问题,我们将测试嗜麦芽链球菌T4P突变体在小鼠肺中的行为。获得的数据有可能导致新形式的传染病诊断、治疗或预防。公共卫生相关性:嗜麦芽窄养单胞菌是一种环境细菌,与越来越多的人类感染有关,包括肺、血液、心脏、尿路、中枢神经系统、眼睛、皮肤和软组织的感染。呼吸道是嗜麦芽葡萄球菌最常见的地方,约5%的院内肺炎与该菌有关。然而,对嗜麦芽葡萄球菌感染肺部的方式知之甚少。因此,本研究的目的是确定嗜麦芽葡萄球菌促进肺部感染的因子,重点关注生物体的IV型菌毛和II型分泌系统分泌的蛋白质。
英文摘要
DESCRIPTION (provided by applicant): Stenotrophomonas maltophilia is an environmental bacterium that is implicated in an increasing spectrum of human disease, including infections of the lung, blood, heart, urinary tract, CNS, eyes, skin, and soft tissue. The respiratory tract is the most common locale for S. maltophilia, with ca. 5% of nosocomial pneumonias being associated with the organism. However, very little is known about the way in which S. maltophilia infects the lung. Thus, this proposal aims to identify S. maltophilia factors that promote lung infection and pathogenesis. Work from our lab and others have determined that type II protein secretion (T2S) is a major facilitator of virulence in lung pathogens, including Pseudomonas aeruginosa and Legionella pneumophila. Proteins secreted by T2S usually include toxins and tissue-degrading enzymes. Thus, we hypothesize that T2S is critical in S. maltophilia pathogenesis. To test this, we will mutagenize genes encoding the T2S apparatus that have been revealed by the sequencing of the S. maltophilia genome and then examine the mutants in the murine model of S. maltophilia lung infection. A reduction in the capacity of the mutants to infect and/or damage the lung would trigger the future pursuit of effectors. Other past work has shown that type IV pili (T4P) promote lung infection, and recent sequencing has also shown that S. maltophilia encodes this type of surface appendage. Thus, we posit that the T4P of S. maltophilia is another facilitator of disease. To address this, we will test T4P mutants of S. maltophilia for their behavior in the murine lung. The data obtained have the potential to lead to new forms of infectious disease diagnosis, treatment, or prevention. PUBLIC HEALTH RELEVANCE: Stenotrophomonas maltophilia is an environmental bacterium that has been implicated in an increasing spectrum of human infections, including infections of the lung, blood, heart, urinary tract, CNS, eyes, skin, and soft tissue. The respiratory tract is the most common locale for S. maltophilia, with approximately 5% of nosocomial pneumonias being associated with the organism. However, very little is known about the way in which S. maltophilia infects the lung. Thus, it is the intent of this proposed research to identify S. maltophilia factors that promote lung infection with a focus on the organism's type IV pili and the proteins secreted via the type II secretion system.
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会议论文
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