Defining the role of Serratia marcescens nuclease in infection process
定义粘质沙雷氏菌核酸酶在感染过程中的作用
基本信息
- 批准号:10646829
- 负责人:
- 金额:$ 7.4万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-02-06 至 2025-01-31
- 项目状态:未结题
- 来源:
- 关键词:AddressAffectAnatomyAnimal ModelAntibioticsBacteriaBacterial Drug ResistanceBiologicalBiologyBlood CirculationCathetersCell Culture TechniquesCellsCessation of lifeClinicalDataDevelopmentDialysis patientsDoseEnzymesEvaluationExcisionEyeFrequenciesFutureGoalsGram-Negative BacteriaGrowthHL-60 CellsHealthcareHemodialysisHigh PrevalenceHospitalsImmune EvasionImmune responseInfectionKidney FailureKnowledgeMediatingModelingMorbidity - disease rateMulti-Drug ResistanceMusNeutrophil InfiltrationOrganismOutcomePathogenesisPatientsPeritoneal DialysisPeritonitisPlayPositioning AttributePre-Clinical ModelPredispositionProcessResearchResistanceResolutionRoleSWR/J MouseSerratiaSerratia InfectionsSerratia marcescensSignal TransductionSiteSurgical woundSystemSystemic infectionTestingTimeTissuesUrinary tractVirulence FactorsWorld Health Organizationantimicrobialendonucleaseexperimental studyextracellularin vivoin vivo imaginginsightintraperitonealmouse modelmutantneutrophilnovelnucleaseopportunistic pathogenpathogenpathogenic bacteriapriority pathogenrational designrespiratoryspatiotemporalsugar
项目摘要
Project Summary
The emergence of bacterial drug resistance, especially in hospital settings, represents the next
great challenge in healthcare. Serratia marcescens, the Gram-negative bacterial pathogen with
intrinsic resistance to several classes of antibiotics, can cause infections with severe outcomes
affecting multiple body sites. This bacterium is also associated with complications of peritoneal
dialysis (PD) in patients with kidney failure. Importantly, Serratia-associated peritonitis
accompanied by massive neutrophil infiltration was shown to have the highest nonresolution rate
among episodes caused by Gram-negative bacteria, leading either to the death of the PD patient,
or catheter removal and transfer to hemodialysis. The progress in our understanding of S.
marcescens infections is hampered by the lack of reliable preclinical model, which represents a
critical barrier to progress in the field. The current knowledge of strategies used by this
opportunistic pathogen to colonize the mammalian host and to evade the immune response is not
complete, and only a handful of virulence factors were identified to date. S. marcescens is known
to secrete an array of hydrolytic enzymes, including sugar non-specific endonuclease; however,
the biological role of this enzyme during infection has not been evaluated. In this proposal, we
seek to establish a murine model to study the S. marcescens dynamic spread during
intraperitoneal infection and to test a hypothesis that an extracellular S. marcescens enzyme
nuclease plays a key role in bacterial escape from neutrophil extracellular traps (NETs) in this
niche. In Aim 1 we will characterize the bioluminescent S. marcescens spread following
intraperitoneal infection using in vivo imaging. In Aim 2 we will first evaluate the S. marcescens
extracellular nuclease potential to degrade NETs in cultures of neutrophil-like cells, followed by
infection study to determine the biological role of this enzyme in vivo. This proposal will advance
current understanding of Serratia pathogenesis and provide insight into the bacterium’s strategy
to avoid neutrophil-mediated clearance. Altogether, our experiments will establish a blueprint for
future studies of other nuclease-producing pathogenic bacteria.
项目概要
细菌耐药性的出现,尤其是在医院环境中,代表着下一个
粘质沙雷氏菌(Serratia marcescens)是一种革兰氏阴性细菌病原体,在医疗保健方面面临着巨大的挑战。
对几类抗生素的内在耐药性,可能导致严重后果的感染
这种细菌还与腹膜并发症有关。
重要的是,沙雷氏菌相关性腹膜炎患者进行透析(PD)。
伴有大量中性粒细胞浸润的不解决率最高
由革兰氏阴性菌引起的事件,导致帕金森病患者死亡,
或导管移除并转移至血液透析 我们对 S. 的了解进展。
粘质杆菌感染因缺乏可靠的临床前模型而受到阻碍,这代表了
目前对该领域所使用的策略的了解是阻碍该领域取得进展的关键障碍。
机会性病原体定植于哺乳动物宿主并逃避免疫反应,这并不是
完整的,并且迄今为止仅确定了少量粘质沙门氏菌的毒力因子。
然而,分泌一系列水解酶,包括糖非特异性核酸内切酶;
在本提案中,我们尚未评估这种酶在感染过程中的生物学作用。
寻求建立小鼠模型来研究 S. marcescens 的动态传播
腹膜内感染并检验细胞外粘质沙门氏菌酶的假设
核酸酶在细菌逃离中性粒细胞胞外陷阱(NET)的过程中发挥着关键作用
在目标 1 中,我们将描述生物发光粘质沙门氏菌传播的特征。
在目标 2 中,我们将首先评估粘质沙门氏菌。
细胞外核酸酶有可能降解中性粒细胞样细胞培养物中的 NET,然后
这一提议将推进确定这种酶在体内的生物学作用的感染研究。
目前对沙雷氏菌发病机制的了解并提供对该细菌策略的深入了解
为了避免中性粒细胞介导的清除,我们的实验将建立一个蓝图。
其他产生核酸酶的致病细菌的未来研究。
项目成果
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