Identification and Analysis of Host Factors that Support Brucella Infection
Identification and Analysis of Host Factors that Support Brucella Infection
批准号:
7903743
负责人:
PAUL DE FIGUEIREDO
金额:
$9.97万
依托单位:
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:
2009-09-12 至 2010-08-31
关键词:
AnimalsBiological ModelsBrucellaBrucella melitensisCategoriesCell modelCellsDataDrosophila genusDrosophila melanogasterEmbryoEndoplasmic ReticulumFibroblastsGenesHumanInfectionInositolInsectaIntegration Host FactorsListeria monocytogenesMammalian CellMediatingMolecularMusMycobacterium fortuitumOrthologous GenePhosphotransferasesProteinsPublic HealthRNA InterferenceSmall Interfering RNASystemTechnologyTherapeutic Interventioninsightknock-downnovelpathogenpublic health relevanceresearch studytraffickinguptake
中文摘要
性状(由申请方提供):羊种布鲁氏菌是一种具有全球意义的人类和动物细菌病原体。虽然介导宿主-病原体相互作用的细菌因子已经被揭示,但是对于B.在哺乳动物细胞中的羊种进入和复制仍然不清楚。我们最近开发了一种新的果蝇S2细胞模型布鲁氏菌感染进行试点筛选宿主因子,支持这种细胞内病原体的复制。我们的筛选发现了已经被确定为对B重要的基因。羊种布氏菌菌株16 M(Bm 16 M)进入和哺乳动物细胞中的细胞内运输。此外,我们的筛选发现了几个在哺乳动物细胞模型中验证的新命中。在这里,我们建议利用这些发现来进行大规模的RNAi筛选,以寻找其他宿主因子。具体而言,我们的目标是:(1)进行大规模筛选破坏或增强B的RNAi。Melitensis感染的果蝇S2细胞;(2)将命中分类为表型和功能类别,并将获得的结果与最近完成的偶发分枝杆菌和单核细胞增生李斯特菌筛选的结果进行比较。最后,我们将采用siRNA技术来检查在我们的果蝇S2细胞筛选中获得的命中的哺乳动物直系同源物是否介导Bm 16 M感染哺乳动物细胞。总之,这些实验将确定支持B摄取和复制的其他宿主因子。melitensis进入动物细胞,从而提供新的见解介导这一重要的宿主-病原体相互作用的分子机制。
本提案将鉴定和表征介导羊种布氏杆菌感染动物细胞的新型宿主因子。我们希望这项工作将因此有益于公共卫生,有助于我们了解这种具有全球意义的病原体,并发现潜在的蛋白质靶点进行可能的治疗干预。公共卫生相关性。
该提案将鉴定和表征介导布鲁氏菌的新宿主因子
Melitensis感染动物细胞。我们希望,这一努力将因此受益。
通过对我们对这种全球性病原体的了解做出重大贡献,
重要性,并通过发现潜在的蛋白质靶点,
干预
英文摘要
DESCRIPTION (provided by applicant): Brucella melitensis is a human and animal bacterial pathogen of global significance. Although bacterial factors mediating the host-pathogen interaction have been revealed, host factors that are important for B. melitensis entry and replication in mammalian cells remain obscure. We have recently exploited a novel Drosophila melanogaster S2 cell model of Brucella infection to perform a pilot screen for host factors that support the replication of this intracellular pathogen. Our screen uncovered genes that have already been established as being important for B. melitensis strain 16M (Bm16M) entry and intracellular trafficking in mammalian cells. In addition, our screen uncovered several novel hits that were validated in mammalian cell models. Here, we propose to exploit these findings to perform a large-scale RNAi screen for additional host factors. Specifically, we aim: (1) To perform a large-scale screen for RNAis that disrupt or enhance B. melitensis infection of Drosophila S2 cells; (2) To classify hits into phenotypic and functional categories, and to compare the results obtained to those from the recently completed Mycobacterium fortuitum and Listeria monocytogenes screens. Finally, we shall employ siRNA technology to examine whether the mammalian orthologs of the hits obtained in our Drosophila S2 cell screen mediate Bm16M infection of mammalian cells. Taken together, these experiments will define additional host factors that support the uptake and replication of B. melitensis into animal cells, and thereby provide new insights into the molecular mechanisms mediating this important host-pathogen interaction.
This proposal shall identify and characterize novel host factors mediating Brucella melitensis infection of animal cells. We expect that this effort shall therefore benefit public health by contributing significantly to our understanding of this pathogen of global significance, and by discovering potential protein targets for possible therapeutic intervention. Public Health Relevance.
This proposal shall identify and characterize novel host factors mediating Brucella
melitensis infection of animal cells. We expect that this effort shall therefore benefit
public health by contributing significantly to our understanding of this pathogen of global
significance, and by discovering potential protein targets for possible therapeutic
intervention.
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海外基金