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Identification and Analysis of Host Factors that Support Brucella Infection

Identification and Analysis of Host Factors that Support Brucella Infection
支持布鲁氏菌感染的宿主因素的鉴定和分析
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

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中文摘要
翻译
描述(申请人提供):羊布鲁氏菌是一种具有全球意义的人和动物细菌性病原体。尽管细菌因素介导宿主-病原体的相互作用已被揭示,但对白念珠菌进入哺乳动物细胞并在哺乳动物细胞中复制具有重要作用的宿主因素仍不清楚。我们最近利用了一种新的布鲁氏菌感染的果蝇黑腹果蝇S2细胞模型来进行支持这种细胞内病原体复制的宿主因素的初步筛选。我们的筛查发现了已经被证实对羊白念珠菌16M株(Bm16M)进入哺乳动物细胞和在细胞内运输具有重要作用的基因。此外,我们的屏幕发现了几个在哺乳动物细胞模型中得到验证的新命中。在这里,我们建议利用这些发现来进行大规模的RNAi筛查,以寻找额外的宿主因素。具体地说,我们的目标是:(1)对干扰或增强蜜蜂对果蝇S2细胞感染的RNA进行大规模筛选;(2)将HIT分为表型和功能类别,并将所获得的结果与最近完成的偶发分枝杆菌和单核细胞增多性李斯特菌筛查的结果进行比较。最后,我们将利用siRNA技术来检查在我们的果蝇S2细胞筛选中获得的HITS的哺乳动物同源基因是否介导了哺乳动物细胞的Bm16M感染。综上所述,这些实验将定义更多的宿主因素,支持白念珠菌在动物细胞中的吸收和复制,从而为调节这一重要的宿主-病原体相互作用的分子机制提供新的见解。 这项建议将确定和表征介导羊种布鲁氏菌感染动物细胞的新宿主因素。因此,我们预计这一努力将有助于我们对这种具有全球意义的病原体的了解,并通过发现可能的治疗干预的潜在蛋白质靶标,从而使公众健康受益。与公共卫生的相关性。 本提案将确定和表征介导布鲁氏菌的新宿主因素 羊毛虫对动物细胞的感染。我们期望这一努力将因此受益。 公共卫生通过显著促进我们对这一全球疾病病原体的理解 意义,并通过发现潜在的蛋白质靶点可能的治疗 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