Genetic Analysis of Interactions Between Oral Innate Immunity and a Herpesvirus

口腔先天免疫与疱疹病毒之间相互作用的遗传分析

• 批准号: 7487775
• 负责人: TING-TING WU
• 金额: $ 19.04万
• 依托单位: UNIVERSITY OF CALIFORNIA LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-22 至 2010-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7487775
• 关键词: A Mouse; Antiviral Response; Body part; Cells; Collection; Equilibrium; Fibroblasts; Genes; Genetic; Genome; Goals; Herpesviridae; Human; Immune system; Immunocompetent; Infection; Knockout Mice; Laboratories; Microbe; Mouse Strains; Mus; Open Reading Frames; Oral; Oral Administration; Oral cavity; Pathogenesis; Proteins; Role; Salivary Glands; Satellite Viruses; Signal Pathway; Simplexvirus; System; Viral; Viral Genes; Viral Genome; Virus; Virus Diseases; genetic analysis; in vivo; insight; mouse model; mutant; oral innate immunity; oral pathogen; reactivation from latency; virus host interaction

DESCRIPTION (provided by applicant): The oral cavity represents a unique body part that is in contact with the external world and therefore constantly encounters a vast diverse of microbes. Herpesviruses are significant resident oral pathogens in humans. However, little is known about how the host senses and responds to herpesviruses during primary infection, latency and reactivation in the oral cavity, especially in regards to the innate immune system. Coexistence of a virus and its immunocompetent host entails a delicate balance between viral replication and host clearance. Elucidating the interactions between the innate immune system and herpesviruses will provide insights to how the balance is accomplished and regulated. A mouse model of murine gammaherpesvirus-68 (MHV-68) infection provides an excellent system to explore virus-host interactions in the oral cavity for several reasons. First, following oral administration, MHV-68 replicates in the oronasal cavity and the salivary gland. Second, an amenable genetic system is available to mutagenize the MHV-68 viral genome. Third, MHV-68 infects a variety of laboratory strains of mice, which allows the role of cellular genes during viral infection to be studied in vivo. The long-term goal of our discovery driven approach is to determine the role of viral and cellular proteins in virus-associated pathogenesis by employing knock-out mice and a collection of MHV-68 mutant viruses. The MHV-68 genome is randomly disrupted by an insertion of a transponson. There are 32 viral ORFs that are not required for replication in fibroblast cells and potentially involved in modulating virus-host interactions. The object of this exploratory R21 application is to define the in vivo sensing and defending role of TLR and its signaling pathway using a mouse model of oral MHV-68 infection. Furthermore, we will systematically screen viral genes that are capable of inhibiting the activation of anti-viral responses in cells, an essential step for understanding virus-host interactions.

描述（由申请人提供）：口腔代表与外部世界接触的独特身体部位，因此不断遇到大量的微生物。疱疹病毒是人类中重要的居民口腔病原体。然而，关于宿主在原发性感染，口腔中的潜伏期和重新激活期间的感觉和响应鲜明，尤其是在先天免疫系统方面，知之甚少。病毒及其免疫能力宿主的共存需要在病毒复制和宿主间隙之间取得微妙的平衡。阐明先天免疫系统与疱疹病毒之间的相互作用将为平衡的实现和调节提供见解。小鼠γγ型病毒68（MHV-68）感染的小鼠模型为探索口腔中病毒宿主相互作用的出色系统提供了多种原因。首先，在口服后，MHV-68在Oronasal腔和唾液腺中复制。其次，可以使用正式的遗传系统来诱变MHV-68病毒基因组。第三，MHV-68感染各种实验室菌株的小鼠，这使得在体内研究病毒感染中细胞基因的作用。 我们发现驱动方法的长期目标是确定病毒和细胞蛋白在病毒相关的发病机理中的作用，并采用敲除小鼠和收集的MHV-68突变病毒。 MHV-68基因组被转录的插入随机破坏。在成纤维细胞中复制不需要32个病毒ORF，并可能参与调节病毒宿主相互作用。该探索性R21应用的对象是使用口服MHV-68感染的小鼠模型来定义TLR及其信号通路的体内感应和防御作用。此外，我们将系统地筛选能够抑制细胞中抗病毒反应激活的病毒基因，这是理解病毒宿主相互作用的重要步骤。