MOLECULAR BASIS OF PERSISTENT VIRUS INFECTION

持续病毒感染的分子基础

• 批准号: 3138622
• 负责人: PETER J SOUTHERN
• 金额: $ 11.53万
• 依托单位: SCRIPPS CLINIC AND RESEARCH FOUNDATION
• 依托单位国家: 美国
• 财政年份: 1987
• 资助国家: 美国
• 起止时间: 1987-07-01 至 1989-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3138622
• 关键词: DNA directed RNA polymerase; defective virus; disease /disorder model; gel electrophoresis; gene expression; genetic manipulation; immunoregulation; interfering virus; laboratory mouse; lymphocytic choriomeningitis; molecular pathology; nucleic acid hybridization; nucleic acid probes; virus RNA; virus cytopathogenic effect; virus infection mechanism

Virus infections often lead to pathogenic consequences and disease considerably beyond the acute phase on infection. The significance of persistent infections for human disease processes is only now becoming apparent. In the course of a persistent infection, disease may develop as a consequence of host immune responses against the virus and virus infected cells and/or from virus disruption of cellular functions. At present, there is only limited understanding of the molecular details of persistent virus infection. There have been many suggestions that defective interfering (DI) RNAs may be involved with the establishment and maintenance of persistent virus infections. Although DI RNAs have been linked to persistence in tissue culture systems, there is little information that relates directly to the appearance and function of DI RNAs during infection in vivo. The studies proposed here will examine persistent infections induced in laboratory mice by lymphocytic choriomeningitis virus to determine whether deleted RNAs (i.e., potential DI RNAs) appear and accumulate in persistently infected animals and whether these RNAs alter the normal course of acute infection. A complementary series of experiments will investigate potential regulatory mechanisms that reduce viral gene expression and may mediate the transition from acute to persistence infection. A detailed understanding of the molecular basis of virus persistence in one system will allow conceptual developments for the whole field of virus persistence and may suggest strategies for intervention and eventual clearance of a persistent infection.

病毒感染通常导致致病性后果， 疾病大大超过了感染的急性期。 的 持续感染对人类疾病过程的意义 现在才变得明显 在一个持续的过程中， 感染，疾病可能发展为宿主免疫的结果 针对病毒和病毒感染的细胞和/或来自 病毒破坏细胞功能。 目前只有 对持久性病毒的分子细节了解有限 感染 有许多建议，有缺陷的干扰（DI） RNA可能参与了细胞的建立和维持， 持续性病毒感染。 尽管DI RNA已经与 持久性在组织培养系统中，几乎没有信息 与DI RNA的外观和功能直接相关 在体内感染期间。 这里提出的研究将审查 小鼠淋巴细胞持续感染 脉络丛脑膜炎病毒以确定是否缺失RNA（即， 潜在的DI RNA）出现并持续积累， 感染的动物以及这些RNA是否改变了正常的过程 急性感染。 一系列补充实验将 研究减少病毒感染的潜在调节机制 基因表达，并可能介导从急性向急性的转变。 持续性感染 对病毒分子基础的详细了解 在一个系统中的持久性将允许概念发展， 病毒持久性的整个领域，并可能建议战略， 干预并最终清除持续感染。