Defining the determinants on the alphavirus receptor NRAMP required for virus bin

定义病毒箱所需的甲病毒受体 NRAMP 的决定因素

• 批准号: 8606813
• 负责人: Sara Cherry
• 金额: $ 20万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-02-01 至 2016-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8606813
• 关键词: Accounting; Acute; Adult; Alleles; Alphavirus; Alphavirus Infections; Antiviral Agents; Arboviruses; Arthritis; Automobile Driving; Binding; Biochemical; Biological Assay; Categories; Cell Surface Receptors; Cell membrane; Cell surface; Cells; Chikungunya virus; Chronic; Clathrin; Culicidae; Development; Disease; Drosophila genus; Encephalitis; Endocytosis; Genes; Genetic Polymorphism; Glycoproteins; Goals; Grant; Homologous Gene; Human; Infection; Insecta; Integration Host Factors; Iron; Knowledge; Mammalian Cell; Mammals; Mediating; Modeling; Mutation; Nature; Nramp protein; Pathogenesis; Pathway interactions; Play; Polyarthralgias; Predisposition; Protein Binding; RNA Interference; Rodent; Role; Ross river virus; Seroprevalences; Severity of illness; Signal Transduction; Sindbis Virus; Structure; Technology; Testing; Texas; Therapeutic; Tropism; Vaccines; Variant; Venezuelan Equine Encephalitis Virus; Vertebrates; Viral; Viral Pathogenesis; Virus; Virus Diseases; Virus Receptors; alphavirus receptor; biodefense; combat; enzootic; epizootic; fly; genome wide association study; genome-wide; human disease; pathogen; public health relevance; receptor; therapeutic development; trafficking; transmission process

DESCRIPTION (provided by applicant): Alphavirus interactions with cellular receptors are likely to play a major role determining viral tropism and driving virus-induced disease. However, the viral receptors that mediate alphavirus entry are poorly understood. A genome wide screen using Sindbis virus identified NRAMP as a potential alphavirus entry receptor in insect cells. Additional studies suggest that NRAMP is also an entry receptor for Venezuelan Equine Encephalitis virus. Furthermore, in mammalian cells the ubiquitously expressed homolog, NRAMP2, can mediate infection of these alphaviruses. Our long-term goal is to dissect the role of NRAMPs in infectivity and pathogenesis of alphaviruses with the goal of developing strategies to combat these pathogens. We will study this important interaction by dissecting the determinants on NRAMPs that mediate binding and entry. Furthermore, we will sequence NRAMP from different enzootic and epizootic hosts to determine whether polymorphisms impact virus infection. We will take advantage of powerful assays that we have developed to study alphavirus entry and infection both in insect and mammalian cells to explore the role of NRAMPs in viral infection. Our central hypothesis is that dissecting the interactions of these medically important arboviruses with their receptor will reveal mechanisms that will aid in the development of antiviral treatments against these understudied pathogens for which there are no vaccines or therapeutics.

描述（由申请方提供）：甲病毒与细胞受体的相互作用可能在决定病毒嗜性和驱动病毒诱导的疾病中发挥主要作用。 然而，介导甲病毒进入的病毒受体知之甚少。 使用辛德毕斯病毒的全基因组筛选将NRAMP鉴定为昆虫细胞中潜在的甲病毒进入受体。 其他研究表明，NRAMP也是委内瑞拉马脑炎病毒的进入受体。此外，在哺乳动物细胞中，普遍表达的同源物NRAMP2可以介导这些甲病毒的感染。 我们的长期目标是剖析NRAMP在甲病毒感染性和发病机制中的作用，目的是制定对抗这些病原体的策略。 我们将研究这一重要的相互作用，解剖的决定因素对NRAMP介导的结合和进入。此外，我们将对来自不同地方病和流行病宿主的NRAMP进行测序，以确定多态性是否影响病毒感染。我们将利用我们已经开发的用于研究甲病毒在昆虫和哺乳动物细胞中的进入和感染的强大测定来探索NRAMP在病毒感染中的作用。我们的中心假设是，解剖这些医学上重要的虫媒病毒与其受体的相互作用将揭示机制，这将有助于开发针对这些未充分研究的病原体的抗病毒治疗，这些病原体没有疫苗或治疗方法。