Genetic determinants of HSV-1 virulence in neurons

HSV-1 神经元毒力的遗传决定因素

• 批准号: 8165606
• 负责人: MORIAH SZPARA
• 金额: $ 15万
• 依托单位: PENNSYLVANIA STATE UNIVERSITY, THE
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-06-17 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8165606
• 关键词: Affect; Award; Bioinformatics; Biological; Biological Models; Blindness; Cells; Clinical; Data; Disease; Encephalitis; Foundations; Funding; Future; Genetic; Genetic Determinism; Genome; Genotype; Goals; Herpesvirus 1; Human; Human Virus; Immunology; Infection; Integration Host Factors; Laboratory Research; Lead; Light; Link; Maps; Molecular; Mus; Nervous system structure; Neurobiology; Neurons; Patients; Peripheral; Phenotype; Publications; Recombinants; Research; Research Project Grants; Research Proposals; Symptoms; Testing; Time; Training; United States; Viral; Viral Encephalitis; Viral Genes; Viral Physiology; Virulence; Virulent; Virus; base; career; career development; combat; comparative genomics; genome sequencing; grasp; in vivo; in vivo Model; mouse model; neurotropic; neurovirulence; pathogen; post-doctoral training; recombinant virus; therapeutic target; virology

DESCRIPTION (provided by applicant): My career goal is to establish an academic research laboratory devoted to understanding how pathogens affect the nervous system, and what features of neurons could provide useful therapeutic targets to combat these infections. I am well-prepared to contribute significantly to our understanding of neurotropic pathogens, based on the strong foundations of my graduate training in neurobiology and postdoctoral training in virology. This award will facilitate my career development by allowing me to gain training in bioinformatics and immunology, and also by providing funding and time to generate data and publications to facilitate a future R01 application. The overall goal of this research proposal is to understand how pathogens interact with the host nervous system, specifically to grasp what genetic features can make a neurotropic pathogen more or less virulent. Herpes simplex virus 1 (HSV-1) is a widespread human pathogen that establishes latency in human peripheral neurons and reactivates repeatedly throughout a patient's lifetime. HSV-1 is a leading cause of infectious blindness in the United States, and the main cause of sporadic, fatal encephalitis. It is unknown why certain HSV-1 infections progress to the level of encephalitis, but it is almost certainly influenced by both viral and host factors. Mouse models of this disease have demonstrated that viral strains differ in their virulence and ability to cause encephalitis. However the ability to map these phenotypic differences to specific viral genes has been limited by the lack of comparative genomic information about this virus - only one wild type HSV-1 genome has been known for the last two decades. I recently demonstrated that high-throughput sequencing (HTS) and bioinformatic assembly can be used to obtain further HSV-1 genomes. I propose to use HTS to test this hypothesis: that genetic loci which are enriched in neurovirulent strains, and lacking in strains that do not cause encephalitis in mice, are highly likely to be causally associated with the neurovirulence phenotype. To achieve this, my specific aims are: (1) to use HTS, genome assembly, & bioinformatic comparison of diverse clinical isolates of HSV-1, to find loci that are enriched in highly neurovirulent strains versus non-virulent ones; and (2) to generate viral recombinants, by either adding or removing putative neurovirulence loci, and test for associated changes in phenotype using an in vivo model of viral encephalitis. These aims will lead to future research directions, using standard molecular and cell biological approaches to explore how these neurovirulence loci affect neuronal function and the viral infectious cycle. This proposal will shed light on mechanisms of neurovirulence in this pervasive human virus, and highlight aspects of virulence to consider in other neurotropic pathogens. NARRATIVE: Herpes simplex virus 1 (HSV-1) is a widespread human virus. This research will investigate how HSV-1 virus isolated from one patient may differ from that of another. This will help us understand why some patients suffer more severe symptoms from HSV-1 infection than others.

描述(申请人提供)：我的职业目标是建立一个学术研究实验室，致力于了解病原体如何影响神经系统，以及神经元的哪些特征可以提供有用的治疗靶点来对抗这些感染。基于我的神经生物学研究生培训和病毒学博士后培训的坚实基础，我已经做好了充分的准备，为我们对神经性病原体的理解做出重大贡献。这项奖励将通过允许我获得生物信息学和免疫学方面的培训来促进我的职业发展，并通过提供资金和时间来生成数据和出版物，以促进未来的R01应用。这项研究计划的总体目标是了解病原体如何与宿主神经系统相互作用，特别是掌握哪些遗传特征可以使嗜神经病原体的毒力增强或减弱。单纯疱疹病毒1型(HSV-1)是一种广泛存在的人类病原体，它在人类周围神经元中建立潜伏期，并在患者的一生中反复激活。HSV-1是美国传染性失明的主要原因，也是散发性、致命性脑炎的主要原因。目前尚不清楚为什么某些HSV-1感染会发展到脑炎的程度，但几乎可以肯定的是，它受到病毒和宿主因素的影响。这种疾病的小鼠模型已经证明，病毒株的毒力和引起脑炎的能力不同。然而，由于缺乏关于这种病毒的比较基因组信息，将这些表型差异映射到特定病毒基因的能力一直受到限制--在过去的20年里，只有一个野生型HSV-1基因组已知。我最近证明，高通量测序(HTS)和生物信息学组装可以用来获得更多的HSV-1基因组。我建议使用HTS来检验这一假设：富含神经毒力菌株的遗传位点，以及缺乏不会导致小鼠脑炎的菌株，极有可能与神经毒力表型存在因果关系。为此，我的具体目标是：(1)利用HTS、基因组组装和生物信息学对不同的HSV-1临床毒株进行比较，找到富含高神经毒力毒株与非强毒毒株的基因座；以及(2)通过添加或移除可能的神经毒力基因座来产生病毒重组体，并利用病毒性脑炎的体内模型测试相关的表型变化。这些目标将引领未来的研究方向，使用标准的分子和细胞生物学方法来探索这些神经毒力基因座如何影响神经功能和病毒感染周期。这项建议将阐明这种普遍存在的人类病毒的神经毒力机制，并强调在其他嗜神经病原体中需要考虑的毒力方面。 简介：单纯疱疹病毒1型(HSV-1)是一种广泛传播的人类病毒。这项研究将调查从一个患者身上分离的HSV-1病毒与从另一个患者身上分离的HSV-1病毒有何不同。这将有助于我们了解为什么一些患者感染HSV-1的症状比其他患者更严重。