VZV in the enteric nervous system: pathogenesis and consequences

肠神经系统中的水痘带状疱疹病毒：发病机制和后果

• 批准号: 8516884
• 负责人: MICHAEL D GERSHON
• 金额: $ 33.58万
• 依托单位: COLUMBIA UNIVERSITY HEALTH SCIENCES
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-01 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8516884
• 关键词: Afferent Neurons; Animal Model; Animals; Axon; Axonal Transport; Behavior Control; Blood; Brain; Breathing; Cavia; Cells; Chickenpox; Chickenpox Vaccine; Chronic; Coculture Techniques; Complex; Cranial Nerves; Cutaneous; Differential Diagnosis; Disease; Dorsal; Enteral; Enteric Nervous System; Enterocytes; Epithelium; Exanthema; Exocytosis; Fibroblasts; Frequencies; Functional disorder; Ganglia; Gastrointestinal Motility; Gastroparesis; Growth; Herpes zoster disease; Herpesvirus Type 3; Human; Immunity; Immunocompromised Host; Immunologic Deficiency Syndromes; In Situ; In Vitro; Individual; Infection; Infection prevention; Inflammation; Inflammatory Bowel Diseases; Injection of therapeutic agent; Intestinal Pseudo-Obstruction; Intestines; Investigation; Irritable Bowel Syndrome; Label; Life; Link; Lymphocyte; Lytic; Lytic Phase; Mus; Nerve; Nerve Block; Nerve Fibers; Neurons; Open Reading Frames; Operative Surgical Procedures; Paint; Pathogenesis; Peripheral Blood Mononuclear Cell; Phase; Proteins; Reverse Transcriptase Polymerase Chain Reaction; Route; Sensory Nerve Endings; Severities; Simplexvirus; Skin; Spinal Cord; Sympathectomy; Synapses; T-Lymphocyte; Testing; Tracer; Travel; Vesicle; Viral; Viral Proteins; Viremia; Virion; Virus; Virus Diseases; Virus Latency; Viscera; afferent nerve; base; design; experience; immunocytochemistry; in vitro Model; in vivo; intradermal injection; keratinocyte; killings; late endosome; latent infection; man; mutant; particle; preference; protein expression; research study; secondary infection; spinal nerve posterior root; true blue; viral DNA; visceral afferent nerve

DESCRIPTION (provided by applicant): The enteric nervous system (ENS) can control the behavior of the bowel without input from brain or spinal cord. A functioning ENS is essential for life and, when abnormal, causes discomfort and may contribute to the pathophysiology or severity of disorders of gastrointestinal motility, secretion, and inflammation. We have recently discovered that varicella zoster virus (VZV) establishes latency within human enteric neurons in most individuals who have experienced natural varicella or received varicella vaccine. VZV, moreover, has been linked to the occurrence of lethal pseudoobstruction in immunocompromised individuals. Neither the route by which VZV gains access to the ENS, nor the frequency or consequences of its reactivation in enteric neurons ("enteric zoster") has previously been explored. The current proposal is designed to test the hypotheses that transport in visceral afferent nerves conducts VZV to the ENS, that cell- free virions establish latency in enteric neurons, and that the non-structural VZV ORF61 protein must be expressed in neurons to enable VZV to manifest lytic infection or to reactivate from latency. Although VZV displays a marked preference for human cells, we have developed animal models that permit VZV infection of the ENS to be studied in vitro and in vivo. Depending on conditions, VZV recapitulates latent, lytic, and reactivating infection in enteric neurons isolated from guinea pigs or mice and, when introduced to the bowel, VZV establishes latency in the guinea pig ENS in situ. The proposal has 3 specific aims: (1) Can VZV travel from the skin to the ENS in sensory nerve fibers? Preliminary studies have identified neurons in dorsal route ganglia that project both to skin and gut. We will determine whether latent infection is established in the ENS when VZV is introduced to the skin and whether VZV-infected nerve terminals release infectious cell-free VZV that crosses synaptic gaps to transfer latent infection to target neurons. (2) Can a viremia establish latent VZV infection of enteric neurons? We will determine whether VZV-infected T lymphocytes release infectious cell-free VZV and whether they can establish latency directly in enteric neurons or indirectly via infections of the mucosal epithelium or skin. Preliminary studies have shown that VZV DNA is present in guinea pig enteric neurons following the iv injection of VZV-infected peripheral blood mononuclear cells. (3) Is VZV ORF61 protein expression necessary for the manifestation of lytic infection in enteric neurons? We will study the ability of a VZV mutant that lacks ORF61 to establish lytic infection of enteric neurons or reactivate from latency. The significance of understanding VZV infection of the ENS is enhanced by the possibility that unsuspected reactivation of VZV in enteric neurons might contribute to the pathogenesis of GI disorders such as irritable bowel syndrome, inflammatory bowel disease, idiopathic gastroparesis, and chronic intestinal pseudoobstruction.

描述(申请人提供)：肠道神经系统(ENS)可以控制肠道的行为，而不需要大脑或脊髓的输入。正常的ENS对生命是必不可少的，当异常时，会导致不适，并可能导致胃肠动力、分泌和炎症的病理生理或严重障碍。我们最近发现，水痘带状疱疹病毒(VZV)在经历过自然水痘或接受水痘疫苗接种的大多数人的肠神经元内建立潜伏期。此外，VZV与免疫受损个体发生致死性假性梗阻有关。无论是VZV进入ENS的途径，还是它在肠道神经元(“肠带状带”)重新激活的频率或后果，以前都没有被探索过。目前的提议旨在测试以下假设：内脏传入神经中的运输将VZV传导到ENS，无细胞病毒粒子在肠道神经元中建立潜伏期，以及VZV ORF61蛋白必须在神经元中表达，才能使VZV表现出裂解性感染或从潜伏期重新激活。尽管VZV表现出明显的对人类细胞的偏好，但我们已经开发出允许VZV感染ENS的动物模型，以便在体外和体内进行研究。根据不同的条件，VZV在从豚鼠或小鼠分离的肠道神经元中重现潜伏的、溶解的和重新激活的感染，当被引入肠道时，VZV在豚鼠的ENS中原位建立潜伏期。该提案有3个具体目标：(1)VZV能否通过感觉神经纤维从皮肤传播到ENS？初步研究发现，背路神经节中的神经元既投射到皮肤，也投射到肠道。我们将确定当VZV被引入皮肤时是否在ENS中建立潜伏感染，以及VZV感染的神经末梢是否释放感染细胞的VZV穿过突触间隙将潜伏感染转移到靶神经元。(2)病毒血症能否建立肠道神经元的潜伏性VZV感染？我们将确定感染VZV的T淋巴细胞是否释放感染性的无细胞VZV，以及它们是否可以直接在肠神经细胞中建立潜伏期，或者通过感染粘膜上皮或皮肤间接建立潜伏期。初步研究表明，静脉注射VZV感染的外周血单个核细胞后，豚鼠肠神经细胞中存在VZV DNA。(3)VZV ORF61蛋白的表达是否是肠道神经元溶血性感染的必要表现？我们将研究缺乏ORF61的VZV突变体建立肠道神经元裂解感染或从潜伏期重新激活的能力。VZV在肠道神经元的意外激活可能参与了肠易激综合征、炎症性肠病、特发性胃轻瘫和慢性假性肠梗阻等胃肠道疾病的发病机制，这加强了了解VZV感染ENS的重要性。