Viral and host responses to HSV infection

描述（由申请人提供）：单纯疱疹病毒（HSV）是一种常见和重要的病原体，可引起人类多种疾病过程，从感冒和生殖器溃疡到失明。单纯疱疹病毒的生命周期有两个不同的阶段：溶解性感染和潜伏性感染。在决定溶解性感染和潜伏性感染之间转换的关键HSV蛋白是感染细胞蛋白0 （ICP0）。ICP0是一种分子量为110 kda的核磷酸化蛋白，它能强烈激活病毒基因表达，降解核结构域（ND） 10中的细胞蛋白，并抑制细胞干扰素（ifn）的抗病毒反应。ifn是分泌的细胞免疫调节因子，可上调nd10相关蛋白的表达，以限制病毒的传播和复制。遗传学研究表明，nd10相关蛋白早幼粒细胞白血病（PML）在ifn介导的HSV复制抑制中起重要作用。因此，ICP0、PML和ifn之间的相互作用很可能决定了HSV感染的类型。病毒宿主通过干扰素对感染产生应答所需的ICP0和PML的机制和结构域在很大程度上尚未确定。我们研究的长期目标是在分子水平上了解病毒-细胞相互作用如何影响HSV感染。本提案的目的是确定ICP0和PML上的特定基序如何调节病毒-宿主反应。我们的中心假设是ICP0损害了PML的抗病毒活性，而这反过来又是有效的病毒复制所必需的。为了验证这一假设，我们将使用多种遗传、生化和细胞生物学技术来鉴定ICP0和PML上参与调节HSV复制的基序。我们的研究结果有望导致新的抗病毒疗法，抑制或限制HSV疾病的严重程度。为此，我们的三个特定目标是：1)确定PML基序在IFN对HSV感染的反应中的作用；2)确定ICP0中的结构域和ICP0上的位点，这些结构域有助于抵抗宿主对感染的防御；3)确定ICP0-PML相互作用在调节细胞抗病毒反应中的作用。这项研究的公共卫生相关性在于，HSV感染是西方工业化国家传染性失明的主要原因。从这些研究中，我们期望确定和表征HSV （ICP0）与其宿主（IFN和PML）之间的关键联系，这些联系决定了HSV将建立的感染类型。这些结果可能用于开发新的抗hsv治疗方法。

DESCRIPTION (provided by applicant): Herpes simplex virus (HSV) is a common and significant pathogen which causes a variety of disease processes in humans, ranging from cold and genital sores to blindness. The lifecycle of HSV has two distinct phases: lytic and latent infections. A pivotal HSV protein in determining the switch between lytic and latent infections is infected cell protein 0 (ICP0). ICP0 is a 110-KDa nuclear phosphoprotein that strongly transactivates viral gene expression, degrades cellular proteins in nuclear domain (ND) 10, and inhibits the anti-viral response of cellular interferons (IFNs). IFNs are secreted cellular immunomodulatory factors that upregulate the expression of ND10-associated proteins to limit the spread and replication of viruses. Genetics studies have indicated that the ND10-associated protein, promyelocytic leukemia (PML), plays an important role in IFN-mediated inhibition of HSV replication. Thus, it is likely that the interactions between ICP0, PML, and IFNs govern the type of infection HSV will establish. The mechanisms and domains on ICP0 and PML required in virus-host responses to infection through IFNs have been largely undetermined. The long-term objective of our studies is to understand at the molecular level how virus-cell interactions affect HSV infection. The objective of this proposal is to determine how specific motifs on ICP0 and PML modulate the virus-host response. Our central hypothesis is that ICP0 impairs the anti-viral activity of PML, which, in turn, is required for efficient viral replication. To test this hypothesis, we will use a variety of genetic, biochemical, and cell biology techniques to identify motifs on ICP0 and PML that participate in regulating HSV replication. Results from our studies are expected to lead to novel anti-viral therapies that inhibit or limit the severity of HSV diseases. For this purpose, our three Specific Aims are to: 1) Determine the contribution of PML motifs in the IFN response to HSV infection, 2) Identify domains in and sites on ICP0 that serve to counteract host defenses to infection, and 3) Determine the role of ICP0-PML interactions in modulating the cellular anti-viral response. The public health relevance of this research is that HSV infections are the primary cause of infectious blindness in western industrialized countries. From these studies, we expect to identify and characterize crucial connections between HSV (ICP0) and its host (IFN and PML) that determine the type infection HSV will establish. These results may be used to develop novel anti-HSV treatments.