Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA
J Virol. 2020 Feb 14;94(5). doi: 10.1128/JVI.01522-19.
The encode many conserved genes, including the conserved herpesvirus protein kinase (CHPK) that has multifunctional properties. In most cases, herpesviruses lacking CHPK can propagate in cell culture to various degrees, depending on the virus and cell culture system. However, in the natural animal model system of Marek's disease alphaherpesvirus (MDV) in chickens, CHPK is absolutely required for interindividual spread from chicken to chicken. The lack of biological reagents for chicken and MDV has limited our understanding of this important gene during interindividual spread. Here, we engineered epitope-tagged proteins in the context of virus infection in order to detect CHPK in the host. Using immunofluorescence assays and Western blotting during infection in cell culture and in chickens, we determined that the invariant lysine 170 (K170) of MDV CHPK is required for interindividual spread and autophosphorylation of CHPK and that mutation to methionine (M170) results in instability of the CHPK protein. Using these newly generated viruses allowed us to examine the expression of CHPK in infected chickens, and these results showed that mutant CHPK localization and late viral protein expression were severely affected in feather follicles wherein MDV is shed, providing important information on the requirement of CHPK for interindividual spread. Marek's disease in chickens is caused by 2, better known as Marek's disease alphaherpesvirus (MDV). Current vaccines only reduce tumor formation but do not block interindividual spread from chicken to chicken. Understanding MDV interindividual spread provides important information for the development of potential therapies to protect against Marek's disease while also providing a reliable natural host in order to study herpesvirus replication and pathogenesis in animals. Here, we studied the conserved protein kinase (CHPK) in cell culture and during infection in chickens. We determined that MDV CHPK is not required for cell-to-cell spread, for disease induction, and for oncogenicity. However, it is required for interindividual spread, and mutation of the invariant lysine (K170) results in stability issues and aberrant expression in chickens. This study is important because it addresses the critical role CHPK orthologs play in the natural host.
该病毒编码许多保守基因,包括具有多功能特性的保守疱疹病毒蛋白激酶(CHPK)。在大多数情况下,缺乏 CHPK 的疱疹病毒可以在细胞培养中以不同程度进行繁殖,具体取决于病毒和细胞培养系统。然而,在天然的马立克氏病 alphaherpesvirus(MDV)鸡动物模型系统中,CHPK 绝对是病毒在鸡与鸡之间个体间传播所必需的。缺乏鸡和 MDV 的生物试剂限制了我们对这个在个体间传播过程中重要基因的理解。在这里,我们在病毒感染的背景下构建了表位标记蛋白,以便在宿主中检测 CHPK。通过细胞培养和鸡感染中的免疫荧光检测和 Western blot 分析,我们确定 MDV CHPK 的不变赖氨酸 170(K170)对于个体间传播以及 CHPK 的自身磷酸化是必需的,并且突变为蛋氨酸(M170)会导致 CHPK 蛋白的不稳定。利用这些新生成的病毒,我们可以检查感染鸡中 CHPK 的表达,这些结果表明,突变的 CHPK 定位和晚期病毒蛋白表达在羽毛滤泡中受到严重影响,而羽毛滤泡是 MDV 脱落的地方,这为 CHPK 对于个体间传播的必要性提供了重要信息。鸡马立克氏病是由 2 引起的,也称为马立克氏病 alphaherpesvirus(MDV)。目前的疫苗只能减少肿瘤的形成,但不能阻止鸡与鸡之间的个体间传播。了解 MDV 个体间传播为开发潜在的治疗方法提供了重要信息,以防止马立克氏病,同时为研究疱疹病毒在动物中的复制和发病机制提供了可靠的天然宿主。在这里,我们在细胞培养和鸡感染中研究了保守的 蛋白激酶(CHPK)。我们确定 MDV CHPK 对于细胞间传播、疾病诱导和致癌性不是必需的。然而,它对于个体间传播是必需的,并且不变赖氨酸(K170)的突变会导致稳定性问题和在鸡中的异常表达。这项研究很重要,因为它解决了 CHPK 同源物在天然宿主中所起的关键作用。