Liao Yifei, Fang Xin, Ai-Mahmood Mohammad, Li Qinglei, Lupiani Blanca, Reddy Sanjay M
Department of Veterinary Pathobiology, College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, TX 77843, USA.
Department of Veterinary Integrative Biosciences, College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, TX 77843, USA.
Microorganisms. 2021 Apr 9;9(4):785. doi: 10.3390/microorganisms9040785.
2 (GaHV-2), commonly known as Marek's disease virus type 1 (MDV-1), is an oncogenic avian alphaherpesvirus, and along with its close relatives- 3 (GaHV-3) or MDV-2 and 1 (MeHV-1) or turkey herpesvirus (HVT)-belongs to the genus. We and others previously showed that MDV-1 U3 protein kinase plays an important role in viral replication and pathogenesis, which could be partially compensated by MDV-2 and HVT U3. In this study, we further studied the differential roles of MDV-1, MDV-2 and HVT U3 in regulating viral gene expression and replication. Our results showed that MDV-2 and HVT U3 could differentially compensate MDV-1 U3 regulation of viral gene expression in vitro. MDV-2 and HVT U3 could also partially rescue the replication deficiency of MDV-1 U3 null virus in the spleen and thymus, as determined by immunohistochemistry analysis of MDV-1 pp38 protein. Importantly, using immunohistochemistry and dual immunofluorescence assays, we found that MDV-2 U3, but not HVT U3, fully compensated MDV-1 U3 regulation of MDV-1 replication in bursal B lymphocytes. In conclusion, our study provides the first comparative analysis of U3 from MDV-1, MDV-2 and HVT in regulating viral gene expression in cell culture and MDV-1 replication in lymphocytes.
2型禽疱疹病毒(GaHV-2),通常称为1型马立克氏病病毒(MDV-1),是一种致癌性禽α疱疹病毒,与其近亲——3型禽疱疹病毒(GaHV-3)或MDV-2以及1型马立克氏病病毒(MeHV-1)或火鸡疱疹病毒(HVT)——同属一个属。我们和其他人之前表明,MDV-1 U3蛋白激酶在病毒复制和发病机制中起重要作用,MDV-2和HVT U3可部分补偿该作用。在本研究中,我们进一步研究了MDV-1、MDV-2和HVT U3在调节病毒基因表达和复制中的不同作用。我们的结果表明,MDV-2和HVT U3在体外可不同程度地补偿MDV-1 U3对病毒基因表达的调节。通过对MDV-1 pp38蛋白的免疫组织化学分析确定,MDV-2和HVT U3也可部分挽救MDV-1 U3缺失病毒在脾脏和胸腺中的复制缺陷。重要的是,通过免疫组织化学和双重免疫荧光测定,我们发现MDV-2 U3而非HVT U3可完全补偿MDV-1 U3对法氏囊B淋巴细胞中MDV-1复制的调节。总之,我们的研究首次对MDV-1、MDV-2和HVT的U3在调节细胞培养中的病毒基因表达和淋巴细胞中的MDV-1复制方面进行了比较分析。