Kumar Pankaj, van den Hurk Jan, Ayalew Lisanework E, Gaba Amit, Tikoo Suresh K
Vaccine and Infectious Disease Organization -International Vaccine Center (VIDO- InterVac1), University of Saskatchewan, Saskatoon, S7N 5E3, SK, Canada.
Vaccinology & Immunotherapeutics program, School of Public Health, University of Saskatchewan, Saskatoon, S7N 5E5, SK, Canada.
Vet Res. 2015 Jul 9;46(1):79. doi: 10.1186/s13567-015-0214-z.
Turkey adenovirus 3 (TAdV-3) causes high mortality and significant economic losses to the turkey industry. However, little is known about the molecular determinants required for viral replication and pathogenesis. Moreover, TAdV-3 does not grow well in cell culture, thus detailed structural studies of the infectious particle is particularly challenging. To develop a better understanding of virus-host interactions, we performed a comprehensive proteomic analysis of proteinase K treated purified TAdV-3 virions isolated from spleens of infected turkeys, by utilizing one-dimensional liquid chromatography mass spectrometry. Our analysis resulted in the identification of 13 viral proteins associated with TAdV-3 virions including a novel uncharacterized TaV3gp04 protein. Further, we detected 18 host proteins in purified virions, many of which are involved in cell-to cell spread, cytoskeleton dynamics and virus replication. Notably, seven of these host proteins have not yet been reported to be present in any other purified virus. In addition, five of these proteins are known antiviral host restriction factors. The availability of reagents allowed us to identify two cellular proteins (collagen alpha-1 (VI) chain and haemoglobin) in the purified TAdV-3 preparations. These results represent the first comprehensive proteomic profile of TAdV-3 and may provide information for illustrating TAdV-3 replication and pathogenesis.
土耳其腺病毒3型(TAdV-3)给火鸡养殖业造成了高死亡率和重大经济损失。然而,对于病毒复制和发病机制所需的分子决定因素,我们却知之甚少。此外,TAdV-3在细胞培养中生长不佳,因此对感染性颗粒进行详细的结构研究极具挑战性。为了更好地理解病毒与宿主的相互作用,我们利用一维液相色谱质谱法,对从感染火鸡脾脏中分离出的经蛋白酶K处理的纯化TAdV-3病毒粒子进行了全面的蛋白质组学分析。我们的分析鉴定出了13种与TAdV-3病毒粒子相关的病毒蛋白,其中包括一种新的未鉴定的TaV3gp04蛋白。此外,我们在纯化的病毒粒子中检测到了18种宿主蛋白,其中许多蛋白参与细胞间传播、细胞骨架动态变化和病毒复制。值得注意的是,这些宿主蛋白中有7种尚未被报道存在于任何其他纯化病毒中。此外,这些蛋白中有5种是已知的抗病毒宿主限制因子。现有试剂使我们能够在纯化的TAdV-3制剂中鉴定出两种细胞蛋白(胶原蛋白α-1(VI)链和血红蛋白)。这些结果代表了TAdV-3的首个全面蛋白质组概况,可能为阐明TAdV-3的复制和发病机制提供信息。