Department of Comparative Physiology, Uppsala University, Uppsala, Sweden.
Department of Veterinary Technology, Faculty of Veterinary Technology, Kasetsart University, Bangkok, Thailand.
J Virol. 2014 Jul;88(14):8116-28. doi: 10.1128/JVI.01014-14. Epub 2014 May 7.
We have previously shown that multifunctional calreticulin (CRT), which resides in the endoplasmic reticulum (ER) and is involved in ER-associated protein processing, responds to infection with white spot syndrome virus (WSSV) by increasing mRNA and protein expression and by forming a complex with gC1qR and thereby delaying apoptosis. Here, we show that CRT can directly interact with WSSV structural proteins, including VP15 and VP28, during an early stage of virus infection. The binding of VP28 with CRT does not promote WSSV entry, and CRT-VP15 interaction was detected in the viral genome in virally infected host cells and thus may have an effect on WSSV replication. Moreover, CRT was detected in the viral envelope of purified WSSV virions. CRT was also found to be of high importance for proper oligomerization of the viral structural proteins VP26 and VP28, and when CRT glycosylation was blocked with tunicamycin, a significant decrease in both viral replication and assembly was detected. Together, these findings suggest that CRT confers several advantages to WSSV, from the initial steps of WSSV infection to the assembly of virions. Therefore, CRT is required as a "vital factor" and is hijacked by WSSV for its replication cycle. Importance: White spot syndrome virus (WSSV) is a double-stranded DNA virus and the cause of a serious disease in a wide range of crustaceans that often leads to high mortality rates. We have previously shown that the protein calreticulin (CRT), which resides in the endoplasmic reticulum (ER) of the cell, is important in the host response to the virus. In this report, we show that the virus uses this host protein to enter the cell and to make the host produce new viral structural proteins. Through its interaction with two viral proteins, the virus "hijacks" host calreticulin and uses it for its own needs. These findings provide new insight into the interaction between a large DNA virus and the host protein CRT and may help in understanding the viral infection process in general.
我们之前已经表明,驻留在内质网 (ER) 中的多功能钙网蛋白 (CRT) 参与 ER 相关蛋白加工,通过增加 mRNA 和蛋白质表达并与 gC1qR 形成复合物来响应白斑综合征病毒 (WSSV) 的感染,从而延迟细胞凋亡。在这里,我们表明 CRT 可以在病毒感染的早期阶段直接与 WSSV 结构蛋白(包括 VP15 和 VP28)相互作用。VP28 与 CRT 的结合不会促进 WSSV 的进入,并且在病毒感染的宿主细胞中的病毒基因组中检测到 CRT-VP15 相互作用,因此可能对 WSSV 的复制产生影响。此外,在纯化的 WSSV 病毒粒子的病毒包膜中检测到 CRT。CRT 对于病毒结构蛋白 VP26 和 VP28 的正确寡聚化也非常重要,并且当用衣霉素阻断 CRT 糖基化时,检测到病毒复制和组装均显著减少。总之,这些发现表明 CRT 为 WSSV 提供了多种优势,从 WSSV 感染的初始步骤到病毒粒子的组装。因此,CRT 是必需的“重要因素”,并且被 WSSV 劫持用于其复制周期。
白斑综合征病毒 (WSSV) 是一种双链 DNA 病毒,是广泛甲壳类动物的一种严重疾病的病原体,通常导致高死亡率。我们之前已经表明,驻留在细胞内质网 (ER) 中的钙网蛋白 (CRT) 蛋白在宿主对病毒的反应中很重要。在本报告中,我们表明病毒利用这种宿主蛋白进入细胞并使宿主产生新的病毒结构蛋白。通过与两种病毒蛋白的相互作用,病毒“劫持”宿主钙网蛋白并将其用于自身需要。这些发现为大型 DNA 病毒与宿主蛋白 CRT 之间的相互作用提供了新的见解,并可能有助于一般理解病毒感染过程。