Graduate Institute of Microbiology, College of Medicine, National Taiwan University, Taipei, Taiwan.
J Virol. 2014 May;88(9):4962-75. doi: 10.1128/JVI.00063-14. Epub 2014 Feb 19.
Epstein-Barr virus (EBV) lytic replication involves complex processes, including DNA synthesis, DNA cleavage and packaging, and virion egress. These processes require many different lytic gene products, but the mechanisms of their actions remain unclear, especially for DNA cleavage and packaging. According to sequence homology analysis, EBV BALF3, encoded by the third leftward open reading frame of the BamHI-A fragment in the viral genome, is a homologue of herpes simplex virus type 1 UL28. This gene product is believed to possess the properties of a terminase, such as nucleolytic activity on newly synthesized viral DNA and translocation of unit length viral genomes into procapsids. In order to characterize EBV BALF3, the protein was produced by and purified from recombinant baculoviruses and examined in an enzymatic reaction in vitro, which determined that EBV BALF3 acts as an endonuclease and its activity is modulated by Mg(2+), Mn(2+), and ATP. Moreover, in EBV-positive epithelial cells, BALF3 was expressed and transported from the cytoplasm into the nucleus following induction of the lytic cycle, and gene silencing of BALF3 caused a reduction of DNA packaging and virion release. Interestingly, suppression of BALF3 expression also decreased the efficiency of DNA synthesis. On the basis of these results, we suggest that EBV BALF3 is involved simultaneously in DNA synthesis and packaging and is required for the production of mature virions.
Virus lytic replication is essential to produce infectious virions, which is responsible for virus survival and spread. This work shows that an uncharacterized gene product of the human herpesvirus Epstein-Barr virus (EBV), BALF3, is expressed during the lytic cycle. In addition, BALF3 mediates an endonucleolytic reaction and is involved in viral DNA synthesis and packaging, leading to influence on the production of mature virions. According to sequence homology and physical properties, the lytic gene product BALF3 is considered a terminase in EBV. These findings identify a novel viral gene with an important role in contributing to a better understanding of the EBV life cycle.
Epstein-Barr 病毒(EBV)裂解复制涉及复杂的过程,包括 DNA 合成、DNA 切割和包装以及病毒粒子出芽。这些过程需要许多不同的裂解基因产物,但它们的作用机制仍不清楚,特别是对于 DNA 切割和包装。根据序列同源性分析,EBV BALF3 是病毒基因组 BamHI-A 片段中第三个左向开放阅读框编码的产物,是单纯疱疹病毒 1 UL28 的同源物。该基因产物被认为具有末端酶的特性,例如对新合成的病毒 DNA 具有核酶活性,并且将单位长度的病毒基因组转运到前衣壳中。为了表征 EBV BALF3,该蛋白由重组杆状病毒产生和纯化,并在体外酶反应中进行了检查,结果确定 EBV BALF3 作为内切核酸酶起作用,其活性受 Mg2+、Mn2+ 和 ATP 调节。此外,在 EBV 阳性上皮细胞中,在诱导裂解周期后,BALF3 从细胞质中表达并转运到细胞核中,并且 BALF3 的基因沉默导致 DNA 包装和病毒粒子释放减少。有趣的是,抑制 BALF3 表达也降低了 DNA 合成的效率。基于这些结果,我们认为 EBV BALF3 同时参与 DNA 合成和包装,并需要产生成熟的病毒粒子。
病毒裂解复制对于产生感染性病毒粒子至关重要,这是病毒存活和传播的原因。这项工作表明,人类疱疹病毒 Epstein-Barr 病毒(EBV)的未表征基因产物 BALF3 在裂解周期中表达。此外,BALF3 介导内切核酸酶反应,并参与病毒 DNA 合成和包装,从而影响成熟病毒粒子的产生。根据序列同源性和物理性质,裂解基因产物 BALF3 被认为是 EBV 中的末端酶。这些发现确定了一种新的病毒基因,该基因在更好地理解 EBV 生命周期方面具有重要作用。