Torres Lilith, Tang Qiyi
Department of Microbiology, Ponce Health Sciences University, Ponce Research Institute, Ponce, PR, 00716, USA.
Virol Sin. 2014 Dec;29(6):343-52. doi: 10.1007/s12250-014-3532-9. Epub 2014 Nov 25.
Three crucial hurdles hinder studies on human cytomegalovirus (HCMV): strict species specificity, differences between in vivo and in vitro infection, and the complexity of gene regulation. Ever since the sequencing of the whole genome was first accomplished, functional studies on individual genes have been the mainstream in the CMV field. Gene regulation has therefore been elucidated in a more detailed fashion. However, viral gene regulation is largely controlled by both cellular and viral components. In other words, viral gene expression is determined by the virus-host interaction. Generally, cells respond to viral infection in a defensive pattern; at the same time, viruses try to counteract the cellular defense or else hide in the host (latency). Viruses evolve effective strategies against cellular defense in order to achieve replicative success. Whether or not they are successful, cellular defenses remain in the whole viral replication cycle: entry, immediate-early (IE) gene expression, early gene expression, DNA replication, late gene expression, and viral egress. Many viral strategies against cellular defense, and which occur in the immediate-early time of viral infection, have been documented. In this review, we will summarize the documented biological functions of IE1 and pp71 proteins, especially with regard to how they counteract cellular intrinsic defenses.
三个关键障碍阻碍了对人类巨细胞病毒(HCMV)的研究:严格的物种特异性、体内感染与体外感染的差异以及基因调控的复杂性。自从首次完成全基因组测序以来,对单个基因的功能研究一直是CMV领域的主流。因此,基因调控已得到更详细的阐明。然而,病毒基因调控在很大程度上受细胞和病毒成分的共同控制。换句话说,病毒基因表达由病毒-宿主相互作用决定。一般来说,细胞以防御模式对病毒感染做出反应;与此同时,病毒试图对抗细胞防御或隐藏在宿主中(潜伏)。病毒进化出有效的策略来对抗细胞防御,以实现复制成功。无论成功与否,细胞防御在整个病毒复制周期中都存在:进入、即刻早期(IE)基因表达、早期基因表达、DNA复制、晚期基因表达和病毒释放。许多针对细胞防御的病毒策略,且发生在病毒感染的即刻早期,已有文献记载。在本综述中,我们将总结已报道的IE1和pp71蛋白的生物学功能,特别是关于它们如何对抗细胞固有防御。