Department of Microbiology & Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834, United States; Faculty of Science, Al Azhar University, Assiut Branch, Assiut 71524, Egypt.
Department of Medicine (Division of Hematology/Oncology), Brody School of Medicine, East Carolina University, Greenville, NC 27834, United States; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh 11433, Saudi Arabia.
Virus Res. 2019 Jun;266:15-24. doi: 10.1016/j.virusres.2019.03.024. Epub 2019 Apr 2.
Kaposi's sarcoma-associated herpesvirus (KSHV) is the etiological agent of Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castleman Disease (MCD). Recent mechanistic advances have discerned the importance of microRNAs in the virus-host relationship. KSHV has two modes of replication: lytic and latent phase. KSHV entry into permissive cells, establishment of infection, and maintenance of latency are contingent upon successful modulation of the host miRNA transcriptome. Apart from host cell miRNAs, KSHV also encodes viral miRNAs. Among various cellular and molecular targets, miRNAs are appearing to be key players in regulating viral pathogenesis. Therefore, the use of miRNAs as novel therapeutics has gained considerable attention as of late. This innovative approach relies on either mimicking miRNA species by identical oligonucleotides, or selective silencing of miRNA with specific oligonucleotide inhibitors. Here, we provide an overview of KSHV pathogenesis at the molecular level with special emphasis on the various roles miRNAs play during virus infection.
卡波济肉瘤相关疱疹病毒(KSHV)是卡波济肉瘤(KS)、原发性渗出性淋巴瘤(PEL)和多中心卡斯特曼病(MCD)的病因。最近的机制研究进展表明,microRNAs 在病毒-宿主关系中具有重要作用。KSHV 有两种复制方式:裂解和潜伏阶段。KSHV 进入允许的细胞、建立感染和维持潜伏状态,取决于宿主 miRNA 转录组的成功调节。除了宿主细胞 miRNA 外,KSHV 还编码病毒 miRNA。在各种细胞和分子靶标中,miRNA 似乎是调节病毒发病机制的关键因素。因此,miRNA 作为新型治疗方法最近引起了相当大的关注。这种创新方法依赖于用相同的寡核苷酸模拟 miRNA 种类,或用特异性寡核苷酸抑制剂选择性沉默 miRNA。在这里,我们提供了 KSHV 发病机制在分子水平上的概述,特别强调了 miRNA 在病毒感染过程中所扮演的各种角色。