Poeschla Eric M
Department of Molecular Medicine and Division of Infectious Diseases, Guggenheim 18, College of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Vet Immunol Immunopathol. 2011 Oct 15;143(3-4):215-20. doi: 10.1016/j.vetimm.2011.06.014. Epub 2011 Jun 12.
Retroviral restriction factor research is explaining long-standing lentiviral mysteries. Asking why a particular retrovirus cannot complete a critical part of its life cycle in cells of a particular species has been the starting point for numerous discoveries, including heretofore elusive functions of HIV-1 accessory genes. The potential for therapeutic application is substantial. Analyzing the feline immunodeficiency virus (FIV) life cycle has been instrumental and the source of some surprising observations in this field. FIV is restricted in cells of various primates by several restriction factors including APOBEC3 proteins and, uniquely, TRIM proteins from both Old and New World monkeys. In contrast, the feline genome does not encode functional TRIM5alpha or TRIMCyp proteins and HIV-1 is primarily blocked in feline cells by APOBEC3 proteins. These can be overcome by inserting FIV vif or even SIVmac vif into HIV-1. The domestic cat and its lentivirus are positioned to offer strategic research opportunities as the field moves forward.
逆转录病毒限制因子的研究正在解开长期存在的慢病毒谜团。探究为何特定逆转录病毒无法在特定物种的细胞中完成其生命周期的关键部分,一直是众多发现的起点,包括迄今难以捉摸的HIV-1辅助基因的功能。其治疗应用潜力巨大。分析猫免疫缺陷病毒(FIV)的生命周期在该领域发挥了重要作用,并带来了一些惊人的发现。FIV在各种灵长类动物的细胞中受到多种限制因子的限制,包括载脂蛋白B mRNA编辑酶催化多肽样3(APOBEC3)蛋白,以及旧世界和新世界猴子独特的TRIM蛋白。相比之下,猫基因组不编码功能性TRIM5α或TRIMCyp蛋白,HIV-1在猫细胞中主要被APOBEC3蛋白阻断。通过将FIV病毒感染因子(vif)甚至猴免疫缺陷病毒(SIVmac)的vif插入HIV-1中,可以克服这些限制。随着该领域的发展,家猫及其慢病毒有望提供战略研究机会。