Centre for Inflammation Research, Institute of Regeneration and Repair, The University of Edinburgh, Edinburgh, United Kingdom.
Division of Infectious Diseases & Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
mBio. 2023 Dec 19;14(6):e0257221. doi: 10.1128/mbio.02572-21. Epub 2023 Oct 26.
Intracellular innate immunity involves co-evolved antiviral restriction factors that specifically inhibit infecting viruses. Studying these restrictions has increased our understanding of viral replication, host-pathogen interactions, and pathogenesis, and represent potential targets for novel antiviral therapies. Lentiviral restriction 2 (Lv2) was identified as an unmapped early-phase restriction of HIV-2 and later shown to also restrict HIV-1 and simian immunodeficiency virus. The viral determinants of Lv2 susceptibility have been mapped to the envelope and capsid proteins in both HIV-1 and HIV-2, and also viral protein R (Vpr) in HIV-1, and appears dependent on cellular entry mechanism. A genome-wide screen identified several likely contributing host factors including members of the polymerase-associated factor 1 (PAF1) and human silencing hub (HUSH) complexes, and the newly characterized regulation of nuclear pre-mRNA domain containing 2 (RPRD2). Subsequently, RPRD2 (or RNA-associated early-stage antiviral factor) has been shown to be upregulated upon T cell activation, is highly expressed in myeloid cells, binds viral reverse transcripts, and potently restricts HIV-1 infection. RPRD2 is also bound by HIV-1 Vpr and targeted for degradation by the proteasome upon reverse transcription, suggesting RPRD2 impedes reverse transcription and Vpr targeting overcomes this block. RPRD2 is mainly localized to the nucleus and binds RNA, DNA, and DNA:RNA hybrids. More recently, RPRD2 has been shown to negatively regulate genome-wide transcription and interact with the HUSH and PAF1 complexes which repress HIV transcription and are implicated in maintenance of HIV latency. In this review, we examine Lv2 restriction and the antiviral role of RPRD2 and consider potential mechanism(s) of action.
细胞内固有免疫涉及共同进化的抗病毒限制因子,这些因子专门抑制感染病毒。研究这些限制因素增加了我们对病毒复制、宿主-病原体相互作用和发病机制的理解,并且代表了新型抗病毒治疗的潜在靶点。慢病毒限制因子 2 (Lv2) 被确定为 HIV-2 的早期阶段限制因子,后来也被证明可以限制 HIV-1 和猴免疫缺陷病毒。Lv2 易感性的病毒决定因素已映射到 HIV-1 和 HIV-2 的包膜和衣壳蛋白,以及 HIV-1 的病毒蛋白 R (Vpr),并且似乎依赖于细胞进入机制。全基因组筛选鉴定了几种可能的宿主因子,包括聚合酶相关因子 1 (PAF1) 和人类沉默中心 (HUSH) 复合物的成员,以及新鉴定的调节核前体 RNA 结构域包含蛋白 2 (RPRD2)。随后,RPRD2(或 RNA 相关早期抗病毒因子)在 T 细胞激活时被上调,在髓样细胞中高度表达,结合病毒逆转录物,并强烈限制 HIV-1 感染。RPRD2 也被 HIV-1 Vpr 结合,并在逆转录时被蛋白酶体靶向降解,表明 RPRD2 阻碍逆转录,而 Vpr 靶向克服了这种阻碍。RPRD2 主要定位于细胞核,结合 RNA、DNA 和 DNA:RNA 杂交体。最近,RPRD2 被证明可以负调控全基因组转录,并与 HUSH 和 PAF1 复合物相互作用,这些复合物抑制 HIV 转录,并与 HIV 潜伏的维持有关。在这篇综述中,我们研究了 Lv2 限制和 RPRD2 的抗病毒作用,并考虑了潜在的作用机制。