Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, E1 2AT, United Kingdom.
Division of Infection and Pathway Medicine, School of Biomedical Sciences, University of Edinburgh, Edinburgh, EH16 4SB, United Kingdom.
Sci Rep. 2018 Sep 28;8(1):14551. doi: 10.1038/s41598-018-32785-5.
Interferon induced transmembrane proteins (IFITMs) inhibit the cellular entry of a broad range of viruses, but it has been suspected that for HIV-1 IFITMs may also inhibit a post-integration replicative step. We show that IFITM expression reduces HIV-1 viral protein synthesis by preferentially excluding viral mRNA transcripts from translation and thereby restricts viral production. Codon-optimization of proviral DNA rescues viral translation, implying that IFITM-mediated restriction requires recognition of viral RNA elements. In addition, we find that expression of the viral accessory protein Nef can help overcome the IFITM-mediated inhibition of virus production. Our studies identify a novel role for IFITMs in inhibiting HIV replication at the level of translation, but show that the effects can be overcome by the lentiviral protein Nef.
干扰素诱导跨膜蛋白(IFITMs)抑制广泛的病毒进入细胞,但人们怀疑对于 HIV-1,IFITMs 也可能抑制整合后的复制步骤。我们表明,IFITM 的表达通过优先将病毒 mRNA 转录本排除在翻译之外,从而降低 HIV-1 病毒蛋白的合成,从而限制了病毒的产生。前病毒 DNA 的密码子优化挽救了病毒的翻译,这表明 IFITM 介导的限制需要识别病毒 RNA 元件。此外,我们发现表达病毒辅助蛋白 Nef 可以帮助克服 IFITM 对病毒产生的抑制作用。我们的研究在翻译水平上确定了 IFITMs 抑制 HIV 复制的新作用,但表明这种作用可以被慢病毒蛋白 Nef 克服。