Liu Chang, Liang Zhipin, Kong Xiaohong
Medical Molecular Virology Laboratory, School of Medicine, Nankai UniversityTianjin, China.
Front Microbiol. 2017 Aug 29;8:1651. doi: 10.3389/fmicb.2017.01651. eCollection 2017.
Combinatorial small interfering RNA duplexes (siRNAs) have the potential to be a gene therapy against HIV-1, and some studies have reported that transient combinatorial siRNA expression represses HIV replication, but the effects of long-term siRNA expression on HIV replication have not been studied in detail. In this study, HIV-1 replication under the influence of stable combinatorial siRNA expression from a single RNA transcript was analyzed. First, a series of cassettes encoding short hairpin RNA (shRNA)/long hairpin RNA (lhRNA)/double long hairpins (dlhRNA) was constructed and subjected to an analysis of inhibitory efficacy. Next, an optimized dlhRNA encoding cassette was selected and inserted into lentiviral delivery vector FG12. Transient dlhRNA expression reduced replication of HIV-1 in TZM-bl cells and CD4+ T cells successfully. HIV-1 susceptible TZM-bl cells were transducted with the dlhRNA expressing lentiviral vector and sorted by fluorescence-activated cell sorting to obtain stable dlhRNA expressing cells. The generation of four anti-HIV siRNAs in these dlhRNA expressing cells was verified by stem-loop RT-PCR assay. dlhRNA expression did not activate a non-specific interferon response. The dlhRNA expressing cells were also challenged with HIV-1 NL4-3, which revealed that stable expression of combinatorial siRNAs repressed HIV-1 replication for 8 days, after which HIV-1 overcame the inhibitory effect of siRNA expression by expressing mutant versions of RNAi targets. The results of this evaluation of the long-term inhibitory effects of combinatorial siRNAs against HIV-1 provide a reference for researchers who utilize combinatorial RNA interference against HIV-1 or other error-prone viruses.
组合式小干扰RNA双链体(siRNAs)有潜力成为一种抗HIV-1的基因疗法,一些研究报告称瞬时组合式siRNA表达可抑制HIV复制,但长期siRNA表达对HIV复制的影响尚未得到详细研究。在本研究中,分析了来自单个RNA转录本的稳定组合式siRNA表达影响下的HIV-1复制情况。首先,构建了一系列编码短发夹RNA(shRNA)/长发夹RNA(lhRNA)/双长发夹(dlhRNA)的盒式结构,并对其抑制效果进行分析。接下来,选择优化后的dlhRNA编码盒并插入慢病毒递送载体FG12。瞬时dlhRNA表达成功降低了HIV-1在TZM-bl细胞和CD4+ T细胞中的复制。用表达dlhRNA的慢病毒载体转导HIV-1易感TZM-bl细胞,并通过荧光激活细胞分选进行分选,以获得稳定表达dlhRNA的细胞。通过茎环RT-PCR检测验证了这些表达dlhRNA的细胞中四种抗HIV siRNA的产生。dlhRNA表达未激活非特异性干扰素反应。还用HIV-1 NL4-3攻击表达dlhRNA的细胞,结果显示组合式siRNAs的稳定表达可抑制HIV-1复制8天,之后HIV-1通过表达RNAi靶点的突变体版本克服了siRNA表达的抑制作用。对组合式siRNAs抗HIV-1长期抑制作用的评估结果为利用组合式RNA干扰对抗HIV-1或其他易出错病毒的研究人员提供了参考。