Israsena Nipan, Supavonwong Pornpan, Ratanasetyuth Nitipol, Khawplod Pakamatz, Hemachudha Thiravat
Department of Pharmacology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Antiviral Res. 2009 Oct;84(1):76-83. doi: 10.1016/j.antiviral.2009.07.012. Epub 2009 Jul 29.
The RNA interference (RNAi) technology has been recognized as a promising antiviral therapy for a few years. One of the potential limitations for applying this technology against wild type rabies virus is its high rate of genetic variation. Recently, an RNAi vector system that incorporated modified dsRNA within microRNA structure [or artificial miRNAs(amiRNAs)] has been described. This allowed expression of multiple amiRNAs of single or multiple targets from a single construct. In this study, we evaluated a benefit of using amiRNA vector against different rabies strains. We found that applying single targeting amiRNA against challenged rabies virus standard (CVS) rabies nucleocapsid (N) mRNA resulted in more than 90% reduction of viral genome in Neuro2A cells up to 72 h after infection. Multiple amiRNAs aiming at single or multiple NmRNA target(s) yielded comparable inhibitory results as with a single amiRNA against perfectly matched target. Although the level of each mature miRNA generated from multiple amiRNA construct was slightly reduced as assessed by stem-loop RT and real-time PCR techniques, its effectiveness remained unchanged even when an ineffective or scrambled amiRNA was also included in the transcript. Against highly pathogenic wild type virus, single amiRNA construct activity was reduced when mismatching with target sequence occurred at critical site whereas multiple targeting amiRNA construct remained highly effective. Our results suggest the benefit of using multiple targeting amiRNAs when confronting with wild type rabies virus, the sequence of which is not completely known.
RNA干扰(RNAi)技术在过去几年中已被公认为一种有前景的抗病毒疗法。将该技术应用于野生型狂犬病病毒的一个潜在限制是其高遗传变异率。最近,一种在微小RNA结构中整合了修饰双链RNA的RNAi载体系统(即人工微小RNA,amiRNA)已被报道。这使得从单个构建体中表达针对单个或多个靶标的多个amiRNA成为可能。在本研究中,我们评估了使用amiRNA载体对抗不同狂犬病病毒株的益处。我们发现,针对攻击的狂犬病病毒标准株(CVS)的核衣壳(N)mRNA应用单靶点amiRNA,在感染后长达72小时内,Neuro2A细胞中的病毒基因组减少了90%以上。针对单个或多个N mRNA靶点的多个amiRNA产生了与针对完全匹配靶点的单个amiRNA相当的抑制效果。尽管通过茎环RT和实时PCR技术评估,从多个amiRNA构建体产生的每个成熟miRNA的水平略有降低,但即使转录本中还包含无效或乱序的amiRNA,其有效性仍保持不变。对于高致病性野生型病毒,当关键位点与靶序列发生错配时,单amiRNA构建体的活性降低,而多靶点amiRNA构建体仍保持高效。我们的结果表明,在面对序列不完全清楚的野生型狂犬病病毒时,使用多靶点amiRNA是有益的。