College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu Province, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonosis, Yangzhou, 225009, Jiangsu Province, China.
Virol J. 2023 Jul 24;20(1):164. doi: 10.1186/s12985-023-02129-5.
Porcine epidemic diarrhea virus (PEDV) is an α-coronavirus that causes highly contagious intestinal infectious disease, involving clinically characterized by diarrhea, dehydration, vomiting, and high mortality to suckling piglets. As a strategy for antiviral therapy, artificial microRNA (amiRNA) mediated suppression of viral replication has recently become increasingly important. In this study, we evaluated the advantages of using an amiRNA vector against PEDV.
In this study, we evaluated the advantages of using an amiRNA vector against PEDV. We designed two single amiRNA sequences for different conserved sequences of the PEDV S and N genes, and tested their inhibitory effects on PEDV in Vero cells.
It was obvious from the CCK-8 results that the transient transfection of amiRNA was non-toxic to the cells. In addition, our results showed that the transient expression of two amiRNAs (amiRNA-349 and amiRNA-1447) significantly reduced the expression of viral RNA and protein in the cells. The TCID results showed that the release of virus particles into the culture supernatant was significantly reduced, with an effect as high as 90%. To avoid virus mutation escape, the above two single amiRNA sequences were tandem in this study (amiRNA-349 + 1447), enabling a single microRNA to be expressed simultaneously. The real-time PCR and Western blot results showed that the inhibitory effect was significantly enhanced in each of the different time periods. The TCID results showed that the release of virus particles in the culture supernatant was significantly reduced at the different time periods.
In summary, these results suggest that an RNAi based on amiRNA targeting the conserved region of the virus is an effective method to improve PEDV nucleic acid inhibitors and provide a novel treatment strategy for PEDV infection.
猪流行性腹泻病毒(PEDV)是一种α冠状病毒,可引起高度传染性的肠道传染病,临床上以仔猪腹泻、脱水、呕吐和高死亡率为特征。作为抗病毒治疗策略,人工 microRNA(amiRNA)介导的病毒复制抑制最近变得越来越重要。在本研究中,我们评估了针对 PEDV 使用 amiRNA 载体的优势。
在本研究中,我们评估了针对 PEDV 使用 amiRNA 载体的优势。我们设计了针对 PEDV S 和 N 基因不同保守序列的两个单 amiRNA 序列,并在 Vero 细胞中测试了它们对 PEDV 的抑制作用。
从 CCK-8 结果明显看出,amiRNA 的瞬时转染对细胞无毒。此外,我们的结果表明,两种 amiRNA(amiRNA-349 和 amiRNA-1447)的瞬时表达显著降低了细胞中病毒 RNA 和蛋白的表达。TCID 结果表明,病毒粒子释放到培养上清液中的明显减少,效果高达 90%。为了避免病毒突变逃逸,本研究中将上述两个单 amiRNA 序列串联(amiRNA-349+1447),使单个 microRNA 能够同时表达。实时 PCR 和 Western blot 结果表明,在每个不同的时间段,抑制效果都明显增强。TCID 结果表明,在不同的时间段,培养上清液中病毒粒子的释放明显减少。
总之,这些结果表明,基于针对病毒保守区域的 amiRNA 的 RNAi 是提高 PEDV 核酸抑制剂的有效方法,并为 PEDV 感染提供了一种新的治疗策略。