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一种新型的微小环载体系统,用于抑制肠道病毒 71 型和柯萨奇病毒 A16 的复制和基因表达。

A novel minicircle vector based system for inhibting the replication and gene expression of enterovirus 71 and coxsackievirus A16.

机构信息

CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Antiviral Res. 2012 Nov;96(2):234-44. doi: 10.1016/j.antiviral.2012.08.003. Epub 2012 Aug 17.

DOI:10.1016/j.antiviral.2012.08.003
PMID:22921338
Abstract

Enterovirus 71 (EV 71) and Coxsackievirus A16 (CA 16) are two major causative agents of hand, foot and mouth disease (HFMD). They have been associated with severe neurological and cardiological complications worldwide, and have caused significant mortalities during large-scale outbreaks in China. Currently, there are no effective treatments against EV 71 and CA 16 infections. We now describe the development of a novel minicircle vector based RNA interference (RNAi) system as a therapeutic approach to inhibiting EV 71 and CA 16 replication. Small interfering RNA (siRNA) molecules targeting the conserved regions of the 3C(pro) and 3D(pol) function gene of the EV 71 and CA 16 China strains were designed based on their nucleotide sequences available in GenBank. This RNAi system was found to effectively block the replication and gene expression of these viruses in rhabdomyosarcoma (RD) cells and virus-infected mice model. The inhibitory effects were confirmed by a corresponding decrease in viral RNA, viral protein, and progeny virus production. In addition, no significant adverse off-target silencing or cytotoxic effects were observed. These results demonstrated the potential and feasibility of this novel minicircle vector based RNAi system for antiviral therapy against EV 71 and CA 16 infection.

摘要

肠道病毒 71 型(EV 71)和柯萨奇病毒 A16 型(CA 16)是手足口病(HFMD)的两个主要病原体。它们与全球范围内严重的神经和心血管并发症有关,并在中国的大规模暴发中造成了重大死亡。目前,针对 EV 71 和 CA 16 感染还没有有效的治疗方法。我们现在描述了一种新型的微小环载体基于 RNA 干扰(RNAi)系统的开发,作为抑制 EV 71 和 CA 16 复制的治疗方法。根据 EV 71 和 CA 16 中国株在 GenBank 中可用的核苷酸序列,设计了针对 3C(pro)和 3D(pol)功能基因保守区的小干扰 RNA(siRNA)分子。该 RNAi 系统被发现能有效阻断横纹肌肉瘤(RD)细胞和病毒感染小鼠模型中这些病毒的复制和基因表达。通过相应减少病毒 RNA、病毒蛋白和子代病毒的产生,证实了抑制作用。此外,没有观察到明显的脱靶沉默或细胞毒性副作用。这些结果表明,这种新型微小环载体基于 RNAi 系统具有针对 EV 71 和 CA 16 感染的抗病毒治疗的潜力和可行性。

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