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表达针对核衣壳基因的短发夹RNA的质粒在体内抑制猪德尔塔冠状病毒的复制。

Plasmids Expressing shRNAs Specific to the Nucleocapsid Gene Inhibit the Replication of Porcine Deltacoronavirus In Vivo.

作者信息

Gu Jun, Li Hao, Bi Zhen, Li Kai, Li Zhiquan, Song Deping, Ding Zhen, He Houjun, Wu Qiong, Huang Dongyan, Gan Ping, Ye Yu, Tang Yuxin

机构信息

Department of Preventive Veterinary Medicine, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China.

Jiangxi Engineering Research Center for Animal Health Products, Nanchang 330045, China.

出版信息

Animals (Basel). 2021 Apr 23;11(5):1216. doi: 10.3390/ani11051216.

Abstract

Porcine deltacoronavirus (PDCoV) is a novel enteric coronavirus and is becoming one of the major causative agents of diarrhea in pig herds in recent years. To date, there are no commercial vaccines or antiviral pharmaceutical agents available to control PDCoV infection. Therefore, developing a reliable strategy against PDCoV is urgently needed. In this study, to observe the antiviral activity of RNA interference (RNAi), four short hairpin RNAs (shRNAs) specific to the nucleocapsid (N) gene of PDCoV were designed and tested in vitro. Of these, a double-shRNA-expression vector, designated as pSil-double-shRNA-N1, was the most effectively expressed, and the inhibition of PDCoV replication was then further evaluated in neonatal piglets. Our preliminary results reveal that plasmid-based double-shRNA-expression targeting the N gene of PDCoV can significantly protect LLC-PK1 cells and piglets from pathological lesions induced by PDCoV. Our study could benefit the investigation of the specific functions of viral genes related to PDCoV infection and offer a possible methodology of RNAi-based therapeutics for PDCoV infection.

摘要

猪德尔塔冠状病毒(PDCoV)是一种新型肠道冠状病毒,近年来正成为猪群腹泻的主要致病原之一。迄今为止,尚无用于控制PDCoV感染的商业疫苗或抗病毒药物。因此,迫切需要制定一种可靠的抗PDCoV策略。在本研究中,为了观察RNA干扰(RNAi)的抗病毒活性,设计了4条针对PDCoV核衣壳(N)基因的短发夹RNA(shRNA)并在体外进行了测试。其中,一种名为pSil-双shRNA-N1的双shRNA表达载体表达最为有效,随后在新生仔猪中进一步评估了其对PDCoV复制的抑制作用。我们的初步结果表明,靶向PDCoV N基因的基于质粒的双shRNA表达可显著保护LLC-PK1细胞和仔猪免受PDCoV诱导的病理损伤。我们的研究可能有助于对与PDCoV感染相关的病毒基因的特定功能进行研究,并为基于RNAi的PDCoV感染治疗提供一种可能的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aedc/8145914/125528f8dc50/animals-11-01216-g001.jpg

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