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牛副流感病毒3c型反向遗传系统的构建与鉴定作为快速筛选抗病毒药物的工具

Construction and characterization of a reverse genetics system of bovine parainfluenza virus type 3c as a tool for rapid screening of antivirals .

作者信息

Han Yu, Lu Kejia, Zhang Riteng, Wei Xi, Guo Hanwei, Tong Lina, Wang Xinglong, Xiao Sa, Liu Haijin, Yang Zengqi

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, China.

College of Agriculture and Animal Husbandry, Qinghai University, Xining, China.

出版信息

Front Vet Sci. 2024 Mar 12;11:1336663. doi: 10.3389/fvets.2024.1336663. eCollection 2024.

Abstract

Bovine parainfluenza virus type 3 (BPIV3) is a key pathogen associated with bovine respiratory disease complex (BRDC). However, its specific pathogenesis mechanisms have not been fully elucidated. Reverse genetics provides a useful method for understanding the pathogenic mechanism of BPIV3. To ensure the functionality of the rescue platforms, we first constructed a minigenome (MG) system of BPIV3 utilizing a 5-plasmid system in this investigation. Then, a full-length infection clone of BPIV3 was obtained from the SX-2021 strain, and different methods were employed to identify the rescued virus. Additionally, we recovered a recombinant BPIV3 using the reverse genetics system that could express enhanced green fluorescence protein (eGFP). Through the growth curve assays, the replicate capability of rBPIV3-SX-EGFP was found to be similar to that of the parental virus. Subsequently, the rBPIV3-SX-EGFP was used to determine the antiviral activity of ribavirin. The results showed that ribavirin had an anti-BPIV3 effect in MDBK cells. In conclusion, the successful development of a reverse genetic system for the SX-2021 strain establishes a foundation for future studies on BPIV3, including investigations into its pathogenic mechanism, gene function, and antiviral screening properties.

摘要

牛副流感病毒3型(BPIV3)是与牛呼吸道疾病综合征(BRDC)相关的关键病原体。然而,其具体发病机制尚未完全阐明。反向遗传学为理解BPIV3的致病机制提供了一种有用的方法。为确保拯救平台的功能,在本研究中,我们首先利用五质粒系统构建了BPIV3的微型基因组(MG)系统。然后,从SX-2021毒株获得了BPIV3的全长感染性克隆,并采用不同方法鉴定拯救出的病毒。此外,我们利用反向遗传学系统拯救出了一种能表达增强型绿色荧光蛋白(eGFP)的重组BPIV3。通过生长曲线测定,发现rBPIV3-SX-EGFP的复制能力与亲本病毒相似。随后,用rBPIV3-SX-EGFP测定利巴韦林的抗病毒活性。结果表明,利巴韦林在MDBK细胞中具有抗BPIV3作用。总之,成功开发出SX-2021毒株的反向遗传系统为未来BPIV3的研究奠定了基础,包括对其致病机制、基因功能和抗病毒筛选特性的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4522/10967227/1ef6b1679435/fvets-11-1336663-g001.jpg

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