Construction and Generation of a Recombinant Senecavirus a Stably Expressing the NanoLuc Luciferase for Quantitative Antiviral Assay

Senecavirus A (SVA), also known as Seneca Valley virus, is a recently emerged picornavirus that can cause swine vesicular disease, posing a great threat to the global swine industry. A recombinant reporter virus (rSVA-Nluc) stably expressing the nanoluciferase (Nluc) gene between SVA 2A and 2B was d...

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Published inFrontiers in microbiology Vol. 12; p. 745502
Main Authors Guo, Xiaoran, Zhao, Kuan, Liu, Xiaona, Lei, Baishi, Zhang, Wuchao, Li, Xiuli, Yuan, Wanzhe
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 01.10.2021
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Summary:Senecavirus A (SVA), also known as Seneca Valley virus, is a recently emerged picornavirus that can cause swine vesicular disease, posing a great threat to the global swine industry. A recombinant reporter virus (rSVA-Nluc) stably expressing the nanoluciferase (Nluc) gene between SVA 2A and 2B was developed to rapidly detect anti-SVA neutralizing antibodies and establish a high-throughput screen for antiviral agents. This recombinant virus displayed similar growth kinetics as the parental virus and remained stable for more than 10 passages in BHK-21 cells. As a proof-of-concept for its utility for rapid antiviral screening, this reporter virus was used to rapidly quantify anti-SVA neutralizing antibodies in 13 swine sera samples and screen for antiviral agents, including interferons ribavirin and interferon-stimulated genes (ISGs). Subsequently, interfering RNAs targeting different regions of the SVA genome were screened using the reporter virus. This reporter virus (rSVA-Nluc) represents a useful tool for rapid and quantitative screening and evaluation of antivirals against SVA.
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Reviewed by: Qinfeng Huang, University of Minnesota Twin Cities, United States; Rui Guo, Brigham and Women’s Hospital and Harvard Medical School, United States
Edited by: Chunfu Zheng, University of Calgary, Canada
This article was submitted to Virology, a section of the journal Frontiers in Microbiology
These authors have contributed equally to this work and share first authorship
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2021.745502