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Development of A MERS-CoV Replicon Cell Line for Antiviral Screening

Middle East respiratory syndrome coronavirus (MERS-CoV) is the causative agent of a severe respiratory disease with a high mortality of ~ 35%. The lack of approved treatments for MERS-CoV infection underscores the need for a user-friendly system for rapid drug screening. In this study, we constructe...

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Autores principales: Chen, Jing, Hu, Bing-Jie, Zhao, Kai, Luo, Yun, Lin, Hao-Feng, Shi, Zheng-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898024/
https://www.ncbi.nlm.nih.gov/pubmed/33616893
http://dx.doi.org/10.1007/s12250-020-00341-z
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author Chen, Jing
Hu, Bing-Jie
Zhao, Kai
Luo, Yun
Lin, Hao-Feng
Shi, Zheng-Li
author_facet Chen, Jing
Hu, Bing-Jie
Zhao, Kai
Luo, Yun
Lin, Hao-Feng
Shi, Zheng-Li
author_sort Chen, Jing
collection PubMed
description Middle East respiratory syndrome coronavirus (MERS-CoV) is the causative agent of a severe respiratory disease with a high mortality of ~ 35%. The lack of approved treatments for MERS-CoV infection underscores the need for a user-friendly system for rapid drug screening. In this study, we constructed a MERS-CoV replicon containing the Renilla luciferase (Rluc) reporter gene and a stable luciferase replicon-carrying cell line. Using this cell line, we showed that MERS-CoV replication was inhibited by combined application of lopinavir and ritonavir, indicating that this cell line can be used to screen inhibitors of MERS-CoV replication. Importantly, the MERS-replicon cell line can be used for high-throughput screening of antiviral drugs without the need for live virus handling, providing an effective and safe tool for the discovery of antiviral drugs against MERS-CoV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12250-020-00341-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-78980242021-02-22 Development of A MERS-CoV Replicon Cell Line for Antiviral Screening Chen, Jing Hu, Bing-Jie Zhao, Kai Luo, Yun Lin, Hao-Feng Shi, Zheng-Li Virol Sin Research Article Middle East respiratory syndrome coronavirus (MERS-CoV) is the causative agent of a severe respiratory disease with a high mortality of ~ 35%. The lack of approved treatments for MERS-CoV infection underscores the need for a user-friendly system for rapid drug screening. In this study, we constructed a MERS-CoV replicon containing the Renilla luciferase (Rluc) reporter gene and a stable luciferase replicon-carrying cell line. Using this cell line, we showed that MERS-CoV replication was inhibited by combined application of lopinavir and ritonavir, indicating that this cell line can be used to screen inhibitors of MERS-CoV replication. Importantly, the MERS-replicon cell line can be used for high-throughput screening of antiviral drugs without the need for live virus handling, providing an effective and safe tool for the discovery of antiviral drugs against MERS-CoV. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12250-020-00341-z) contains supplementary material, which is available to authorized users. Springer Singapore 2021-02-22 /pmc/articles/PMC7898024/ /pubmed/33616893 http://dx.doi.org/10.1007/s12250-020-00341-z Text en © Wuhan Institute of Virology, CAS 2021
spellingShingle Research Article
Chen, Jing
Hu, Bing-Jie
Zhao, Kai
Luo, Yun
Lin, Hao-Feng
Shi, Zheng-Li
Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title_full Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title_fullStr Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title_full_unstemmed Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title_short Development of A MERS-CoV Replicon Cell Line for Antiviral Screening
title_sort development of a mers-cov replicon cell line for antiviral screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898024/
https://www.ncbi.nlm.nih.gov/pubmed/33616893
http://dx.doi.org/10.1007/s12250-020-00341-z
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