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Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds

Sosuga virus (SOSV) is a recently discovered zoonotic paramyxovirus isolated from a single human case in 2012; it has been ecologically and epidemiologically associated with transmission by the Egyptian rousette bat (Rousettus aegyptiacus). Bats have long been recognized as sources of novel zoonotic...

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Autores principales: Welch, Stephen R., Chakrabarti, Ayan K., Wiggleton Guerrero, Lisa, Jenks, Harley M., Lo, Michael K., Nichol, Stuart T., Spiropoulou, Christina F., Albariño, César G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862516/
https://www.ncbi.nlm.nih.gov/pubmed/29522528
http://dx.doi.org/10.1371/journal.pntd.0006326
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author Welch, Stephen R.
Chakrabarti, Ayan K.
Wiggleton Guerrero, Lisa
Jenks, Harley M.
Lo, Michael K.
Nichol, Stuart T.
Spiropoulou, Christina F.
Albariño, César G.
author_facet Welch, Stephen R.
Chakrabarti, Ayan K.
Wiggleton Guerrero, Lisa
Jenks, Harley M.
Lo, Michael K.
Nichol, Stuart T.
Spiropoulou, Christina F.
Albariño, César G.
author_sort Welch, Stephen R.
collection PubMed
description Sosuga virus (SOSV) is a recently discovered zoonotic paramyxovirus isolated from a single human case in 2012; it has been ecologically and epidemiologically associated with transmission by the Egyptian rousette bat (Rousettus aegyptiacus). Bats have long been recognized as sources of novel zoonotic pathogens, including highly lethal paramyxoviruses like Nipah virus (NiV) and Hendra virus (HeV). The ability of SOSV to cause severe human disease supports the need for studies on SOSV pathogenesis to better understand the potential impact of this virus and to identify effective treatments. Here we describe a reverse genetics system for SOSV comprising a minigenome-based assay and a replication-competent infectious recombinant reporter SOSV that expresses the fluorescent protein ZsGreen1 in infected cells. First, we used the minigenome assay to rapidly screen for compounds inhibiting SOSV replication at biosafety level 2 (BSL-2). The antiviral activity of candidate compounds was then tested against authentic viral replication using the reporter SOSV at BSL-3. We identified several compounds with anti-SOSV activity, several of which also inhibit NiV and HeV. Alongside its utility in screening for potential SOSV therapeutics, the reverse genetics system described here is a powerful tool for analyzing mechanisms of SOSV pathogenesis, which will facilitate our understanding of how to combat the potential public health threats posed by emerging bat-borne paramyxoviruses.
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spelling pubmed-58625162018-03-28 Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds Welch, Stephen R. Chakrabarti, Ayan K. Wiggleton Guerrero, Lisa Jenks, Harley M. Lo, Michael K. Nichol, Stuart T. Spiropoulou, Christina F. Albariño, César G. PLoS Negl Trop Dis Research Article Sosuga virus (SOSV) is a recently discovered zoonotic paramyxovirus isolated from a single human case in 2012; it has been ecologically and epidemiologically associated with transmission by the Egyptian rousette bat (Rousettus aegyptiacus). Bats have long been recognized as sources of novel zoonotic pathogens, including highly lethal paramyxoviruses like Nipah virus (NiV) and Hendra virus (HeV). The ability of SOSV to cause severe human disease supports the need for studies on SOSV pathogenesis to better understand the potential impact of this virus and to identify effective treatments. Here we describe a reverse genetics system for SOSV comprising a minigenome-based assay and a replication-competent infectious recombinant reporter SOSV that expresses the fluorescent protein ZsGreen1 in infected cells. First, we used the minigenome assay to rapidly screen for compounds inhibiting SOSV replication at biosafety level 2 (BSL-2). The antiviral activity of candidate compounds was then tested against authentic viral replication using the reporter SOSV at BSL-3. We identified several compounds with anti-SOSV activity, several of which also inhibit NiV and HeV. Alongside its utility in screening for potential SOSV therapeutics, the reverse genetics system described here is a powerful tool for analyzing mechanisms of SOSV pathogenesis, which will facilitate our understanding of how to combat the potential public health threats posed by emerging bat-borne paramyxoviruses. Public Library of Science 2018-03-09 /pmc/articles/PMC5862516/ /pubmed/29522528 http://dx.doi.org/10.1371/journal.pntd.0006326 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Welch, Stephen R.
Chakrabarti, Ayan K.
Wiggleton Guerrero, Lisa
Jenks, Harley M.
Lo, Michael K.
Nichol, Stuart T.
Spiropoulou, Christina F.
Albariño, César G.
Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title_full Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title_fullStr Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title_full_unstemmed Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title_short Development of a reverse genetics system for Sosuga virus allows rapid screening of antiviral compounds
title_sort development of a reverse genetics system for sosuga virus allows rapid screening of antiviral compounds
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862516/
https://www.ncbi.nlm.nih.gov/pubmed/29522528
http://dx.doi.org/10.1371/journal.pntd.0006326
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