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Generation of a reporter yellow fever virus for high throughput antiviral assays

Yellow fever virus (YFV), a member of the Flaviviridae family, is an arthropod-borne virus that can cause severe disease in humans with a lethality rate of up to 60%. Since 2017, increases in YFV activity in areas of South America and Africa have been described. Although a vaccine is available, name...

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Autores principales: Sanchez-Velazquez, Ricardo, de Lorenzo, Giuditta, Tandavanitj, Rapeepat, Setthapramote, Chayanee, Bredenbeek, Peter J., Bozzacco, Leonia, MacDonald, Margaret R., Clark, Jordan J., Rice, Charles M., Patel, Arvind H., Kohl, Alain, Varjak, Margus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649875/
https://www.ncbi.nlm.nih.gov/pubmed/32980446
http://dx.doi.org/10.1016/j.antiviral.2020.104939
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author Sanchez-Velazquez, Ricardo
de Lorenzo, Giuditta
Tandavanitj, Rapeepat
Setthapramote, Chayanee
Bredenbeek, Peter J.
Bozzacco, Leonia
MacDonald, Margaret R.
Clark, Jordan J.
Rice, Charles M.
Patel, Arvind H.
Kohl, Alain
Varjak, Margus
author_facet Sanchez-Velazquez, Ricardo
de Lorenzo, Giuditta
Tandavanitj, Rapeepat
Setthapramote, Chayanee
Bredenbeek, Peter J.
Bozzacco, Leonia
MacDonald, Margaret R.
Clark, Jordan J.
Rice, Charles M.
Patel, Arvind H.
Kohl, Alain
Varjak, Margus
author_sort Sanchez-Velazquez, Ricardo
collection PubMed
description Yellow fever virus (YFV), a member of the Flaviviridae family, is an arthropod-borne virus that can cause severe disease in humans with a lethality rate of up to 60%. Since 2017, increases in YFV activity in areas of South America and Africa have been described. Although a vaccine is available, named strain 17D (Theiler and Smith, 1937), it is contraindicated for use in the elderly, expectant mothers, immunocompromised people, among others. To this day there is no antiviral treatment against YFV to reduce the severity of viral infection. Here, we used a circular polymerase extension reaction (CPER)-based reverse genetics approach to generate a full-length reporter virus (YFVhb) by introducing a small HiBit tag in the NS1 protein. The reporter virus replicates at a similar rate to the parental YFV in HuH-7 cells. Using YFVhb, we designed a high throughput antiviral screening luciferase-based assay to identify inhibitors that target any step of the viral replication cycle. We validated our assay by using a range of inhibitors including drugs, immune sera and neutralizing single chain variable fragments (scFv). In light of the recent upsurge in YFV and a potential spread of the virus, this assay is a further tool in the development of antiviral therapy against YFV.
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spelling pubmed-76498752020-11-16 Generation of a reporter yellow fever virus for high throughput antiviral assays Sanchez-Velazquez, Ricardo de Lorenzo, Giuditta Tandavanitj, Rapeepat Setthapramote, Chayanee Bredenbeek, Peter J. Bozzacco, Leonia MacDonald, Margaret R. Clark, Jordan J. Rice, Charles M. Patel, Arvind H. Kohl, Alain Varjak, Margus Antiviral Res Research Paper Yellow fever virus (YFV), a member of the Flaviviridae family, is an arthropod-borne virus that can cause severe disease in humans with a lethality rate of up to 60%. Since 2017, increases in YFV activity in areas of South America and Africa have been described. Although a vaccine is available, named strain 17D (Theiler and Smith, 1937), it is contraindicated for use in the elderly, expectant mothers, immunocompromised people, among others. To this day there is no antiviral treatment against YFV to reduce the severity of viral infection. Here, we used a circular polymerase extension reaction (CPER)-based reverse genetics approach to generate a full-length reporter virus (YFVhb) by introducing a small HiBit tag in the NS1 protein. The reporter virus replicates at a similar rate to the parental YFV in HuH-7 cells. Using YFVhb, we designed a high throughput antiviral screening luciferase-based assay to identify inhibitors that target any step of the viral replication cycle. We validated our assay by using a range of inhibitors including drugs, immune sera and neutralizing single chain variable fragments (scFv). In light of the recent upsurge in YFV and a potential spread of the virus, this assay is a further tool in the development of antiviral therapy against YFV. Elsevier 2020-11 /pmc/articles/PMC7649875/ /pubmed/32980446 http://dx.doi.org/10.1016/j.antiviral.2020.104939 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Sanchez-Velazquez, Ricardo
de Lorenzo, Giuditta
Tandavanitj, Rapeepat
Setthapramote, Chayanee
Bredenbeek, Peter J.
Bozzacco, Leonia
MacDonald, Margaret R.
Clark, Jordan J.
Rice, Charles M.
Patel, Arvind H.
Kohl, Alain
Varjak, Margus
Generation of a reporter yellow fever virus for high throughput antiviral assays
title Generation of a reporter yellow fever virus for high throughput antiviral assays
title_full Generation of a reporter yellow fever virus for high throughput antiviral assays
title_fullStr Generation of a reporter yellow fever virus for high throughput antiviral assays
title_full_unstemmed Generation of a reporter yellow fever virus for high throughput antiviral assays
title_short Generation of a reporter yellow fever virus for high throughput antiviral assays
title_sort generation of a reporter yellow fever virus for high throughput antiviral assays
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649875/
https://www.ncbi.nlm.nih.gov/pubmed/32980446
http://dx.doi.org/10.1016/j.antiviral.2020.104939
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