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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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. |
format | Online Article Text |
id | pubmed-7649875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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