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Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity
Canine distemper virus (CDV), a close relative of the human pathogen measles virus (MeV), is an enveloped, negative sense RNA virus that belongs to the genus Morbillivirus and causes severe diseases in dogs and other carnivores. Although the vaccination is available as a preventive measure against t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831055/ https://www.ncbi.nlm.nih.gov/pubmed/33477492 http://dx.doi.org/10.3390/v13010128 |
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author | Shrestha, Neeta Gall, Flavio M. Vesin, Jonathan Chambon, Marc Turcatti, Gerardo Fotiadis, Dimitrios Riedl, Rainer Plattet, Philippe |
author_facet | Shrestha, Neeta Gall, Flavio M. Vesin, Jonathan Chambon, Marc Turcatti, Gerardo Fotiadis, Dimitrios Riedl, Rainer Plattet, Philippe |
author_sort | Shrestha, Neeta |
collection | PubMed |
description | Canine distemper virus (CDV), a close relative of the human pathogen measles virus (MeV), is an enveloped, negative sense RNA virus that belongs to the genus Morbillivirus and causes severe diseases in dogs and other carnivores. Although the vaccination is available as a preventive measure against the disease, the occasional vaccination failure highlights the importance of therapeutic alternatives such as antivirals against CDV. The morbilliviral cell entry system relies on two interacting envelope glycoproteins: the attachment (H) and fusion (F) proteins. Here, to potentially discover novel entry inhibitors targeting CDV H, F and/or the cognate receptor: signaling lymphocyte activation molecule (SLAM) proteins, we designed a quantitative cell-based fusion assay that matched high-throughput screening (HTS) settings. By screening two libraries of small molecule compounds, we successfully identified two membrane fusion inhibitors (F2736-3056 and F2261-0043). Although both inhibitors exhibited similarities in structure and potency with the small molecule compound 3G (an AS-48 class morbilliviral F-protein inhibitor), F2736-3056 displayed improved efficacy in blocking fusion activity when a 3G-escape variant was employed. Altogether, we present a cell-based fusion assay that can be utilized not only to discover antiviral agents against CDV but also to dissect the mechanism of morbilliviral-mediated cell-binding and cell-to-cell fusion activity. |
format | Online Article Text |
id | pubmed-7831055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78310552021-01-26 Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity Shrestha, Neeta Gall, Flavio M. Vesin, Jonathan Chambon, Marc Turcatti, Gerardo Fotiadis, Dimitrios Riedl, Rainer Plattet, Philippe Viruses Article Canine distemper virus (CDV), a close relative of the human pathogen measles virus (MeV), is an enveloped, negative sense RNA virus that belongs to the genus Morbillivirus and causes severe diseases in dogs and other carnivores. Although the vaccination is available as a preventive measure against the disease, the occasional vaccination failure highlights the importance of therapeutic alternatives such as antivirals against CDV. The morbilliviral cell entry system relies on two interacting envelope glycoproteins: the attachment (H) and fusion (F) proteins. Here, to potentially discover novel entry inhibitors targeting CDV H, F and/or the cognate receptor: signaling lymphocyte activation molecule (SLAM) proteins, we designed a quantitative cell-based fusion assay that matched high-throughput screening (HTS) settings. By screening two libraries of small molecule compounds, we successfully identified two membrane fusion inhibitors (F2736-3056 and F2261-0043). Although both inhibitors exhibited similarities in structure and potency with the small molecule compound 3G (an AS-48 class morbilliviral F-protein inhibitor), F2736-3056 displayed improved efficacy in blocking fusion activity when a 3G-escape variant was employed. Altogether, we present a cell-based fusion assay that can be utilized not only to discover antiviral agents against CDV but also to dissect the mechanism of morbilliviral-mediated cell-binding and cell-to-cell fusion activity. MDPI 2021-01-18 /pmc/articles/PMC7831055/ /pubmed/33477492 http://dx.doi.org/10.3390/v13010128 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shrestha, Neeta Gall, Flavio M. Vesin, Jonathan Chambon, Marc Turcatti, Gerardo Fotiadis, Dimitrios Riedl, Rainer Plattet, Philippe Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title | Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title_full | Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title_fullStr | Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title_full_unstemmed | Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title_short | Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity |
title_sort | antiviral screen against canine distemper virus-induced membrane fusion activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831055/ https://www.ncbi.nlm.nih.gov/pubmed/33477492 http://dx.doi.org/10.3390/v13010128 |
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