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A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures
Filoviruses, such as Ebola virus and Marburg virus, are of significant human health concern. From 2013 to 2016, Ebola virus caused 11,323 fatalities in Western Africa. Since 2018, two Ebola virus disease outbreaks in the Democratic Republic of the Congo resulted in 2354 fatalities. Although there is...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824103/ https://www.ncbi.nlm.nih.gov/pubmed/33396288 http://dx.doi.org/10.3390/v13010052 |
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author | Bennett, Ryan P. Finch, Courtney L. Postnikova, Elena N. Stewart, Ryan A. Cai, Yingyun Yu, Shuiqing Liang, Janie Dyall, Julie Salter, Jason D. Smith, Harold C. Kuhn, Jens H. |
author_facet | Bennett, Ryan P. Finch, Courtney L. Postnikova, Elena N. Stewart, Ryan A. Cai, Yingyun Yu, Shuiqing Liang, Janie Dyall, Julie Salter, Jason D. Smith, Harold C. Kuhn, Jens H. |
author_sort | Bennett, Ryan P. |
collection | PubMed |
description | Filoviruses, such as Ebola virus and Marburg virus, are of significant human health concern. From 2013 to 2016, Ebola virus caused 11,323 fatalities in Western Africa. Since 2018, two Ebola virus disease outbreaks in the Democratic Republic of the Congo resulted in 2354 fatalities. Although there is progress in medical countermeasure (MCM) development (in particular, vaccines and antibody-based therapeutics), the need for efficacious small-molecule therapeutics remains unmet. Here we describe a novel high-throughput screening assay to identify inhibitors of Ebola virus VP40 matrix protein association with viral particle assembly sites on the interior of the host cell plasma membrane. Using this assay, we screened nearly 3000 small molecules and identified several molecules with the desired inhibitory properties. In secondary assays, one identified compound, sangivamycin, inhibited not only Ebola viral infectivity but also that of other viruses. This finding indicates that it is possible for this new VP40-based screening method to identify highly potent MCMs against Ebola virus and its relatives. |
format | Online Article Text |
id | pubmed-7824103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78241032021-01-24 A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures Bennett, Ryan P. Finch, Courtney L. Postnikova, Elena N. Stewart, Ryan A. Cai, Yingyun Yu, Shuiqing Liang, Janie Dyall, Julie Salter, Jason D. Smith, Harold C. Kuhn, Jens H. Viruses Communication Filoviruses, such as Ebola virus and Marburg virus, are of significant human health concern. From 2013 to 2016, Ebola virus caused 11,323 fatalities in Western Africa. Since 2018, two Ebola virus disease outbreaks in the Democratic Republic of the Congo resulted in 2354 fatalities. Although there is progress in medical countermeasure (MCM) development (in particular, vaccines and antibody-based therapeutics), the need for efficacious small-molecule therapeutics remains unmet. Here we describe a novel high-throughput screening assay to identify inhibitors of Ebola virus VP40 matrix protein association with viral particle assembly sites on the interior of the host cell plasma membrane. Using this assay, we screened nearly 3000 small molecules and identified several molecules with the desired inhibitory properties. In secondary assays, one identified compound, sangivamycin, inhibited not only Ebola viral infectivity but also that of other viruses. This finding indicates that it is possible for this new VP40-based screening method to identify highly potent MCMs against Ebola virus and its relatives. MDPI 2020-12-31 /pmc/articles/PMC7824103/ /pubmed/33396288 http://dx.doi.org/10.3390/v13010052 Text en © 2020 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 | Communication Bennett, Ryan P. Finch, Courtney L. Postnikova, Elena N. Stewart, Ryan A. Cai, Yingyun Yu, Shuiqing Liang, Janie Dyall, Julie Salter, Jason D. Smith, Harold C. Kuhn, Jens H. A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title | A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title_full | A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title_fullStr | A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title_full_unstemmed | A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title_short | A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures |
title_sort | novel ebola virus vp40 matrix protein-based screening for identification of novel candidate medical countermeasures |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824103/ https://www.ncbi.nlm.nih.gov/pubmed/33396288 http://dx.doi.org/10.3390/v13010052 |
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