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High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus
The recent development of a Hepatitis C virus (HCV) infectious virus cell culture model system has facilitated the development of whole-virus screening assays which can be used to interrogate the entire virus life cycle. Here, we describe the development of an HCV growth assay capable of identifying...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412796/ https://www.ncbi.nlm.nih.gov/pubmed/22880053 http://dx.doi.org/10.1371/journal.pone.0042609 |
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author | Wichroski, Michael J. Fang, Jie Eggers, Betsy J. Rose, Ronald E. Mazzucco, Charles E. Pokornowski, Kevin A. Baldick, Carl J. Anthony, Monique N. Dowling, Craig J. Barber, Lauren E. Leet, John E. Beno, Brett R. Gerritz, Samuel W. Agler, Michele L. Cockett, Mark I. Tenney, Daniel J. |
author_facet | Wichroski, Michael J. Fang, Jie Eggers, Betsy J. Rose, Ronald E. Mazzucco, Charles E. Pokornowski, Kevin A. Baldick, Carl J. Anthony, Monique N. Dowling, Craig J. Barber, Lauren E. Leet, John E. Beno, Brett R. Gerritz, Samuel W. Agler, Michele L. Cockett, Mark I. Tenney, Daniel J. |
author_sort | Wichroski, Michael J. |
collection | PubMed |
description | The recent development of a Hepatitis C virus (HCV) infectious virus cell culture model system has facilitated the development of whole-virus screening assays which can be used to interrogate the entire virus life cycle. Here, we describe the development of an HCV growth assay capable of identifying inhibitors against all stages of the virus life cycle with assay throughput suitable for rapid screening of large-scale chemical libraries. Novel features include, 1) the use of an efficiently-spreading, full-length, intergenotypic chimeric reporter virus with genotype 1 structural proteins, 2) a homogenous assay format compatible with miniaturization and automated liquid-handling, and 3) flexible assay end-points using either chemiluminescence (high-throughput screening) or Cellomics ArrayScan™ technology (high-content screening). The assay was validated using known HCV antivirals and through a large-scale, high-throughput screening campaign that identified novel and selective entry, replication and late-stage inhibitors. Selection and characterization of resistant viruses provided information regarding inhibitor target and mechanism. Leveraging results from this robust whole-virus assay represents a critical first step towards identifying inhibitors of novel targets to broaden the spectrum of antivirals for the treatment of HCV. |
format | Online Article Text |
id | pubmed-3412796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34127962012-08-09 High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus Wichroski, Michael J. Fang, Jie Eggers, Betsy J. Rose, Ronald E. Mazzucco, Charles E. Pokornowski, Kevin A. Baldick, Carl J. Anthony, Monique N. Dowling, Craig J. Barber, Lauren E. Leet, John E. Beno, Brett R. Gerritz, Samuel W. Agler, Michele L. Cockett, Mark I. Tenney, Daniel J. PLoS One Research Article The recent development of a Hepatitis C virus (HCV) infectious virus cell culture model system has facilitated the development of whole-virus screening assays which can be used to interrogate the entire virus life cycle. Here, we describe the development of an HCV growth assay capable of identifying inhibitors against all stages of the virus life cycle with assay throughput suitable for rapid screening of large-scale chemical libraries. Novel features include, 1) the use of an efficiently-spreading, full-length, intergenotypic chimeric reporter virus with genotype 1 structural proteins, 2) a homogenous assay format compatible with miniaturization and automated liquid-handling, and 3) flexible assay end-points using either chemiluminescence (high-throughput screening) or Cellomics ArrayScan™ technology (high-content screening). The assay was validated using known HCV antivirals and through a large-scale, high-throughput screening campaign that identified novel and selective entry, replication and late-stage inhibitors. Selection and characterization of resistant viruses provided information regarding inhibitor target and mechanism. Leveraging results from this robust whole-virus assay represents a critical first step towards identifying inhibitors of novel targets to broaden the spectrum of antivirals for the treatment of HCV. Public Library of Science 2012-08-06 /pmc/articles/PMC3412796/ /pubmed/22880053 http://dx.doi.org/10.1371/journal.pone.0042609 Text en © 2012 Wichroski et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wichroski, Michael J. Fang, Jie Eggers, Betsy J. Rose, Ronald E. Mazzucco, Charles E. Pokornowski, Kevin A. Baldick, Carl J. Anthony, Monique N. Dowling, Craig J. Barber, Lauren E. Leet, John E. Beno, Brett R. Gerritz, Samuel W. Agler, Michele L. Cockett, Mark I. Tenney, Daniel J. High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title | High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title_full | High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title_fullStr | High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title_full_unstemmed | High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title_short | High-Throughput Screening and Rapid Inhibitor Triage Using an Infectious Chimeric Hepatitis C Virus |
title_sort | high-throughput screening and rapid inhibitor triage using an infectious chimeric hepatitis c virus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412796/ https://www.ncbi.nlm.nih.gov/pubmed/22880053 http://dx.doi.org/10.1371/journal.pone.0042609 |
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