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Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents
Hepatitis C virus (HCV) is transmitted between hepatocytes via classical cell entry but also uses direct cell-cell transfer to infect neighboring hepatocytes. Viral cell-cell transmission has been shown to play an important role in viral persistence allowing evasion from neutralizing antibodies. In...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022730/ https://www.ncbi.nlm.nih.gov/pubmed/24830295 http://dx.doi.org/10.1371/journal.ppat.1004128 |
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author | Xiao, Fei Fofana, Isabel Heydmann, Laura Barth, Heidi Soulier, Eric Habersetzer, François Doffoël, Michel Bukh, Jens Patel, Arvind H. Zeisel, Mirjam B. Baumert, Thomas F. |
author_facet | Xiao, Fei Fofana, Isabel Heydmann, Laura Barth, Heidi Soulier, Eric Habersetzer, François Doffoël, Michel Bukh, Jens Patel, Arvind H. Zeisel, Mirjam B. Baumert, Thomas F. |
author_sort | Xiao, Fei |
collection | PubMed |
description | Hepatitis C virus (HCV) is transmitted between hepatocytes via classical cell entry but also uses direct cell-cell transfer to infect neighboring hepatocytes. Viral cell-cell transmission has been shown to play an important role in viral persistence allowing evasion from neutralizing antibodies. In contrast, the role of HCV cell-cell transmission for antiviral resistance is unknown. Aiming to address this question we investigated the phenotype of HCV strains exhibiting resistance to direct-acting antivirals (DAAs) in state-of-the-art model systems for cell-cell transmission and spread. Using HCV genotype 2 as a model virus, we show that cell-cell transmission is the main route of viral spread of DAA-resistant HCV. Cell-cell transmission of DAA-resistant viruses results in viral persistence and thus hampers viral eradication. We also show that blocking cell-cell transmission using host-targeting entry inhibitors (HTEIs) was highly effective in inhibiting viral dissemination of resistant genotype 2 viruses. Combining HTEIs with DAAs prevented antiviral resistance and led to rapid elimination of the virus in cell culture model. In conclusion, our work provides evidence that cell-cell transmission plays an important role in dissemination and maintenance of resistant variants in cell culture models. Blocking virus cell-cell transmission prevents emergence of drug resistance in persistent viral infection including resistance to HCV DAAs. |
format | Online Article Text |
id | pubmed-4022730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40227302014-05-21 Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents Xiao, Fei Fofana, Isabel Heydmann, Laura Barth, Heidi Soulier, Eric Habersetzer, François Doffoël, Michel Bukh, Jens Patel, Arvind H. Zeisel, Mirjam B. Baumert, Thomas F. PLoS Pathog Research Article Hepatitis C virus (HCV) is transmitted between hepatocytes via classical cell entry but also uses direct cell-cell transfer to infect neighboring hepatocytes. Viral cell-cell transmission has been shown to play an important role in viral persistence allowing evasion from neutralizing antibodies. In contrast, the role of HCV cell-cell transmission for antiviral resistance is unknown. Aiming to address this question we investigated the phenotype of HCV strains exhibiting resistance to direct-acting antivirals (DAAs) in state-of-the-art model systems for cell-cell transmission and spread. Using HCV genotype 2 as a model virus, we show that cell-cell transmission is the main route of viral spread of DAA-resistant HCV. Cell-cell transmission of DAA-resistant viruses results in viral persistence and thus hampers viral eradication. We also show that blocking cell-cell transmission using host-targeting entry inhibitors (HTEIs) was highly effective in inhibiting viral dissemination of resistant genotype 2 viruses. Combining HTEIs with DAAs prevented antiviral resistance and led to rapid elimination of the virus in cell culture model. In conclusion, our work provides evidence that cell-cell transmission plays an important role in dissemination and maintenance of resistant variants in cell culture models. Blocking virus cell-cell transmission prevents emergence of drug resistance in persistent viral infection including resistance to HCV DAAs. Public Library of Science 2014-05-15 /pmc/articles/PMC4022730/ /pubmed/24830295 http://dx.doi.org/10.1371/journal.ppat.1004128 Text en © 2014 Xiao 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 Xiao, Fei Fofana, Isabel Heydmann, Laura Barth, Heidi Soulier, Eric Habersetzer, François Doffoël, Michel Bukh, Jens Patel, Arvind H. Zeisel, Mirjam B. Baumert, Thomas F. Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title | Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title_full | Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title_fullStr | Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title_full_unstemmed | Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title_short | Hepatitis C Virus Cell-Cell Transmission and Resistance to Direct-Acting Antiviral Agents |
title_sort | hepatitis c virus cell-cell transmission and resistance to direct-acting antiviral agents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022730/ https://www.ncbi.nlm.nih.gov/pubmed/24830295 http://dx.doi.org/10.1371/journal.ppat.1004128 |
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