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Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies
Isolation and self-replication of infectious HCV has been a difficult task. However, this is needed for the purposes of developing rational drugs and for the analysis of the natural virus. Our recent report of an in vitro system for the isolation of human HCV from infected patients and their replica...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1609102/ https://www.ncbi.nlm.nih.gov/pubmed/17010197 http://dx.doi.org/10.1186/1743-422X-3-81 |
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author | Revie, Dennis Alberti, Michael O Braich, Ravi S Chelyapov, Nickolas Bayles, David Prichard, John G Salahuddin, S Zaki |
author_facet | Revie, Dennis Alberti, Michael O Braich, Ravi S Chelyapov, Nickolas Bayles, David Prichard, John G Salahuddin, S Zaki |
author_sort | Revie, Dennis |
collection | PubMed |
description | Isolation and self-replication of infectious HCV has been a difficult task. However, this is needed for the purposes of developing rational drugs and for the analysis of the natural virus. Our recent report of an in vitro system for the isolation of human HCV from infected patients and their replication in tissue culture addresses this challenge. At California Institute of Molecular Medicine several isolates of HCV, called CIMM-HCV, were grown for over three years in cell culture. This is a report of the analysis of CIMM-HCV isolates for subtypes and quasispecies using a 269 bp segment of the 5'UTR. HCV RNA from three patients and eleven CIMM-HCV were analyzed for this purpose. All isolates were essentially identical. Isolates of HCV from one patient were serially transmitted into fresh cells up to eight times and the progeny viruses from each transmission were compared to each other and also to the primary isolates from the patient's serum. Some isolates were also transmitted to different cell types, while others were cultured continuously without retransmission for over three years. We noted minor sequence changes when HCV was cultured for extended periods of time. HCV in T-cells and non-committed lymphoid cells showed a few differences when compared to isolates obtained from immortalized B-cells. These viruses maintained close similarity despite repeated transmissions and passage of time. There were no subtypes or quasispecies noted in CIMM-HCV. |
format | Text |
id | pubmed-1609102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16091022006-10-14 Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies Revie, Dennis Alberti, Michael O Braich, Ravi S Chelyapov, Nickolas Bayles, David Prichard, John G Salahuddin, S Zaki Virol J Research Isolation and self-replication of infectious HCV has been a difficult task. However, this is needed for the purposes of developing rational drugs and for the analysis of the natural virus. Our recent report of an in vitro system for the isolation of human HCV from infected patients and their replication in tissue culture addresses this challenge. At California Institute of Molecular Medicine several isolates of HCV, called CIMM-HCV, were grown for over three years in cell culture. This is a report of the analysis of CIMM-HCV isolates for subtypes and quasispecies using a 269 bp segment of the 5'UTR. HCV RNA from three patients and eleven CIMM-HCV were analyzed for this purpose. All isolates were essentially identical. Isolates of HCV from one patient were serially transmitted into fresh cells up to eight times and the progeny viruses from each transmission were compared to each other and also to the primary isolates from the patient's serum. Some isolates were also transmitted to different cell types, while others were cultured continuously without retransmission for over three years. We noted minor sequence changes when HCV was cultured for extended periods of time. HCV in T-cells and non-committed lymphoid cells showed a few differences when compared to isolates obtained from immortalized B-cells. These viruses maintained close similarity despite repeated transmissions and passage of time. There were no subtypes or quasispecies noted in CIMM-HCV. BioMed Central 2006-09-29 /pmc/articles/PMC1609102/ /pubmed/17010197 http://dx.doi.org/10.1186/1743-422X-3-81 Text en Copyright © 2006 Revie et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Revie, Dennis Alberti, Michael O Braich, Ravi S Chelyapov, Nickolas Bayles, David Prichard, John G Salahuddin, S Zaki Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title | Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title_full | Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title_fullStr | Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title_full_unstemmed | Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title_short | Analysis of in vitro replicated human hepatitis C virus (HCV) for the determination of genotypes and quasispecies |
title_sort | analysis of in vitro replicated human hepatitis c virus (hcv) for the determination of genotypes and quasispecies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1609102/ https://www.ncbi.nlm.nih.gov/pubmed/17010197 http://dx.doi.org/10.1186/1743-422X-3-81 |
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