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Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses

Hepatitis C virus (HCV) and human pegivirus (HPgV or GB virus C) are globally distributed and infect 2 to 5% of the human population. The lack of tractable-animal models for these viruses, in particular for HCV, has hampered the study of infection, transmission, virulence, immunity, and pathogenesis...

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Autores principales: Kapoor, Amit, Simmonds, Peter, Scheel, Troels K. H., Hjelle, Brian, Cullen, John M., Burbelo, Peter D., Chauhan, Lokendra V., Duraisamy, Raja, Sanchez Leon, Maria, Jain, Komal, Vandegrift, Kurt Jason, Calisher, Charles H., Rice, Charles M., Lipkin, W. Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622934/
https://www.ncbi.nlm.nih.gov/pubmed/23572554
http://dx.doi.org/10.1128/mBio.00216-13
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author Kapoor, Amit
Simmonds, Peter
Scheel, Troels K. H.
Hjelle, Brian
Cullen, John M.
Burbelo, Peter D.
Chauhan, Lokendra V.
Duraisamy, Raja
Sanchez Leon, Maria
Jain, Komal
Vandegrift, Kurt Jason
Calisher, Charles H.
Rice, Charles M.
Lipkin, W. Ian
author_facet Kapoor, Amit
Simmonds, Peter
Scheel, Troels K. H.
Hjelle, Brian
Cullen, John M.
Burbelo, Peter D.
Chauhan, Lokendra V.
Duraisamy, Raja
Sanchez Leon, Maria
Jain, Komal
Vandegrift, Kurt Jason
Calisher, Charles H.
Rice, Charles M.
Lipkin, W. Ian
author_sort Kapoor, Amit
collection PubMed
description Hepatitis C virus (HCV) and human pegivirus (HPgV or GB virus C) are globally distributed and infect 2 to 5% of the human population. The lack of tractable-animal models for these viruses, in particular for HCV, has hampered the study of infection, transmission, virulence, immunity, and pathogenesis. To address this challenge, we searched for homologous viruses in small mammals, including wild rodents. Here we report the discovery of several new hepaciviruses (HCV-like viruses) and pegiviruses (GB virus-like viruses) that infect wild rodents. Complete genome sequences were acquired for a rodent hepacivirus (RHV) found in Peromyscus maniculatus and a rodent pegivirus (RPgV) found in Neotoma albigula. Unique genomic features and phylogenetic analyses confirmed that these RHV and RPgV variants represent several novel virus species in the Hepacivirus and Pegivirus genera within the family Flaviviridae. The genetic diversity of the rodent hepaciviruses exceeded that observed for hepaciviruses infecting either humans or non-primates, leading to new insights into the origin, evolution, and host range of hepaciviruses. The presence of genes, encoded proteins, and translation elements homologous to those found in human hepaciviruses and pegiviruses suggests the potential for the development of new animal systems with which to model HCV pathogenesis, vaccine design, and treatment.
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spelling pubmed-36229342013-04-12 Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses Kapoor, Amit Simmonds, Peter Scheel, Troels K. H. Hjelle, Brian Cullen, John M. Burbelo, Peter D. Chauhan, Lokendra V. Duraisamy, Raja Sanchez Leon, Maria Jain, Komal Vandegrift, Kurt Jason Calisher, Charles H. Rice, Charles M. Lipkin, W. Ian mBio Research Article Hepatitis C virus (HCV) and human pegivirus (HPgV or GB virus C) are globally distributed and infect 2 to 5% of the human population. The lack of tractable-animal models for these viruses, in particular for HCV, has hampered the study of infection, transmission, virulence, immunity, and pathogenesis. To address this challenge, we searched for homologous viruses in small mammals, including wild rodents. Here we report the discovery of several new hepaciviruses (HCV-like viruses) and pegiviruses (GB virus-like viruses) that infect wild rodents. Complete genome sequences were acquired for a rodent hepacivirus (RHV) found in Peromyscus maniculatus and a rodent pegivirus (RPgV) found in Neotoma albigula. Unique genomic features and phylogenetic analyses confirmed that these RHV and RPgV variants represent several novel virus species in the Hepacivirus and Pegivirus genera within the family Flaviviridae. The genetic diversity of the rodent hepaciviruses exceeded that observed for hepaciviruses infecting either humans or non-primates, leading to new insights into the origin, evolution, and host range of hepaciviruses. The presence of genes, encoded proteins, and translation elements homologous to those found in human hepaciviruses and pegiviruses suggests the potential for the development of new animal systems with which to model HCV pathogenesis, vaccine design, and treatment. American Society of Microbiology 2013-04-09 /pmc/articles/PMC3622934/ /pubmed/23572554 http://dx.doi.org/10.1128/mBio.00216-13 Text en Copyright © 2013 Kapoor et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported (http://creativecommons.org/licenses/by-nc-sa/3.0/) license, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kapoor, Amit
Simmonds, Peter
Scheel, Troels K. H.
Hjelle, Brian
Cullen, John M.
Burbelo, Peter D.
Chauhan, Lokendra V.
Duraisamy, Raja
Sanchez Leon, Maria
Jain, Komal
Vandegrift, Kurt Jason
Calisher, Charles H.
Rice, Charles M.
Lipkin, W. Ian
Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title_full Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title_fullStr Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title_full_unstemmed Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title_short Identification of Rodent Homologs of Hepatitis C Virus and Pegiviruses
title_sort identification of rodent homologs of hepatitis c virus and pegiviruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622934/
https://www.ncbi.nlm.nih.gov/pubmed/23572554
http://dx.doi.org/10.1128/mBio.00216-13
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