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The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection

Many people worldwide suffer from hepatitis C virus (HCV) infection, which is frequently persistent. The lack of efficient vaccines against HCV and the unavailability of or limited compliance with existing antiviral therapies is problematic for health care systems worldwide. Improved small animal mo...

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Autores principales: Röhrs, Susanne, Begeman, Lineke, Straub, Beate K., Boadella, Mariana, Hanke, Dennis, Wernike, Kerstin, Drewes, Stephan, Hoffmann, Bernd, Keller, Markus, Drexler, Jan Felix, Drosten, Christian, Höper, Dirk, Kuiken, Thijs, Ulrich, Rainer G., Beer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708279/
https://www.ncbi.nlm.nih.gov/pubmed/34960690
http://dx.doi.org/10.3390/v13122421
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author Röhrs, Susanne
Begeman, Lineke
Straub, Beate K.
Boadella, Mariana
Hanke, Dennis
Wernike, Kerstin
Drewes, Stephan
Hoffmann, Bernd
Keller, Markus
Drexler, Jan Felix
Drosten, Christian
Höper, Dirk
Kuiken, Thijs
Ulrich, Rainer G.
Beer, Martin
author_facet Röhrs, Susanne
Begeman, Lineke
Straub, Beate K.
Boadella, Mariana
Hanke, Dennis
Wernike, Kerstin
Drewes, Stephan
Hoffmann, Bernd
Keller, Markus
Drexler, Jan Felix
Drosten, Christian
Höper, Dirk
Kuiken, Thijs
Ulrich, Rainer G.
Beer, Martin
author_sort Röhrs, Susanne
collection PubMed
description Many people worldwide suffer from hepatitis C virus (HCV) infection, which is frequently persistent. The lack of efficient vaccines against HCV and the unavailability of or limited compliance with existing antiviral therapies is problematic for health care systems worldwide. Improved small animal models would support further hepacivirus research, including development of vaccines and novel antivirals. The recent discovery of several mammalian hepaciviruses may facilitate such research. In this study, we demonstrated that bank voles (Clethrionomys glareolus) were susceptible to bank vole-associated Hepacivirus F and Hepacivirus J strains, based on the detection of hepaciviral RNA in 52 of 55 experimentally inoculated voles. In contrast, interferon α/β receptor deficient C57/Bl6 mice were resistant to infection with both bank vole hepaciviruses (BvHVs). The highest viral genome loads in infected voles were detected in the liver, and viral RNA was visualized by in situ hybridization in hepatocytes, confirming a marked hepatotropism. Furthermore, liver lesions in infected voles resembled those of HCV infection in humans. In conclusion, infection with both BvHVs in their natural hosts shares striking similarities to HCV infection in humans and may represent promising small animal models for this important human disease.
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spelling pubmed-87082792021-12-25 The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection Röhrs, Susanne Begeman, Lineke Straub, Beate K. Boadella, Mariana Hanke, Dennis Wernike, Kerstin Drewes, Stephan Hoffmann, Bernd Keller, Markus Drexler, Jan Felix Drosten, Christian Höper, Dirk Kuiken, Thijs Ulrich, Rainer G. Beer, Martin Viruses Article Many people worldwide suffer from hepatitis C virus (HCV) infection, which is frequently persistent. The lack of efficient vaccines against HCV and the unavailability of or limited compliance with existing antiviral therapies is problematic for health care systems worldwide. Improved small animal models would support further hepacivirus research, including development of vaccines and novel antivirals. The recent discovery of several mammalian hepaciviruses may facilitate such research. In this study, we demonstrated that bank voles (Clethrionomys glareolus) were susceptible to bank vole-associated Hepacivirus F and Hepacivirus J strains, based on the detection of hepaciviral RNA in 52 of 55 experimentally inoculated voles. In contrast, interferon α/β receptor deficient C57/Bl6 mice were resistant to infection with both bank vole hepaciviruses (BvHVs). The highest viral genome loads in infected voles were detected in the liver, and viral RNA was visualized by in situ hybridization in hepatocytes, confirming a marked hepatotropism. Furthermore, liver lesions in infected voles resembled those of HCV infection in humans. In conclusion, infection with both BvHVs in their natural hosts shares striking similarities to HCV infection in humans and may represent promising small animal models for this important human disease. MDPI 2021-12-03 /pmc/articles/PMC8708279/ /pubmed/34960690 http://dx.doi.org/10.3390/v13122421 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Röhrs, Susanne
Begeman, Lineke
Straub, Beate K.
Boadella, Mariana
Hanke, Dennis
Wernike, Kerstin
Drewes, Stephan
Hoffmann, Bernd
Keller, Markus
Drexler, Jan Felix
Drosten, Christian
Höper, Dirk
Kuiken, Thijs
Ulrich, Rainer G.
Beer, Martin
The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title_full The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title_fullStr The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title_full_unstemmed The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title_short The Bank Vole (Clethrionomys glareolus)—Small Animal Model for Hepacivirus Infection
title_sort bank vole (clethrionomys glareolus)—small animal model for hepacivirus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708279/
https://www.ncbi.nlm.nih.gov/pubmed/34960690
http://dx.doi.org/10.3390/v13122421
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