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Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo

The tree shrew (Tupaia belangeri chinensis), a small animal widely distributed in Southeast Asia and southwest China, has the potential to be developed as an animal model for hepatitis C. To determine the susceptibility of the tree shrew to hepatitis C virus (HCV) infection in vitro and in vivo, a w...

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Autores principales: Feng, Yue, Feng, Yue-Mei, Lu, Caixia, Han, Yuanyuan, Liu, Li, Sun, Xiaomei, Dai, Jiejie, Xia, Xueshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656785/
https://www.ncbi.nlm.nih.gov/pubmed/28758632
http://dx.doi.org/10.1099/jgv.0.000869
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author Feng, Yue
Feng, Yue-Mei
Lu, Caixia
Han, Yuanyuan
Liu, Li
Sun, Xiaomei
Dai, Jiejie
Xia, Xueshan
author_facet Feng, Yue
Feng, Yue-Mei
Lu, Caixia
Han, Yuanyuan
Liu, Li
Sun, Xiaomei
Dai, Jiejie
Xia, Xueshan
author_sort Feng, Yue
collection PubMed
description The tree shrew (Tupaia belangeri chinensis), a small animal widely distributed in Southeast Asia and southwest China, has the potential to be developed as an animal model for hepatitis C. To determine the susceptibility of the tree shrew to hepatitis C virus (HCV) infection in vitro and in vivo, a well-established HCV, produced from the J6/JFH1-Huh7.5.1 culture system, was used to infect cultured primary tupaia hepatocytes (PTHs) and tree shrews. The in vitro results showed that HCV genomic RNA and HCV-specific nonstructural protein 5A (NS5A) could be detected in the PTH cell culture from days 3–15 post-infection, although the viral load was lower than that observed in Huh7.5.1 cell culture. The occurrence of five sense mutations [S391A, G397A, L402F and M405T in the hypervariable region 1 (HVR1) of envelope glycoprotein 2 and I2750M in NS5B] suggested that HCV undergoes genetic evolution during culture. Fourteen of the 30 experimental tree shrews (46.7 %) were found to be infected, although the HCV viremia was intermittent in vivo. A positive test for HCV RNA in liver tissue provided stronger evidence for HCV infection and replication in tree shrews. The results of an immunohistochemistry assay also demonstrated the presence of four HCV-specific proteins (Core, E2, NS3/4 and NS5A) in the hepatocytes of infected tree shrews. The pathological changes observed in the liver tissue of infected tree shrews could be considered to be representative symptoms of mild hepatitis. These results revealed that the tree shrew can be used as an animal model supporting the infection and replication of HCV in vitro and in vivo.
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spelling pubmed-56567852017-11-14 Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo Feng, Yue Feng, Yue-Mei Lu, Caixia Han, Yuanyuan Liu, Li Sun, Xiaomei Dai, Jiejie Xia, Xueshan J Gen Virol Research Article The tree shrew (Tupaia belangeri chinensis), a small animal widely distributed in Southeast Asia and southwest China, has the potential to be developed as an animal model for hepatitis C. To determine the susceptibility of the tree shrew to hepatitis C virus (HCV) infection in vitro and in vivo, a well-established HCV, produced from the J6/JFH1-Huh7.5.1 culture system, was used to infect cultured primary tupaia hepatocytes (PTHs) and tree shrews. The in vitro results showed that HCV genomic RNA and HCV-specific nonstructural protein 5A (NS5A) could be detected in the PTH cell culture from days 3–15 post-infection, although the viral load was lower than that observed in Huh7.5.1 cell culture. The occurrence of five sense mutations [S391A, G397A, L402F and M405T in the hypervariable region 1 (HVR1) of envelope glycoprotein 2 and I2750M in NS5B] suggested that HCV undergoes genetic evolution during culture. Fourteen of the 30 experimental tree shrews (46.7 %) were found to be infected, although the HCV viremia was intermittent in vivo. A positive test for HCV RNA in liver tissue provided stronger evidence for HCV infection and replication in tree shrews. The results of an immunohistochemistry assay also demonstrated the presence of four HCV-specific proteins (Core, E2, NS3/4 and NS5A) in the hepatocytes of infected tree shrews. The pathological changes observed in the liver tissue of infected tree shrews could be considered to be representative symptoms of mild hepatitis. These results revealed that the tree shrew can be used as an animal model supporting the infection and replication of HCV in vitro and in vivo. Microbiology Society 2017-08 2017-07-31 /pmc/articles/PMC5656785/ /pubmed/28758632 http://dx.doi.org/10.1099/jgv.0.000869 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Feng, Yue
Feng, Yue-Mei
Lu, Caixia
Han, Yuanyuan
Liu, Li
Sun, Xiaomei
Dai, Jiejie
Xia, Xueshan
Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title_full Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title_fullStr Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title_full_unstemmed Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title_short Tree shrew, a potential animal model for hepatitis C, supports the infection and replication of HCV in vitro and in vivo
title_sort tree shrew, a potential animal model for hepatitis c, supports the infection and replication of hcv in vitro and in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656785/
https://www.ncbi.nlm.nih.gov/pubmed/28758632
http://dx.doi.org/10.1099/jgv.0.000869
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