Persistent hepatitis B viral replication in a FVB/N mouse model: impact of host and viral factors

• Published in: PloS one 2012-05, Vol.7 (5), p.e36984-e36984
• Main Authors: Chen, Shih-Hui, Wu, Hui-Lin, Kao, Jia-Horng, Hwang, Lih-Hwa
• Format: Article
• Language: English
• Subjects: Adenoviruses; Alanine; Alanine transaminase; Alanine Transaminase - genetics; Alanine Transaminase - immunology; Alanine Transaminase - metabolism; Analysis; Animals; Antigens; Biological response modifiers; Biology; Chemokine CXCL10 - genetics; Chemokine CXCL10 - immunology; Chemokine CXCL10 - metabolism; Chemokine CXCL9 - genetics; Chemokine CXCL9 - immunology; Chemokine CXCL9 - metabolism; Chemokines; Cloning; CXCL10 protein; Cytotoxicity; Deoxyribonucleic acid; DNA; DNA Replication - genetics; DNA Replication - immunology; Flow cytometry; Genomes; Health aspects; Hepatitis; Hepatitis B; Hepatitis B - genetics; Hepatitis B - immunology; Hepatitis B - metabolism; Hepatitis B - virology; Hepatitis B Surface Antigens - genetics; Hepatitis B Surface Antigens - immunology; Hepatitis B Surface Antigens - metabolism; Hepatitis B virus - genetics; Hepatitis B virus - immunology; Hepatitis B virus - physiology; Host-Pathogen Interactions; House mouse; Immune clearance; Immune response; Immunology; Infection; Infections; Inflammation; Inflammation - genetics; Inflammation - immunology; Inflammation - metabolism; Inflammation - virology; Injection; Interferon; Interferon-gamma - genetics; Interferon-gamma - immunology; Interferon-gamma - metabolism; Liver; Liver - immunology; Liver - metabolism; Liver - virology; Liver cancer; Lymphocytes; Lymphocytes T; Male; Medicine; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mutation; Replication; Reverse transcription; Rodents; T cells; T-Lymphocytes, Cytotoxic - immunology; T-Lymphocytes, Cytotoxic - metabolism; Transcription (Genetics); Tumor Necrosis Factor-alpha - genetics; Tumor Necrosis Factor-alpha - immunology; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-TNF; Tumor necrosis factor-α; Vectors (Biology); Virus replication; Virus Replication - genetics; Virus Replication - immunology; Viruses; γ-Interferon
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0036984

The mechanism underlying the chronicity of hepatitis B virus (HBV) infection has long been an interesting question. However, this mechanism remains unclear largely due to the lack of an animal model that can support persistent HBV replication and allow for the investigation of the relevant immune responses. In this study, we used hydrodynamic injection to introduce HBV replicon DNA into the livers of three different mouse strains: BALB/c, C57BL/6, and FVB/N. Interestingly, we found that an HBV clone persistently replicated in the livers of FVB/N mice for up to 50 weeks but was rapidly cleared from the livers of BALB/c and C57BL/6 mice. Flow cytometric analysis and quantitative reverse transcription PCR analysis of the mouse livers indicated that after DNA injection, FVB/N mice had few intrahepatic activated cytotoxic T lymphocytes (CTLs) and produced low levels of alanine aminotransferase, interferon (IFN)-γ, tumor necrosis factor (TNF)-α, and the CXCL9 and CXCL10 chemokines. These findings were in sharp contrast with those observed in BALB/c and C57BL/6 mice, reflecting a strong correlation between the degree of liver inflammation and viral clearance. Mutational analysis further demonstrated that a change of Asn-214 to Ser-214 in the HBV surface antigen rendered the persistent HBV clone clearable in FVB/N mice, which was accompanied by increased levels of activated CTL and upregulated expression of IFN-γ, CXCL9, and CXCL10 in the livers. These results indicate that the heterogeneity of the host factors and viral sequences may influence the immune responses against HBV. An inadequate activation of immune or inflammatory responses can lead to persistent HBV replication in vivo.