Abstract

In the hydrodynamic injection (HI) BALB/c mouse model with the overlength viral genome, we have found that woodchuck hepatitis virus (WHV) could persist for a prolonged period of time (up to 45 weeks), while hepatitis B virus (HBV) was mostly cleared at week four. In this study, we constructed a series of chimeric genomes based on HBV and WHV, in which the individual sequences of a 1.3-fold overlength HBV genome in pBS-HBV1.3 were replaced by their counterparts from WHV. After HI with the WHV-HBV chimeric constructs in BALB/c mice, serum viral antigen, viral DNA (vDNA), and intrahepatic viral antigen expression were analyzed to evaluate the persistence of the chimeric genomes. Interestingly, we found that HI with three chimeric WHV-HBV genomes resulted in persistent antigenemia in mice. All of the persistent chimeric genomes contained the preC region and the part of the C region encoding the N-terminal 1–145 amino acids of the WHV genome. These results indicated that the preC region and the N-terminal part of the C region of the WHV genome may play a role in the persistent antigenemia. The chimeric WHV-HBV genomes were able to stably express viral antigens in the liver and could be further used to express hepadnaviral antigens to study their pathogenic potential.

Highlights

  • The hydrodynamic injection (HI) mouse model has been explored in different studies in hepatitisBvirus (HBV) research [1]

  • We created a series of chimeric woodchuck hepatitis virus (WHV)-hepatitis B virus (HBV) genomes based on a commonly used vector and explored hydrodynamic injection of the chimeric plasmids in BALB/c mice to study genomic factors that determine HBV surface antigen (HBsAg) persistence

  • We assume that the vector backbone does not represent a determinant for the persistence of WHV or the chimeric Woodchuck Hepatitis Virus and Hepatitis B Virus (WHV-HBV) genome in the HI mouse model

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Summary

Introduction

The hydrodynamic injection (HI) mouse model has been explored in different studies in hepatitis. HBV replication and HBV surface antigen (HBsAg) expression that persisted for more than six months in approximately 40% of the injected mice [3]. We explored pAAV/HBV1.3 (containing a 1.3-fold overlength HBV genome) in C57BL/6 mice. We speculated that in addition to the backbone of plasmids and the genetic background of the injected specimen, viral characteristics could be an independent determinant for viral replication and persistence in the HI mouse model. WHV and HBV share a remarkable similarity in genome organization and replication strategy [12]. Their nucleotide (nt) sequences were found to have a homology of 62%–70% [13].

Ethics Statement
Serological Assays
Statistical Analysis
Results
Magnification
Persistent
C1819T Mutation in pWHBV5 Led to HBsAg Persistence
Discussion
Full Text
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