Characterization of nonconventional hepatitis B viruses lacking the core promoter

• Published in: Virology (New York, N.Y.) N.Y.), 2004-12, Vol.330 (2), p.437-446
• Main Authors: Chang, Shau-Feng, Chang, Shih-Hsuan, Li, Bi-Chen, Will, Hans, Jürgen Netter, Hans
• Format: Article
• Language: English
• Subjects: Carrier State - virology; Cell Line; DNA, Viral - blood; DNA, Viral - isolation & purification; Gene Expression Regulation, Viral; Hepatitis B Core Antigens - genetics; Hepatitis B virus; Hepatitis B virus - genetics; Hepatitis B virus - isolation & purification; Hepatitis B, Chronic - virology; Humans; Mutant; Polymerase Chain Reaction; Promoter Regions, Genetic; Recombination, Genetic; RNA, Messenger - biosynthesis; RNA, Viral - biosynthesis; Sequence Deletion; Transcription, Genetic; Transfection; Truncated core promoter region; Viral Proteins - biosynthesis
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1016/j.virol.2004.10.001

The core gene (C-gene) promoter and regulatory sequences play a central role in the hepatitis B virus (HBV) life cycle. They are essential for the synthesis of the pregenomic and precore mRNA. The pregenomic RNA is the template required for replication and also the template for the synthesis of the core protein and polymerase. Here, we report the in vivo existence and functional characterization of HBV variants that lack the C-gene promoter region and the regulatory sequences located therein. HBV promoter fragments were isolated by PCR from sera of chronic carriers and characterized. Truncated promoter elements were identified, and then tested in the context of wild-type genomes in the HuH-7 cell line. The expression of the recombinant HBV genome resulted in the synthesis of surface proteins, and low level of core protein as well as a transcript pattern similar to, but smaller in size to wild-type virus. The recombinant HBV genome with the truncated promoter region produced pregenomic RNA-like transcripts. These transcripts were encapsidated and reverse transcribed when complemented by sufficient core and polymerase protein. These date provide an explanation as to why such deletion mutants of HBV can be produced at all, they highlight the functional potentials of viral sequences activated by mutations and may be of relevance for viral evolution and persistence.