| Literature DB >> 32360949 |
Julie Lucifora1, Marion Delphin2.
Abstract
Hepatitis B Virus (HBV) that infects liver parenchymal cells is responsible for severe liver diseases and co-infection with Hepatitis Delta Virus (HDV) leads to the most aggressive form of viral hepatitis. Even tough being different for their viral genome (relaxed circular partially double stranded DNA for HBV and circular RNA for HDV), HBV and HDV are both maintained as episomes in the nucleus of infected cells and use the cellular machinery for the transcription of their viral RNAs. We propose here an update on the current knowledge on HDV replication cycle that may eventually help to identify new antiviral targets.Entities:
Keywords: Episome; Hepatitis B virus (HBV); Hepatitis delta virus (HDV); Hepatocyte; Life cycle
Mesh:
Year: 2020 PMID: 32360949 DOI: 10.1016/j.antiviral.2020.104812
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970