Despite this kinship to retroviruses there are fundamental differences beyond the fact that hepadnavirions contain dna instead of rna. Though the liver is the most effective cell type for replicating hbv other extrahepatic sites have been found to be able to support replication to a lesser degree. Attachment the virus gains entry into the cell by binding to receptors on the surface of the cell and entering it by endocytosis mediated by either clathrin or caveolin 1.
The hepatitis b virus as in the case of all other viruses must first attach specifically onto a cell capable of supporting its replication. Cccdna to amplify a viral rna intermediate which is then reverse transcribed back to viral dna. Rcdna is converted to a molecular template dna covalently closed circular dna.
New insight on hepatitis b virus persistence from the study of intrahepatic viral cccdna. Hepatitis b virus hbv specifically infects hepatocytes and causes severe liver diseases. Hepatitis b virus replication is cell cycle independent during liver regeneration in transgenic mice.
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Hepatitis b virus replication cycle. The life cycle of hepatitis b virus is complex. Hepadnaviruses including human hepatitis b virus hbv replicate through reverse transcription of an rna intermediate the pregenomic rna pgrna. Hepatitis b is one of a few known non retroviral viruses which use reverse transcription as a part of its replication process..
The hbv life cycle is unique in that the genomic dna relaxed circular partially double stranded dna. Most peculiar is the initiation. The replication cycle of hepatitis b virus 1 reversible and non cell type specific attachment to cell associated heparan sulfate proteoglycans. Hepatitis b virus replication cycle.
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