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Morphogenesis of hepatitis B virus and its subviral envelope particles
Author(s) -
Patient Romuald,
Hourioux Christophe,
Roingeard Philippe
Publication year - 2009
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/j.1462-5822.2009.01363.x
Subject(s) - biology , viral envelope , virology , lytic cycle , morphogenesis , hepatitis b virus , microbiology and biotechnology , virus , budding , intracellular , viral replication , golgi apparatus , hepatitis b virus pre beta , genetics , hepatitis b virus dna polymerase , gene , endoplasmic reticulum
Summary After cell hijacking and intracellular amplification, non‐lytic enveloped viruses are usually released from the infected cell by budding across internal membranes or through the plasma membrane. The enveloped human hepatitis B virus (HBV) is an example of virus using an intracellular compartment to form new virions. Four decades after its discovery, HBV is still the primary cause of death by cancer due to a viral infection worldwide. Despite numerous studies on HBV genome replication little is known about its morphogenesis process. In addition to viral neogenesis, the HBV envelope proteins have the capability without any other viral component to form empty subviral envelope particles (SVPs), which are secreted into the blood of infected patients. A better knowledge of this process may be critical for future antiviral strategies. Previous studies have speculated that the morphogenesis of HBV and its SVPs occur through the same mechanisms. However, recent data clearly suggest that two different processes, including constitutive Golgi pathway or cellular machinery that generates internal vesicles of multivesicular bodies (MVB), independently form these two viral entities.

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