Hepatitis B virus entry, assembly, and egress

被引:3
作者
Chuang, Yu-Chen [1 ]
Ou, J. -H. James [1 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90007 USA
基金
美国国家卫生研究院;
关键词
hepatitis B virus; viral entry; clathrin-mediated endocytosis; autophagy; multivesicular bodies; exocytosis; amphisomes; hepatitis delta virus; hepatitis C virus; LIVER PLASMA-MEMBRANES; NUCLEAR EXPORT SIGNAL; C VIRUS; DELTA-VIRUS; ENVELOPE PROTEIN; LOW-DENSITY; APOLIPOPROTEIN-E; X PROTEIN; CYSTEINE RESIDUES; DEPENDENT BINDING;
D O I
10.1128/mmbr.00014-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis B virus (HBV) is an important human pathogen that chronically infects approximately 250 million people in the world, resulting in similar to 1 million deaths annually. This virus is a hepatotropic virus and can cause severe liver diseases including cirrhosis and hepatocellular carcinoma. The entry of HBV into hepatocytes is initiated by the interaction of its envelope proteins with its receptors. This is followed by the delivery of the viral nucleocapsid to the nucleus for the release of its genomic DNA and the transcription of viral RNAs. The assembly of the viral capsid particles may then take place in the nucleus or the cytoplasm and may involve cellular membranes. This is followed by the egress of the virus from infected cells. In recent years, significant research progresses had been made toward understanding the entry, the assembly, and the egress of HBV particles. In this review, we discuss the molecular pathways of these processes and compare them with those used by hepatitis delta virus and hepatitis C virus , two other hepatotropic viruses that are also enveloped. The understanding of these processes will help us to understand how HBV replicates and causes diseases, which will help to improve the treatments for HBV patients.
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页数:24
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