Effects of cellular membranes and the precore protein on hepatitis B virus core particle assembly and DNA replication

Hepatitis B virus (HBV) is an important human pathogen that chronically infects 254 million people in the world. This virus contains a core particle, which plays an important role in the transport and replication of the viral DNA genome. The major protein constituent of this particle is the viral core protein. In this report, we examined how the subcellular compartments and the related precore protein might affect the core particle structure and viral DNA replication. We found that the subcellular localizations could affect the core particle assembly, and membranes and the precore protein could regulate HBV DNA replication. We also found that the inhibition of autophagic degradation increased the precore protein level, suggesting a role of autophagy in the regulation of precore protein activities. These findings provided important information for further understanding the HBV life cycle, which will aid in the development of novel drugs for the treatment of HBV patients.

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Publication Details

Journal
mBio
Published
2025-03-05
DOI
https://doi.org/10.1128/mbio.03972-24
Citations
3
Primary Topic
Hepatitis B Virus Studies
Type
article
Field-Weighted Citation Impact
4.06

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article

Effects of cellular membranes and the precore protein on hepatitis B virus core particle assembly and DNA replication

Jing‐hsiung James Ou, Yu-Chen Chuang
3 citations
mBio
Hepatitis B Virus Studies
4.06
article

Effects of cellular membranes and the precore protein on hepatitis B virus core particle assembly and DNA replication

Jing‐hsiung James Ou, Yu-Chen Chuang
article en
3 citations

Abstract

Hepatitis B virus (HBV) is an important human pathogen that chronically infects 254 million people in the world. This virus contains a core particle, which plays an important role in the transport and replication of the viral DNA genome. The major protein constituent of this particle is the viral core protein. In this report, we examined how the subcellular compartments and the related precore protein might affect the core particle structure and viral DNA replication. We found that the subcellular localizations could affect the core particle assembly, and membranes and the precore protein could regulate HBV DNA replication. We also found that the inhibition of autophagic degradation increased the precore protein level, suggesting a role of autophagy in the regulation of precore protein activities. These findings provided important information for further understanding the HBV life cycle, which will aid in the development of novel drugs for the treatment of HBV patients.

mBioVol. 16(4)
University of Southern California (US)
National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 7%
Hepatitis B Virus Studies
4.06
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