Hepatitis B Surface Antigen: A Pivotal Role in the Virus–Host Interactions

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Human Virology and Viral Diseases".

Deadline for manuscript submissions: 30 April 2025 | Viewed by 1739

Special Issue Editors


E-Mail Website
Guest Editor
INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, QC H7V 1B7, Canada
Interests: hepatitis virus; HBV; HCV

E-Mail Website
Guest Editor
INRS-Centre Armand-Frappier Santé Biotechnologie, Laval, QC H7V 1B7, Canada
Interests: hepatitis virus; HBV; HBsAg

Special Issue Information

Dear Colleagues,

Hepatitis B surface antigen (HBsAg), the surface antigen encoded by the hepatitis B virus (HBV), is the main component of the viral envelope of HBV but also of its occasional satellite virus, the  Hepatitis Delta virus (HDV). These two human viruses cause chronic infection of the liver, which may lead to severe liver disease, including cirrhosis and hepatocellular carcinoma. The elimination of HBsAg from the blood circulation becomes a main goal for achieving a long-term functional cure in patients.

HBsAg is produced from a single open reading frame that gives rise to three different isoforms that differ in their N-terminal ends, namely, the small (S-HBsAg), the medium (M-HBsAg), and the large (L-HBsAg). In chronically infected individuals, HBsAg is mostly found as part of non-infectious subviral particles (SVPs) composed almost exclusively of S-HBsAg that are in large excess over the infectious HBV virion (Dane particles). Infectious HBV and HDV virions contain the three HBsAg isoforms, where S-HBsAg drives virions morphogenesis and L-HBsAg is essential for the recruitment of the HBV capsid as well as for viral entry into hepatocytes through its direct interaction with the sodium taurocholate co-transporting polypeptide (NTCP) receptor.

In this Special Issue, we welcome any novel works regarding HBsAg translation, maturation, intracellular trafficking, SVP and Dane particle formation and secretion, meaningful HBsAg–host protein interaction, and its involvement in cell entry.

Dr. Patrick Labonte
Dr. Matthieu Blanchet
Guest Editors

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Keywords

  • hepatitis B surface antigen
  • HBsAg
  • HBV
  • HDV

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Published Papers (1 paper)

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Review

17 pages, 4378 KiB  
Review
Unveiling the Molecular Architecture of HBV Spherical Subviral Particles: Structure, Symmetry, and Lipid Dynamics
by Sonal Garg, Alyssa Ochetto, Jianming Hu and Joseph Che-Yen Wang
Viruses 2025, 17(1), 48; https://doi.org/10.3390/v17010048 - 31 Dec 2024
Cited by 1 | Viewed by 1342
Abstract
Since the discovery of the Australia antigen, now known as the hepatitis B surface antigen (HBsAg), significant research has been conducted to elucidate its physical, chemical, structural, and functional properties. Subviral particles (SVPs) containing HBsAg are highly immunogenic, non-infectious entities that have not [...] Read more.
Since the discovery of the Australia antigen, now known as the hepatitis B surface antigen (HBsAg), significant research has been conducted to elucidate its physical, chemical, structural, and functional properties. Subviral particles (SVPs) containing HBsAg are highly immunogenic, non-infectious entities that have not only revolutionized vaccine development but also provided critical insights into HBV immune evasion and viral assembly. Recent advances in cryo-electron microscopy (cryo-EM) have uncovered the heterogeneity and dynamic nature of spherical HBV SVPs, emphasizing the essential role of lipid–protein interactions in maintaining particle stability. In this review, recent progress in understanding the molecular architecture of HBV SVPs is consolidated, focusing on their symmetry, lipid organization, and disassembly–reassembly dynamics. High-resolution structural models reveal unique lipid arrangements that stabilize hydrophobic residues, preserve antigenicity, and contribute to SVP functionality. These findings highlight the significance of hydrophobic interactions and lipid–protein dynamics in HBV SVP assembly and stability, offering valuable perspectives for optimizing SVP-based vaccine platforms and therapeutic strategies. Full article
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