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Sequence analysis and functional characterization of full-length hepatitis B virus genomes from Korean cirrhotic patients with or without liver cancer.

Authors
 Huailiang Zhou  ;  Dina Gewaily  ;  Sang Hoon Ahn  ;  Carina Preskill  ;  Yongxiang Wang  ;  Li Zong  ;  Jing Zhang  ;  Kwang-Hyub Han  ;  Jack Wands  ;  Jisu Li  ;  Shuping Tong 
Citation
 Virus Research, Vol.235(Special SI) : 86-95, 2017 
Journal Title
 Virus Research 
ISSN
 0168-1702 
Issue Date
2017
MeSH
Asian Continental Ancestry Group ; Cell Line, Tumor ; Genetic Variation* ; Genome, Viral ; Genotype ; Hepatitis B virus/classification ; Hepatitis B virus/genetics* ; Hepatitis B virus/isolation & purification ; Hepatitis B virus/physiology ; Hepatitis B, Chronic/complications ; Hepatitis B, Chronic/virology* ; Humans ; Liver Cirrhosis/complications ; Liver Cirrhosis/virology* ; Liver Neoplasms/virology* ; Mutation* ; Sequence Analysis ; Virus Replication
Keywords
Core promoter mutations ; Genome replication ; Hepatitis B surface antigen ; Hepatitis B virus ; Liver cancer ; PreS deletions
Abstract
This study aimed to identify and characterize mutations in the hepatitis B virus (HBV) genome associated with advanced liver diseases. The 3.2-kb HBV genome of the C2 subgenotype was amplified from sera of 18 cirrhotic Korean patients with (10) or without (8) hepatocellular carcinoma (HCC), and two clones per patient were characterized by transient transfection experiments in human hepatoma cells. While A1762T/G1764A core promoter mutations were highly prevalent in both groups, the G1896A precore mutation to abolish hepatitis B e antigen (HBeAg) expression was more common in HCC clones (55% vs. 20%). High replication capacity was mostly found in HCC clones and associated with core promoter mutations, whereas more non-HCC clones harbored a nonfunctional core gene (34% vs. 8%). Large in-frame deletions in the preS region were found in 60% of HCC clones and 38% of non-HCC clones. They removed the first 11 residues of large envelope protein or impaired small envelope protein expression, or deleted a neutralizing epitope in the preS2 domain. Additional point mutations prevented middle envelope protein expression, or caused nonsense mutations in the preS or S region to truncate large and/or small envelope protein. Consequently, many clones were unable to express or secrete hepatitis B surface antigen (HBsAg). In conclusion, mutations associated with the advanced stage of chronic HBV infection are complex and diverse. Host immune pressure most likely selected for mutations in the HBV genome to abolish or reduce HBeAg or HBsAg production, to enhance genome replication, or to escape neutralizing antibodies. Some of these mutations may contribute to liver cirrhosis or HCC development.
URI
http://ir.ymlib.yonsei.ac.kr/handle/22282913/161722
DOI
10.1016/j.virusres.2017.03.021
Appears in Collections:
1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실)
Yonsei Authors
안상훈(Ahn, Sang Hoon)
한광협(Han, Kwang Hyup)
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Full Text
https://www.sciencedirect.com/science/article/pii/S0168170217301259
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