Published March 2018 | Version v1
Journal article

Novel stable HBV producing cell line systems for expression and screening antiviral inhibitor of hepatitis B virus in human hepatoma cell line

  • 1. Central Pharmaceutical Research Institute, Japan Tobacco Inc, Osaka, 569-1125 (Japan)
  • 2. Department of Virology II, National Institute of Infectious Diseases, Tokyo, 162-8640 (Japan)
  • 3. Digestive Diseases Center, Showa University Koto-Toyosu Hospital, Tokyo, 135-8577 (Japan)

Description

Highlights: • Novel HBV clones with high replication activities were identified from the sera of patients with chronic HBV. • Novel stable cell lines showed HBV replication activities and were susceptible to several antiviral inhibitors. • Novel stable cell lines are valuable tools for analyzing viral phenotypes in vitro and for screening antiviral agents. Chronic hepatitis B virus (HBV) infection is currently a major public health burden. Therefore, there is an urgent need for the development of novel antiviral inhibitors. The stable HBV-producing cell lines of genotype D are widely used to investigate the HBV life cycle and to evaluate antiviral agents. However, stable HBV-producing cell lines of different genotypes do not exist. To construct more convenient and efficient novel cell systems, stable cell lines of genotypes A, B, and C were established using a full-length HBV genome sequence isolated from chronic HBV patients in human hepatoma HepG2 cells. Novel HBV clones were identified and stable HBV-producing cell lines derived from these clones were constructed. HBV replication activities demonstrated time-dependent expression, and the novel cell lines were susceptible to several antiviral inhibitors with no cytotoxicity. Furthermore, infectious viruses were produced from these cell lines. In conclusion, we have established novel stable HBV-producing cell line systems of genotypes A, B, and C. These systems can provide valuable tools for screening antiviral agents and analyzing viral phenotypes in vitro.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2018.02.175

Additional details

Identifiers

DOI
10.1016/j.bbrc.2018.02.175;
PII
S0006291X18304157;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
498
Journal Issue
1
Journal Page Range
p. 64-71
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53054504
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
GENOTYPE; HEPATITIS; HEPATOMAS; PHENOTYPE; PUBLIC HEALTH; TOXICITY; VIRUSES
Descriptors DEC
CARCINOMAS; DIGESTIVE SYSTEM DISEASES; DISEASES; MICROORGANISMS; NEOPLASMS; PARASITES

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.