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.2018.02.175Additional 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.