Viral Hepatitis
Copyright ©2007 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 28, 2007; 13(40): 5324-5330
Published online Oct 28, 2007. doi: 10.3748/wjg.v13.i40.5324
Establishment and primary application of a mouse model with hepatitis B virus replication
Feng-Jun Liu, Li Liu, Fang He, Su Wang, Tao-You Zhou, Cong Liu, Lin-Yu Deng, Hong Tang
Feng-Jun Liu, Li Liu, Fang He, Su Wang, Tao-You Zhou, Cong Liu, Hong Tang, Center of Infectious Diseases, Division of Molecular Biology of Infectious Diseases, National Key Laboratory of Biotherapy (Sichuan University), West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China
Lin-Yu Deng, National Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, Sichuan Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National Science Fund for Distinguished Young Scholars from the National Natural Science Foundation of China, No. 30325036, and a grant from the National Natural Science Foundation of China, No. 30571640
Correspondence to: Professor Hong Tang, Center of Infectious Diseases, Division of Molecular Biology of infectious Diseases, National Key Laboratory of Biotherapy (Sichuan University), West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China. htang6198@hotmail.com
Telephone: +86-28-85422650 Fax: +86-28-85423052
Received: March 29, 2007
Revised: May 24, 2007
Accepted: August 14, 2007
Published online: October 28, 2007
Abstract

AIM: To establish a rapid and convenient animal model with hepatitis B virus (HBV) replication.

METHODS: A naked DNA solution of HBV-replication-competent plasmid was transferred to BALB/C mice via the tail vein, using a hydrodynamic in vivo transfection procedure. After injection, these mice were sacrificed on d 1, 3, 4, 5, 7 and 10. HBV DNA replication intermediates in the liver were analyzed by Southern blot hybridization. The expression of hepatitis B core antigen (HBcAg) and hepatitis B surface antigen (HBsAg) in the liver was checked by immunohistochemistry. Serum HBsAg and hepatitis B e antigen (HBeAg) was detected by enzyme-linked immunosorbent assay (ELISA). Inhibition of HBV replication was compared in HBV replication model mice treated intraperitoneally with polyinosinic-polytidylin acid (polyIC) or phosphate-buffered saline (PBS).

RESULTS: After hydrodynamic in vivo transfection, HBV DNA replication intermediates in the mouse liver were detectable on d 1 and abundant on d 3 and 4, the levels were slightly decreased and remained relatively stable between d 5 and 7, and were almost undetectable on d 10. The expression patterns of HBcAg and HBsAg were similar to that of HBV replication intermediate DNA, except that they reached a peak on d 1 after injection. No obvious differences in HBV DNA replication intermediates were observed in the left, right and middle lobes of the liver. After treatment with polyIC, the level of HBV intermediate DNA in the liver was lower than that in the control mice injected with PBS.

CONCLUSION: A rapid and convenient mouse model with a high level of HBV replication was developed and used to investigate the inhibitory effect of polyIC on HBV replication, which provides a useful tool for future functional studies of the HBV genome.

Keywords: Animal model; Gene expression; Hepatitis B Virus; Hydrodynamic transfection; Polyinosinic-polytidylin acid; Virus replication