Previous Article | Next Article 
Journal of Virology, February 2003, p. 1885-1893, Vol. 77, No. 3
0022-538X/03/$08.00+0 DOI: 10.1128/JVI.77.3.1885-1893.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Conditional Replication of Duck Hepatitis B Virus in Hepatoma Cells
Ju-Tao Guo,1 Melissa Pryce,1 Xingtai Wang,2 M. Inmaculada Barrasa,1 Jianming Hu,2* and Christoph Seeger1*
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111,1
Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts 021182
Received 21 June 2002/
Accepted 20 October 2002
To facilitate investigations of replication and host cell interactions in the hepadnavirus system, we have developed cell lines permitting the conditional replication of duck hepatitis B virus (DHBV). With the help of this system, we devised conditions for core particle isolation that preserve replicase activity, which was not found in previous preparations. Investigations of the stability of viral DNA intermediates indicated that both encapsidated DNA and covalently closed circular DNA (cccDNA) were turned over independently of cell division. Moreover, we showed that alpha interferon reduced the accumulation of RNA-containing viral particles. The availability of a synchronized replication system will permit the biochemical analysis of individual steps of the viral replication cycle, including the mechanism and regulation of cccDNA formation.
* Corresponding authors. Mailing address for C. Seeger: Fox Chase Cancer Center, 7701 Burholme Ave., Philadelphia, PA 19111. Phone: (215) 728-4312. Fax: (215) 728-4329. E-mail:
c_seeger{at}fccc.edu. Mailing address for J. Hu: Department of Microbiology, Boston University School of Medicine, 80 E. Concord St., Boston, MA 02118. Phone: (617) 638-4982. Fax: (617) 618-4286. E-mail:
jmhu{at}bu.edu.
Journal of Virology, February 2003, p. 1885-1893, Vol. 77, No. 3
0022-538X/03/$08.00+0 DOI: 10.1128/JVI.77.3.1885-1893.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Guo, H., Jiang, D., Ma, D., Chang, J., Dougherty, A. M., Cuconati, A., Block, T. M., Guo, J.-T.
(2009). Activation of Pattern Recognition Receptor-Mediated Innate Immunity Inhibits the Replication of Hepatitis B Virus in Human Hepatocyte-Derived Cells. J. Virol.
83: 847-858
[Abstract]
[Full Text]
-
Guo, H., Jiang, D., Zhou, T., Cuconati, A., Block, T. M., Guo, J.-T.
(2007). Characterization of the Intracellular Deproteinized Relaxed Circular DNA of Hepatitis B Virus: an Intermediate of Covalently Closed Circular DNA Formation. J. Virol.
81: 12472-12484
[Abstract]
[Full Text]
-
Guo, H., Zhou, T., Jiang, D., Cuconati, A., Xiao, G.-H., Block, T. M., Guo, J.-T.
(2007). Regulation of Hepatitis B Virus Replication by the Phosphatidylinositol 3-Kinase-Akt Signal Transduction Pathway. J. Virol.
81: 10072-10080
[Abstract]
[Full Text]
-
Gao, W., Hu, J.
(2007). Formation of Hepatitis B Virus Covalently Closed Circular DNA: Removal of Genome-Linked Protein. J. Virol.
81: 6164-6174
[Abstract]
[Full Text]
-
Nguyen, D. H., Gummuluru, S., Hu, J.
(2007). Deamination-Independent Inhibition of Hepatitis B Virus Reverse Transcription by APOBEC3G. J. Virol.
81: 4465-4472
[Abstract]
[Full Text]
-
Wang, R. Y.-L., Shen, C.-N., Lin, M.-H., Tosh, D., Shih, C.
(2005). Hepatocyte-Like Cells Transdifferentiated from a Pancreatic Origin Can Support Replication of Hepatitis B Virus. J. Virol.
79: 13116-13128
[Abstract]
[Full Text]
-
Perlman, D. H., Berg, E. A., O'Connor, P. B., Costello, C. E., Hu, J.
(2005). Reverse transcription-associated dephosphorylation of hepadnavirus nucleocapsids. Proc. Natl. Acad. Sci. USA
102: 9020-9025
[Abstract]
[Full Text]
-
Wieland, S. F., Spangenberg, H. C., Thimme, R., Purcell, R. H., Chisari, F. V.
(2004). Expansion and contraction of the hepatitis B virus transcriptional template in infected chimpanzees. Proc. Natl. Acad. Sci. USA
101: 2129-2134
[Abstract]
[Full Text]
-
Summers, J., Mason, W. S.
(2004). Residual integrated viral DNA after hepadnavirus clearance by nucleoside analog therapy. Proc. Natl. Acad. Sci. USA
101: 638-640
[Abstract]
[Full Text]