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Journal of Virology, July 2006, p. 6469-6477, Vol. 80, No. 13
0022-538X/06/$08.00+0     doi:10.1128/JVI.00245-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Genetic Changes in Hepatitis Delta Virus from Acutely and Chronically Infected Woodchucks

Department of Microbiology and Immunology, Georgetown University, Washington, D.C. 20057,¹ Division of Molecular Virology and Immunology, Georgetown University Medical Center, Rockville, Maryland 20850,² Department of Clinical Sciences, New York State College of Veterinary Medicine, Cornell University, Ithaca, New York³

Received 2 February 2006/ Accepted 12 April 2006

A woodchuck-derived hepatitis delta virus (HDV) inoculum was created by transfection of a genotype I HDV cDNA clone directly into the liver of a woodchuck that was chronically infected with woodchuck hepatitis virus. All woodchucks receiving this inoculum became positive for HDV RNA in serum, and 67% became chronically infected, similar to the rate of chronic HDV infection in humans. Analysis of HDV sequences obtained at 73 weeks postinfection indicated that changes had occurred at a rate of 0.5% per year; many of these modifications were consistent with editing by host RNA adenosine deaminase. The appearance of sequence changes, which were not evenly distributed on the genome, was correlated with the course of HDV infection. A limited number of modifications occurred in the consensus sequence of the viral genome that altered the sequence of the hepatitis delta antigen (HDAg). All chronically infected animals examined exhibited these changes 73 weeks following infection, but at earlier times, only one of the HDV carriers exhibited consensus sequence substitutions. On the other hand, sequence modifications in animals that eventually recovered from HDV infection were apparent after 27 weeks. The data are consistent with a model in which HDV sequence changes are selected by host immune responses. Chronic HDV infection in woodchucks may result from a delayed and weak immune response that is limited to a small number of epitopes on HDAg.

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