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Hepatitis delta virus infects the cells of hepadnavirus‐induced hepatocellular carcinoma in woodchucks
Author(s) -
Freitas Natalia,
Salisse Jessica,
Cunha Celso,
Toshkov Ilia,
Menne Stephan,
Gudima Severin O.
Publication year - 2012
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.25663
Subject(s) - virology , hepatocellular carcinoma , hepatitis delta , virus , hepatitis b virus , delta , woodchuck hepatitis virus , biology , hepatitis virus , medicine , hepadnaviridae , cancer research , physics , astronomy
Abstract Hepatitis delta virus (HDV) is a natural subviral agent of human hepatitis B virus (HBV). HDV enhances liver damage during concomitant infection with HBV. The molecular pathogenesis of HDV infection remains poorly understood. To advance our understanding of the relationship between HDV infection and liver cancer, it was determined whether HDV could infect in vivo the cells of hepadnavirus‐induced hepatocellular carcinoma (HCC). Woodchucks ( Marmota monax ) that were chronically infected with HBV‐related woodchuck hepatitis virus (WHV) and already developed HCCs were used as an experimental model. The locations of HCCs within the livers were determined using ultrasound imaging followed by open surgery. One week after surgery the WHV carrier woodchucks were superinfected with WHV‐enveloped HDV (wHDV). Six weeks later the animals were sacrificed and HDV replication in normal liver tissues and in center masses of HCCs was evidenced by Northern analysis, real‐time polymerase chain reaction assay, and immunohistochemistry. Based on accumulation levels of HDV RNAs and numbers of infected cells, the efficiency of wHDV infection appears to be comparable in most HCCs and normal liver tissues. Conclusion : Cells of WHV‐induced HCCs are susceptible to HDV infection in vivo , and therefore express functional putative WHV receptors and support the steps of the attachment/entry governed by the hepadnavirus envelope proteins. Because others previously hypothesized that hepadnavirus‐induced HCCs are resistant to reinfection with a hepadnavirus in vivo , our data suggest that if such a resistance exists it likely occurs via a block at the post‐entry step. The demonstrated ability of HDV to infect already formed HCCs may facilitate development of novel strategies further dissecting the mechanism of liver pathogenesis associated with HDV infection. (H EPATOLOGY 2012;56:76–85)