Animal Models and the Molecular Biology of Hepadnavirus Infection

Abstract

Australian antigen, the envelope protein of hepatitis B virus (HBV), was discovered in 1967 as a prevalent serum antigen in hepatitis B patients. Early electron microscopy (EM) studies showed that this antigen was present in 22-nm particles in patient sera, which were believed to be incomplete virus. Complete virus, much less abundant than the 22-nm particles, was finally visualized in 1970. HBV was soon found to infect chimpanzees, gorillas, orangutans, gibbon apes, and, more recently, tree shrews (Tupaia belangeri) and cynomolgus macaques (Macaca fascicularis). This restricted host range placed limits on the kinds of studies that might be performed to better understand the biology and molecular biology of HBV and to develop antiviral therapies to treat chronic infections. About 10 years after the discovery of HBV, this problem was bypassed with the discovery of viruses related to HBV in woodchucks, ground squirrels, and ducks. Although unlikely animal models, their use revealed the key steps in hepadnavirus replication and in the host response to infection, including the fact that the viral nuclear episome is the ultimate target for immune clearance of transient infections and antiviral therapy of chronic infections. Studies with these and other animal models have also suggested interesting clues into the link between chronic HBV infection and hepatocellular carcinoma.

Experimental models of hepatitis B and C — new insights and progress

“…We recommend more targeted references for precise virological and model-specific information. For hepatitis B, we recommend published papers specifically in the areas of in vitro culture systems and virology 8,9 , animal models 10,11 and those that address these topics more broadly 12,13 . Similarly, for hepatitis C, we recommend published papers specifically in the areas of in vitro culture systems and virology 14,15 , animal models 16,17 and those that address these topics more broadly 18,19 .…”

Sodium taurocholate cotransporting polypeptide is the limiting host factor of hepatitis B virus infection in macaque and pig hepatocytes

“…HBV shows a peculiar host range, infecting only humans, chimpanzees, and, under certain experimental conditions, the tree shrew Tupaia belangeri. (7) Laboratory animals such as mice, rats, and macaques are resistant to HBV and HDV infection. (8) The chimpanzee, therefore, remains the only immunocompetent model for HBV and HDV.…”

Different obesity phenotypes correlated with the PI3K-AKT signaling pathway in tree shrews

“…Based on the criteria of both MTRs＞0.5 and their gene intra-modular connectivity mentioned previously, we selected 3 modules for further annotation: the blue module (481 genes), the brown module (389 genes) and the turquoise module (1781 genes). 10 We found enriched GO terms and KEGG pathways in the 3 modules. P-values were adjusted using the Benjamini-Hochberg (BH) correction.…”