Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence
Hepatitis B Virus (HBV) is a globally-distributed pathogen and is a major cause of liver disease. HBV (or closely-related animal hepadnaviruses) can integrate into the host genome, but (unlike retroviruses) this integrated form is replication-defective. The specific role(s) of the integrated HBV DNA...
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doaj-c10cc7f3255743ffa41b634d978918c32021-01-27T00:00:48ZengMDPI AGViruses1999-49152021-01-011318018010.3390/v13020180Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and PersistenceThomas Tu0Henrik Zhang1Stephan Urban2Storr Liver Centre, Faculty of Medicine and Health, Westmead Clinical School and Westmead Institute for Medical Research, The University of Sydney, Westmead, NSW 2145, AustraliaStorr Liver Centre, Faculty of Medicine and Health, Westmead Clinical School and Westmead Institute for Medical Research, The University of Sydney, Westmead, NSW 2145, AustraliaDepartment of Infectious Diseases, Molecular Virology, Heidelberg University Hospital, Im Neuenheimer Feld 345, 69120 Heidelberg, GermanyHepatitis B Virus (HBV) is a globally-distributed pathogen and is a major cause of liver disease. HBV (or closely-related animal hepadnaviruses) can integrate into the host genome, but (unlike retroviruses) this integrated form is replication-defective. The specific role(s) of the integrated HBV DNA has been a long-standing topic of debate. Novel in vitro models of HBV infection combined with sensitive molecular assays now enable researchers to investigate this under-characterised phenomenon with greater ease and precision. This review covers the contributions these systems have made to understanding how HBV DNA integration induces liver cancer and facilitates viral persistence. We summarise the current findings into a working model of chronic HBV infection and discuss the clinical implications of this hypothetical framework on the upcoming therapeutic strategies used to curb HBV-associated pathogenesis.https://www.mdpi.com/1999-4915/13/2/180hepatitis B virusHBV DNA integrationhepatocellular carcinoma (HCC)non-homologous end joiningmicrohomology-mediated end joiningHBV double-stranded linear DNA |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas Tu Henrik Zhang Stephan Urban |
spellingShingle |
Thomas Tu Henrik Zhang Stephan Urban Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence Viruses hepatitis B virus HBV DNA integration hepatocellular carcinoma (HCC) non-homologous end joining microhomology-mediated end joining HBV double-stranded linear DNA |
author_facet |
Thomas Tu Henrik Zhang Stephan Urban |
author_sort |
Thomas Tu |
title |
Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence |
title_short |
Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence |
title_full |
Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence |
title_fullStr |
Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence |
title_full_unstemmed |
Hepatitis B Virus DNA Integration: In Vitro Models for Investigating Viral Pathogenesis and Persistence |
title_sort |
hepatitis b virus dna integration: in vitro models for investigating viral pathogenesis and persistence |
publisher |
MDPI AG |
series |
Viruses |
issn |
1999-4915 |
publishDate |
2021-01-01 |
description |
Hepatitis B Virus (HBV) is a globally-distributed pathogen and is a major cause of liver disease. HBV (or closely-related animal hepadnaviruses) can integrate into the host genome, but (unlike retroviruses) this integrated form is replication-defective. The specific role(s) of the integrated HBV DNA has been a long-standing topic of debate. Novel in vitro models of HBV infection combined with sensitive molecular assays now enable researchers to investigate this under-characterised phenomenon with greater ease and precision. This review covers the contributions these systems have made to understanding how HBV DNA integration induces liver cancer and facilitates viral persistence. We summarise the current findings into a working model of chronic HBV infection and discuss the clinical implications of this hypothetical framework on the upcoming therapeutic strategies used to curb HBV-associated pathogenesis. |
topic |
hepatitis B virus HBV DNA integration hepatocellular carcinoma (HCC) non-homologous end joining microhomology-mediated end joining HBV double-stranded linear DNA |
url |
https://www.mdpi.com/1999-4915/13/2/180 |
work_keys_str_mv |
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