Cargando…

In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations

Hepatitis B virus (HBV) infects the liver resulting in end stage liver disease, cirrhosis, and hepatocellular carcinoma. Despite an effective vaccine, HBV poses a serious health problem globally, accounting for 257 million chronic carriers. Unique features of HBV, including its narrow virus–host ran...

Descripción completa

Detalles Bibliográficos
Autores principales: Wose Kinge, Constance N., Bhoola, Nimisha H., Kramvis, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150782/
https://www.ncbi.nlm.nih.gov/pubmed/32210021
http://dx.doi.org/10.3390/v12030353
_version_ 1783521096951136256
author Wose Kinge, Constance N.
Bhoola, Nimisha H.
Kramvis, Anna
author_facet Wose Kinge, Constance N.
Bhoola, Nimisha H.
Kramvis, Anna
author_sort Wose Kinge, Constance N.
collection PubMed
description Hepatitis B virus (HBV) infects the liver resulting in end stage liver disease, cirrhosis, and hepatocellular carcinoma. Despite an effective vaccine, HBV poses a serious health problem globally, accounting for 257 million chronic carriers. Unique features of HBV, including its narrow virus–host range and its hepatocyte tropism, have led to major challenges in the development of suitable in vivo and in vitro model systems to recapitulate the HBV replication cycle and to test various antiviral strategies. Moreover, HBV is classified into at least nine genotypes and 35 sub-genotypes with distinct geographical distributions and prevalence, which have different natural histories of infection, clinical manifestation, and response to current antiviral agents. Here, we review various in vitro systems used to study the molecular biology of the different (sub)genotypes of HBV and their response to antiviral agents, and we discuss their strengths and limitations. Despite the advances made, no system is ideal for pan-genotypic HBV research or drug development and therefore further improvement is required. It is necessary to establish a centralized repository of HBV-related generated materials, which are readily accessible to HBV researchers, with international collaboration toward advancement and development of in vitro model systems for testing new HBV antivirals to ensure their pan-genotypic and/or customized activity.
format Online
Article
Text
id pubmed-7150782
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-71507822020-04-20 In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations Wose Kinge, Constance N. Bhoola, Nimisha H. Kramvis, Anna Viruses Review Hepatitis B virus (HBV) infects the liver resulting in end stage liver disease, cirrhosis, and hepatocellular carcinoma. Despite an effective vaccine, HBV poses a serious health problem globally, accounting for 257 million chronic carriers. Unique features of HBV, including its narrow virus–host range and its hepatocyte tropism, have led to major challenges in the development of suitable in vivo and in vitro model systems to recapitulate the HBV replication cycle and to test various antiviral strategies. Moreover, HBV is classified into at least nine genotypes and 35 sub-genotypes with distinct geographical distributions and prevalence, which have different natural histories of infection, clinical manifestation, and response to current antiviral agents. Here, we review various in vitro systems used to study the molecular biology of the different (sub)genotypes of HBV and their response to antiviral agents, and we discuss their strengths and limitations. Despite the advances made, no system is ideal for pan-genotypic HBV research or drug development and therefore further improvement is required. It is necessary to establish a centralized repository of HBV-related generated materials, which are readily accessible to HBV researchers, with international collaboration toward advancement and development of in vitro model systems for testing new HBV antivirals to ensure their pan-genotypic and/or customized activity. MDPI 2020-03-23 /pmc/articles/PMC7150782/ /pubmed/32210021 http://dx.doi.org/10.3390/v12030353 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wose Kinge, Constance N.
Bhoola, Nimisha H.
Kramvis, Anna
In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title_full In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title_fullStr In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title_full_unstemmed In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title_short In Vitro Systems for Studying Different Genotypes/Sub-Genotypes of Hepatitis B Virus: Strengths and Limitations
title_sort in vitro systems for studying different genotypes/sub-genotypes of hepatitis b virus: strengths and limitations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150782/
https://www.ncbi.nlm.nih.gov/pubmed/32210021
http://dx.doi.org/10.3390/v12030353
work_keys_str_mv AT wosekingeconstancen invitrosystemsforstudyingdifferentgenotypessubgenotypesofhepatitisbvirusstrengthsandlimitations
AT bhoolanimishah invitrosystemsforstudyingdifferentgenotypessubgenotypesofhepatitisbvirusstrengthsandlimitations
AT kramvisanna invitrosystemsforstudyingdifferentgenotypessubgenotypesofhepatitisbvirusstrengthsandlimitations