HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations

Hepatitis B virus (HBV) genotypes and mutants have been associated with differences in clinical and virological characteristics. Autophagy is a cellular process that degrades long-lived proteins and damaged organelles. Viruses have evolved mechanisms to alter this process to survive in host cells. I...

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Detalles Bibliográficos
Publicado: 2018
Materias:
acidification
article
autophagosome
autophagy
Hepatitis B virus
hepatoma cell
human cell
liver cell
lysosome
modulation
mutation
nonhuman
protein degradation
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v13_n5_p_Elizalde
http://hdl.handle.net/20.500.12110/paper_19326203_v13_n5_p_Elizalde
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paper:paper_19326203_v13_n5_p_Elizalde
record_format dspace
spelling paper:paper_19326203_v13_n5_p_Elizalde2025-07-30T19:06:25Z HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations acidification article autophagosome autophagy Hepatitis B virus hepatoma cell human cell liver cell lysosome modulation mutation nonhuman protein degradation Hepatitis B virus (HBV) genotypes and mutants have been associated with differences in clinical and virological characteristics. Autophagy is a cellular process that degrades long-lived proteins and damaged organelles. Viruses have evolved mechanisms to alter this process to survive in host cells. In this work, we studied the modulation of autophagy by the replication of HBV subgenotypes F1b and F4, and the naturally occurring mutants BCP and preCore. HBV subgenotypes F1b and F4 replication induced accumulation of autophagosomes in hepatoma cells. However, no autophagic protein degradation was observed, indicating a blockage of autophagic flux at later stages. This inhibition of autophagy flux might be due to an impairment of lysosomal acidification in hepatoma cells. Moreover, HBV-mediated autophagy modulation was independent of the viral subgenotypes and enhanced in viruses with BCP and preCore naturally occurring mutations. These results contribute to understand the mechanisms by which different HBV variants contribute to the pathogenesis of HBV infections. In addition, this study is the first to describe the role that two highly prevalent naturally occurring mutations exert on the modulation of HBV-induced autophagy. © 2018 Elizalde et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 2018 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v13_n5_p_Elizalde http://hdl.handle.net/20.500.12110/paper_19326203_v13_n5_p_Elizalde
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic acidification
article
autophagosome
autophagy
Hepatitis B virus
hepatoma cell
human cell
liver cell
lysosome
modulation
mutation
nonhuman
protein degradation
spellingShingle acidification
article
autophagosome
autophagy
Hepatitis B virus
hepatoma cell
human cell
liver cell
lysosome
modulation
mutation
nonhuman
protein degradation
HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
topic_facet acidification
article
autophagosome
autophagy
Hepatitis B virus
hepatoma cell
human cell
liver cell
lysosome
modulation
mutation
nonhuman
protein degradation
description Hepatitis B virus (HBV) genotypes and mutants have been associated with differences in clinical and virological characteristics. Autophagy is a cellular process that degrades long-lived proteins and damaged organelles. Viruses have evolved mechanisms to alter this process to survive in host cells. In this work, we studied the modulation of autophagy by the replication of HBV subgenotypes F1b and F4, and the naturally occurring mutants BCP and preCore. HBV subgenotypes F1b and F4 replication induced accumulation of autophagosomes in hepatoma cells. However, no autophagic protein degradation was observed, indicating a blockage of autophagic flux at later stages. This inhibition of autophagy flux might be due to an impairment of lysosomal acidification in hepatoma cells. Moreover, HBV-mediated autophagy modulation was independent of the viral subgenotypes and enhanced in viruses with BCP and preCore naturally occurring mutations. These results contribute to understand the mechanisms by which different HBV variants contribute to the pathogenesis of HBV infections. In addition, this study is the first to describe the role that two highly prevalent naturally occurring mutations exert on the modulation of HBV-induced autophagy. © 2018 Elizalde et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
title HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
title_short HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
title_full HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
title_fullStr HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
title_full_unstemmed HBV subgenotypes F1b and F4 replication induces an incomplete autophagic process in hepatocytes: Role of BCP and preCore mutations
title_sort hbv subgenotypes f1b and f4 replication induces an incomplete autophagic process in hepatocytes: role of bcp and precore mutations
publishDate 2018
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v13_n5_p_Elizalde
http://hdl.handle.net/20.500.12110/paper_19326203_v13_n5_p_Elizalde
_version_ 1840327031737286656

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