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Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease

Chronic hepatitis B virus (HBV) infection is a global health problem that presents as a spectrum of liver disease, reflecting an interplay between the virus and the host immune system. HBV genomes exist as episomal covalently closed circular DNA (cccDNA) or chromosomal integrants. The relative contr...

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Autores principales: Magri, Andrea, Harris, James M., D’Arienzo, Valentina, Minisini, Rosalba, Jühling, Frank, Wing, Peter A. C., Rapetti, Rachele, Leutner, Monica, Testoni, Barbara, Baumert, Thomas F., Zoulim, Fabien, Balfe, Peter, Pirisi, Mario, McKeating, Jane A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146050/
https://www.ncbi.nlm.nih.gov/pubmed/35632812
http://dx.doi.org/10.3390/v14051070
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author Magri, Andrea
Harris, James M.
D’Arienzo, Valentina
Minisini, Rosalba
Jühling, Frank
Wing, Peter A. C.
Rapetti, Rachele
Leutner, Monica
Testoni, Barbara
Baumert, Thomas F.
Zoulim, Fabien
Balfe, Peter
Pirisi, Mario
McKeating, Jane A.
author_facet Magri, Andrea
Harris, James M.
D’Arienzo, Valentina
Minisini, Rosalba
Jühling, Frank
Wing, Peter A. C.
Rapetti, Rachele
Leutner, Monica
Testoni, Barbara
Baumert, Thomas F.
Zoulim, Fabien
Balfe, Peter
Pirisi, Mario
McKeating, Jane A.
author_sort Magri, Andrea
collection PubMed
description Chronic hepatitis B virus (HBV) infection is a global health problem that presents as a spectrum of liver disease, reflecting an interplay between the virus and the host immune system. HBV genomes exist as episomal covalently closed circular DNA (cccDNA) or chromosomal integrants. The relative contribution of these genomes to the viral transcriptome in chronic hepatitis B (CHB) is not well-understood. We developed a qPCR method to estimate the abundance of HBV cccDNA- and integrant-derived viral transcripts and applied this to a cohort of patients diagnosed with CHB in the HBe antigen negative phase of disease. We noted a variable pattern of HBV transcripts from both DNA templates, with preS1/S2 mRNAs predominating and a significant association between increasing age and the expression of integrant-derived mRNAs, but not with inflammatory status. In contrast, cccDNA-derived transcripts were associated with markers of liver inflammation. Analysis of the inflammatory hepatic transcriptome identified 24 genes significantly associated with cccDNA transcriptional activity. Our study uncovers an immune gene signature that associates with HBV cccDNA transcription and increases our understanding of viral persistence.
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spelling pubmed-91460502022-05-29 Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease Magri, Andrea Harris, James M. D’Arienzo, Valentina Minisini, Rosalba Jühling, Frank Wing, Peter A. C. Rapetti, Rachele Leutner, Monica Testoni, Barbara Baumert, Thomas F. Zoulim, Fabien Balfe, Peter Pirisi, Mario McKeating, Jane A. Viruses Article Chronic hepatitis B virus (HBV) infection is a global health problem that presents as a spectrum of liver disease, reflecting an interplay between the virus and the host immune system. HBV genomes exist as episomal covalently closed circular DNA (cccDNA) or chromosomal integrants. The relative contribution of these genomes to the viral transcriptome in chronic hepatitis B (CHB) is not well-understood. We developed a qPCR method to estimate the abundance of HBV cccDNA- and integrant-derived viral transcripts and applied this to a cohort of patients diagnosed with CHB in the HBe antigen negative phase of disease. We noted a variable pattern of HBV transcripts from both DNA templates, with preS1/S2 mRNAs predominating and a significant association between increasing age and the expression of integrant-derived mRNAs, but not with inflammatory status. In contrast, cccDNA-derived transcripts were associated with markers of liver inflammation. Analysis of the inflammatory hepatic transcriptome identified 24 genes significantly associated with cccDNA transcriptional activity. Our study uncovers an immune gene signature that associates with HBV cccDNA transcription and increases our understanding of viral persistence. MDPI 2022-05-17 /pmc/articles/PMC9146050/ /pubmed/35632812 http://dx.doi.org/10.3390/v14051070 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Magri, Andrea
Harris, James M.
D’Arienzo, Valentina
Minisini, Rosalba
Jühling, Frank
Wing, Peter A. C.
Rapetti, Rachele
Leutner, Monica
Testoni, Barbara
Baumert, Thomas F.
Zoulim, Fabien
Balfe, Peter
Pirisi, Mario
McKeating, Jane A.
Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title_full Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title_fullStr Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title_full_unstemmed Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title_short Inflammatory Gene Expression Associates with Hepatitis B Virus cccDNA- but Not Integrant-Derived Transcripts in HBeAg Negative Disease
title_sort inflammatory gene expression associates with hepatitis b virus cccdna- but not integrant-derived transcripts in hbeag negative disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9146050/
https://www.ncbi.nlm.nih.gov/pubmed/35632812
http://dx.doi.org/10.3390/v14051070
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