Cargando…

A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype

It was recently suggested that the composition of circulating hepatitis B subviral particles (SVPs) could be used to differentiate the various stages in chronic hepatitis B virus (HBV) infection, with significantly lower proportions of L and M proteins in inactive carriers than in individuals with c...

Descripción completa

Detalles Bibliográficos
Autores principales: Eymieux, Sébastien, Hourioux, Christophe, Marlet, Julien, Moreau, Alain, Patient, Romuald, d'Alteroche, Louis, Gaudy‐Graffin, Catherine, Blanchard, Emmanuelle, Roingeard, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541738/
https://www.ncbi.nlm.nih.gov/pubmed/35633087
http://dx.doi.org/10.1111/jvh.13712
_version_ 1784803990756655104
author Eymieux, Sébastien
Hourioux, Christophe
Marlet, Julien
Moreau, Alain
Patient, Romuald
d'Alteroche, Louis
Gaudy‐Graffin, Catherine
Blanchard, Emmanuelle
Roingeard, Philippe
author_facet Eymieux, Sébastien
Hourioux, Christophe
Marlet, Julien
Moreau, Alain
Patient, Romuald
d'Alteroche, Louis
Gaudy‐Graffin, Catherine
Blanchard, Emmanuelle
Roingeard, Philippe
author_sort Eymieux, Sébastien
collection PubMed
description It was recently suggested that the composition of circulating hepatitis B subviral particles (SVPs) could be used to differentiate the various stages in chronic hepatitis B virus (HBV) infection, with significantly lower proportions of L and M proteins in inactive carriers than in individuals with chronic hepatitis. L protein is abundant in virions and filamentous SVPs but almost absent from spherical SVPs. We, therefore, performed a morphometric analysis of SVPs in these two groups of patients, by conducting a retrospective analysis on sera from 15 inactive carriers and 11 patients with chronic hepatitis infected with various HBV genotypes. Subviral particles were concentrated by centrifugation on a sucrose cushion, with monitoring by transmission electron microscopy. The percentage of filamentous SVPs and filament length for 100 SVPs was determined with a digital camera. The L protein PreS1 promoter was sequenced from viral genomes by the Sanger method. No marked differences were found between patients, some of whom had only spherical SVPs, whereas others had variable percentages of filamentous SVPs (up to 28%), of highly variable length. High filament percentages were not associated with a particular sequence of the L protein promoter, HBV genotype or even disease stage. High levels of circulating filamentous SVPs are probably more strongly related to individual host factors than to viral strain characteristics or disease stage.
format Online
Article
Text
id pubmed-9541738
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-95417382022-10-14 A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype Eymieux, Sébastien Hourioux, Christophe Marlet, Julien Moreau, Alain Patient, Romuald d'Alteroche, Louis Gaudy‐Graffin, Catherine Blanchard, Emmanuelle Roingeard, Philippe J Viral Hepat Original Articles It was recently suggested that the composition of circulating hepatitis B subviral particles (SVPs) could be used to differentiate the various stages in chronic hepatitis B virus (HBV) infection, with significantly lower proportions of L and M proteins in inactive carriers than in individuals with chronic hepatitis. L protein is abundant in virions and filamentous SVPs but almost absent from spherical SVPs. We, therefore, performed a morphometric analysis of SVPs in these two groups of patients, by conducting a retrospective analysis on sera from 15 inactive carriers and 11 patients with chronic hepatitis infected with various HBV genotypes. Subviral particles were concentrated by centrifugation on a sucrose cushion, with monitoring by transmission electron microscopy. The percentage of filamentous SVPs and filament length for 100 SVPs was determined with a digital camera. The L protein PreS1 promoter was sequenced from viral genomes by the Sanger method. No marked differences were found between patients, some of whom had only spherical SVPs, whereas others had variable percentages of filamentous SVPs (up to 28%), of highly variable length. High filament percentages were not associated with a particular sequence of the L protein promoter, HBV genotype or even disease stage. High levels of circulating filamentous SVPs are probably more strongly related to individual host factors than to viral strain characteristics or disease stage. John Wiley and Sons Inc. 2022-06-07 2022-09 /pmc/articles/PMC9541738/ /pubmed/35633087 http://dx.doi.org/10.1111/jvh.13712 Text en © 2022 The Authors. Journal of Viral Hepatitis published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Eymieux, Sébastien
Hourioux, Christophe
Marlet, Julien
Moreau, Alain
Patient, Romuald
d'Alteroche, Louis
Gaudy‐Graffin, Catherine
Blanchard, Emmanuelle
Roingeard, Philippe
A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title_full A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title_fullStr A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title_full_unstemmed A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title_short A morphometric analysis of hepatitis B subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
title_sort morphometric analysis of hepatitis b subviral particles shows no correlation of filament proportion and length with clinical stage and genotype
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541738/
https://www.ncbi.nlm.nih.gov/pubmed/35633087
http://dx.doi.org/10.1111/jvh.13712
work_keys_str_mv AT eymieuxsebastien amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT houriouxchristophe amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT marletjulien amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT moreaualain amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT patientromuald amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT dalterochelouis amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT gaudygraffincatherine amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT blanchardemmanuelle amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT roingeardphilippe amorphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT eymieuxsebastien morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT houriouxchristophe morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT marletjulien morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT moreaualain morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT patientromuald morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT dalterochelouis morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT gaudygraffincatherine morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT blanchardemmanuelle morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype
AT roingeardphilippe morphometricanalysisofhepatitisbsubviralparticlesshowsnocorrelationoffilamentproportionandlengthwithclinicalstageandgenotype