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Sequence diversity of hepatitis D virus in Mongolia

INTRODUCTION: The Hepatitis Delta Virus (HDV) is a defective, single-stranded RNA virusoid encoding for a single protein, the Hepatitis Delta Antigen (HDAg), which requires the hepatitis B virus (HBV) envelope protein (HBsAg) for its transmission. Currently, hepatitis D is the most aggressive form o...

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Autores principales: Magvan, Battur, Kloeble, Anne Alina, Ptok, Johannes, Hoffmann, Daniel, Habermann, Daniel, Gantumur, Anuujin, Paluschinski, Martha, Enebish, Gerelmaa, Balz, Vera, Fischer, Johannes C., Chimeddorj, Battogtokh, Walker, Andreas, Timm, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077969/
https://www.ncbi.nlm.nih.gov/pubmed/37035318
http://dx.doi.org/10.3389/fmed.2023.1108543
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author Magvan, Battur
Kloeble, Anne Alina
Ptok, Johannes
Hoffmann, Daniel
Habermann, Daniel
Gantumur, Anuujin
Paluschinski, Martha
Enebish, Gerelmaa
Balz, Vera
Fischer, Johannes C.
Chimeddorj, Battogtokh
Walker, Andreas
Timm, Jörg
author_facet Magvan, Battur
Kloeble, Anne Alina
Ptok, Johannes
Hoffmann, Daniel
Habermann, Daniel
Gantumur, Anuujin
Paluschinski, Martha
Enebish, Gerelmaa
Balz, Vera
Fischer, Johannes C.
Chimeddorj, Battogtokh
Walker, Andreas
Timm, Jörg
author_sort Magvan, Battur
collection PubMed
description INTRODUCTION: The Hepatitis Delta Virus (HDV) is a defective, single-stranded RNA virusoid encoding for a single protein, the Hepatitis Delta Antigen (HDAg), which requires the hepatitis B virus (HBV) envelope protein (HBsAg) for its transmission. Currently, hepatitis D is the most aggressive form of viral hepatitis and treatment options are limited. Worldwide 12 million people are chronically infected with HDV being at high risk for progression to cirrhosis and development of liver cancer. OBJECTIVES: Although it is well established that Mongolia is the country with the highest prevalence of HDV infections, the information on the molecular epidemiology and factors contributing to HDV sequence diversity are largely unclear. The aim of the study was to characterize the sequence diversity of HDV in rural areas from Mongolia and to determine the extent of HLA class I-associated selection pressure. PATIENTS AND METHODS: From the HepMongolia cohort from rural areas in Mongolia, 451 HBsAg-positive individuals were selected and anti-HDV, HDV-RNA and the sequence of the large HDAg was determined. For all individuals the HLA class I locus was genotyped. Residues under selection pressure in the presence of individual HLA class I types were identified with the recently published analysis tool HAMdetector. RESULTS: Of 431 HBsAg positive patients, 281 were anti-HDV positive (65%), and HDV-RNA could be detected in 207 of 281 (74%) of patients. The complete large HDAg was successfully sequenced from 131 samples. Phylogenetic analysis revealed that all Mongolian HDV isolates belong to genotype 1, however, they separate into several different clusters without clear regional association. In turn, from phylogeny there is strong evidence for recent local transmission events. Importantly, we found multiple residues with strong support for HLA class I-associated selection pressure consistent with a functional CD8(+) T cell response directed against HDV. CONCLUSION: HDV isolates from Mongolia are highly diverse. The molecular epidemiology suggests circulation of multiple subtypes and provides evidence for ongoing recent transmissions.
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spelling pubmed-100779692023-04-07 Sequence diversity of hepatitis D virus in Mongolia Magvan, Battur Kloeble, Anne Alina Ptok, Johannes Hoffmann, Daniel Habermann, Daniel Gantumur, Anuujin Paluschinski, Martha Enebish, Gerelmaa Balz, Vera Fischer, Johannes C. Chimeddorj, Battogtokh Walker, Andreas Timm, Jörg Front Med (Lausanne) Medicine INTRODUCTION: The Hepatitis Delta Virus (HDV) is a defective, single-stranded RNA virusoid encoding for a single protein, the Hepatitis Delta Antigen (HDAg), which requires the hepatitis B virus (HBV) envelope protein (HBsAg) for its transmission. Currently, hepatitis D is the most aggressive form of viral hepatitis and treatment options are limited. Worldwide 12 million people are chronically infected with HDV being at high risk for progression to cirrhosis and development of liver cancer. OBJECTIVES: Although it is well established that Mongolia is the country with the highest prevalence of HDV infections, the information on the molecular epidemiology and factors contributing to HDV sequence diversity are largely unclear. The aim of the study was to characterize the sequence diversity of HDV in rural areas from Mongolia and to determine the extent of HLA class I-associated selection pressure. PATIENTS AND METHODS: From the HepMongolia cohort from rural areas in Mongolia, 451 HBsAg-positive individuals were selected and anti-HDV, HDV-RNA and the sequence of the large HDAg was determined. For all individuals the HLA class I locus was genotyped. Residues under selection pressure in the presence of individual HLA class I types were identified with the recently published analysis tool HAMdetector. RESULTS: Of 431 HBsAg positive patients, 281 were anti-HDV positive (65%), and HDV-RNA could be detected in 207 of 281 (74%) of patients. The complete large HDAg was successfully sequenced from 131 samples. Phylogenetic analysis revealed that all Mongolian HDV isolates belong to genotype 1, however, they separate into several different clusters without clear regional association. In turn, from phylogeny there is strong evidence for recent local transmission events. Importantly, we found multiple residues with strong support for HLA class I-associated selection pressure consistent with a functional CD8(+) T cell response directed against HDV. CONCLUSION: HDV isolates from Mongolia are highly diverse. The molecular epidemiology suggests circulation of multiple subtypes and provides evidence for ongoing recent transmissions. Frontiers Media S.A. 2023-03-13 /pmc/articles/PMC10077969/ /pubmed/37035318 http://dx.doi.org/10.3389/fmed.2023.1108543 Text en Copyright © 2023 Magvan, Kloeble, Ptok, Hoffmann, Habermann, Gantumur, Paluschinski, Enebish, Balz, Fischer, Chimeddorj, Walker and Timm. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Magvan, Battur
Kloeble, Anne Alina
Ptok, Johannes
Hoffmann, Daniel
Habermann, Daniel
Gantumur, Anuujin
Paluschinski, Martha
Enebish, Gerelmaa
Balz, Vera
Fischer, Johannes C.
Chimeddorj, Battogtokh
Walker, Andreas
Timm, Jörg
Sequence diversity of hepatitis D virus in Mongolia
title Sequence diversity of hepatitis D virus in Mongolia
title_full Sequence diversity of hepatitis D virus in Mongolia
title_fullStr Sequence diversity of hepatitis D virus in Mongolia
title_full_unstemmed Sequence diversity of hepatitis D virus in Mongolia
title_short Sequence diversity of hepatitis D virus in Mongolia
title_sort sequence diversity of hepatitis d virus in mongolia
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077969/
https://www.ncbi.nlm.nih.gov/pubmed/37035318
http://dx.doi.org/10.3389/fmed.2023.1108543
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