Cargando…

Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population

The natural history and treatment outcome of hepatitis B viruses (HBV) infection is largely dependent on genotype, subgenotype, and the presence or absence of virulence associated mutations. We have studied the prevalence of genotype and subgenotype as well as virulence and drug resistance associate...

Descripción completa

Detalles Bibliográficos
Autores principales: Munshi, Saif Ullah, Tran, Thanh Thi Thanh, Vo, Truc Nhu Thanh, Tabassum, Shahina, Sultana, Nahida, Nguyen, Trang Hoa, Jahan, Munira, Le, Chau Ngoc, Baker, Stephen, Rahman, Motiur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720799/
https://www.ncbi.nlm.nih.gov/pubmed/29216251
http://dx.doi.org/10.1371/journal.pone.0188944
_version_ 1783284733922246656
author Munshi, Saif Ullah
Tran, Thanh Thi Thanh
Vo, Truc Nhu Thanh
Tabassum, Shahina
Sultana, Nahida
Nguyen, Trang Hoa
Jahan, Munira
Le, Chau Ngoc
Baker, Stephen
Rahman, Motiur
author_facet Munshi, Saif Ullah
Tran, Thanh Thi Thanh
Vo, Truc Nhu Thanh
Tabassum, Shahina
Sultana, Nahida
Nguyen, Trang Hoa
Jahan, Munira
Le, Chau Ngoc
Baker, Stephen
Rahman, Motiur
author_sort Munshi, Saif Ullah
collection PubMed
description The natural history and treatment outcome of hepatitis B viruses (HBV) infection is largely dependent on genotype, subgenotype, and the presence or absence of virulence associated mutations. We have studied the prevalence of genotype and subgenotype as well as virulence and drug resistance associated mutations and prevalence of recombinant among HBV from Bangladesh. A prospective cross-sectional study was conducted among treatment naïve chronic HBV patients attending at Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh for HBV viral load assessment between June and August 2015. Systematical selected 50% of HBV DNA positive patients (every second patient) were enrolled. Biochemical and serological markers for HBV infection and whole genome sequencing (WGS) was performed on virus positive sample. Genotype, subgenotype, virulence, nucleos(t)ide analogue (NA) resistance (NAr) mutations, and the prevalence of recombinant isolates were determined. Among 114 HBV DNA positive patients, 57 were enrolled in the study and 53 HBV WGS were generated for downstream analysis. Overall, 38% (22/57) and 62% (35/57) of patients had acute and chronic HBV infections, respectively. The prevalence of genotypes A, C, and D was 18.9% (10/53), 45.3% (24/53), and 35.8% (19/53), respectively. Among genotype A, C and D isolates subgenotype A1 (90%; 9/10), C1 (87.5%; 21/24) and D2 (78.9%; 15/19) predominates. The acute infection, virulence associated mutations, and viral load was higher in the genotype D isolates. Evidence of recombination was identified in 22.6% (12/53) of the HBV isolates including 20.0% (2/10), and 16.7% (4/24) and 31.6% (6/19) of genotype A, C and D isolates, respectively. The prevalence of recombination was higher in chronic HVB patients (32.2%; 10/31 versus 9.1%; 2/22); p<0.05. NAr mutations were identified in 47.2% (25/53) of the isolates including 33.9% novel mutations (18/53). HBV genotype C and D predominated in this population in Bangladesh; a comparatively high prevalence of recombinant HBV are circulating in this setting.
format Online
Article
Text
id pubmed-5720799
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-57207992017-12-15 Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population Munshi, Saif Ullah Tran, Thanh Thi Thanh Vo, Truc Nhu Thanh Tabassum, Shahina Sultana, Nahida Nguyen, Trang Hoa Jahan, Munira Le, Chau Ngoc Baker, Stephen Rahman, Motiur PLoS One Research Article The natural history and treatment outcome of hepatitis B viruses (HBV) infection is largely dependent on genotype, subgenotype, and the presence or absence of virulence associated mutations. We have studied the prevalence of genotype and subgenotype as well as virulence and drug resistance associated mutations and prevalence of recombinant among HBV from Bangladesh. A prospective cross-sectional study was conducted among treatment naïve chronic HBV patients attending at Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh for HBV viral load assessment between June and August 2015. Systematical selected 50% of HBV DNA positive patients (every second patient) were enrolled. Biochemical and serological markers for HBV infection and whole genome sequencing (WGS) was performed on virus positive sample. Genotype, subgenotype, virulence, nucleos(t)ide analogue (NA) resistance (NAr) mutations, and the prevalence of recombinant isolates were determined. Among 114 HBV DNA positive patients, 57 were enrolled in the study and 53 HBV WGS were generated for downstream analysis. Overall, 38% (22/57) and 62% (35/57) of patients had acute and chronic HBV infections, respectively. The prevalence of genotypes A, C, and D was 18.9% (10/53), 45.3% (24/53), and 35.8% (19/53), respectively. Among genotype A, C and D isolates subgenotype A1 (90%; 9/10), C1 (87.5%; 21/24) and D2 (78.9%; 15/19) predominates. The acute infection, virulence associated mutations, and viral load was higher in the genotype D isolates. Evidence of recombination was identified in 22.6% (12/53) of the HBV isolates including 20.0% (2/10), and 16.7% (4/24) and 31.6% (6/19) of genotype A, C and D isolates, respectively. The prevalence of recombination was higher in chronic HVB patients (32.2%; 10/31 versus 9.1%; 2/22); p<0.05. NAr mutations were identified in 47.2% (25/53) of the isolates including 33.9% novel mutations (18/53). HBV genotype C and D predominated in this population in Bangladesh; a comparatively high prevalence of recombinant HBV are circulating in this setting. Public Library of Science 2017-12-07 /pmc/articles/PMC5720799/ /pubmed/29216251 http://dx.doi.org/10.1371/journal.pone.0188944 Text en © 2017 Munshi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Munshi, Saif Ullah
Tran, Thanh Thi Thanh
Vo, Truc Nhu Thanh
Tabassum, Shahina
Sultana, Nahida
Nguyen, Trang Hoa
Jahan, Munira
Le, Chau Ngoc
Baker, Stephen
Rahman, Motiur
Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title_full Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title_fullStr Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title_full_unstemmed Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title_short Molecular characterization of hepatitis B virus in Bangladesh reveals a highly recombinant population
title_sort molecular characterization of hepatitis b virus in bangladesh reveals a highly recombinant population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720799/
https://www.ncbi.nlm.nih.gov/pubmed/29216251
http://dx.doi.org/10.1371/journal.pone.0188944
work_keys_str_mv AT munshisaifullah molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT tranthanhthithanh molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT votrucnhuthanh molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT tabassumshahina molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT sultananahida molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT nguyentranghoa molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT jahanmunira molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT lechaungoc molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT bakerstephen molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation
AT rahmanmotiur molecularcharacterizationofhepatitisbvirusinbangladeshrevealsahighlyrecombinantpopulation