Cargando…
A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh
BACKGROUND: Hepatitis E virus (HEV) infection is endemic in Bangladesh and there are occasional outbreaks. The molecular characteristics and pathogenesis of endemic and outbreak HEV strains are poorly understood. We compared the genetic relatedness and virulence associated mutations of endemic HEV s...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297744/ https://www.ncbi.nlm.nih.gov/pubmed/34293039 http://dx.doi.org/10.1371/journal.pone.0255054 |
_version_ | 1783725915273953280 |
---|---|
author | Hoa, Trang Nguyen Munshi, Saif Ullah Ngoc, Khanh Nguyen Ngoc, Chau Le Thanh, Thanh Tran Thi Akther, Tahmina Tabassum, Shahina Parvin, Nilufa Baker, Stephen Rahman, Motiur |
author_facet | Hoa, Trang Nguyen Munshi, Saif Ullah Ngoc, Khanh Nguyen Ngoc, Chau Le Thanh, Thanh Tran Thi Akther, Tahmina Tabassum, Shahina Parvin, Nilufa Baker, Stephen Rahman, Motiur |
author_sort | Hoa, Trang Nguyen |
collection | PubMed |
description | BACKGROUND: Hepatitis E virus (HEV) infection is endemic in Bangladesh and there are occasional outbreaks. The molecular characteristics and pathogenesis of endemic and outbreak HEV strains are poorly understood. We compared the genetic relatedness and virulence associated mutations of endemic HEV strains with outbreak strains. METHODS: We analyzed systematically collected serum samples from HEV immunoglobulin M (IgM) positive patients attended at Bangabandhu Sheikh Mujib Medical University, Dhaka from August 2013 to June 2015. HEV RNA positive samples were subjected to whole genome sequencing. Genotype and subtype of the strains were determined by phylogenetic analysis. Virulence associated mutations e.g. acute viral hepatitis (AVH), fulminant hepatic failure (FHF), chronic hepatitis, ribavirin treatment failure (RTF), B and T cell neutralization epitopes were determined. RESULTS: 92 HEV immunoglobulin M (IgM) antibody positive plasma samples (43 in 2013–2014 and 49 in 2014–2015) were studied. 77.1% (70/92) of the samples were HEV RNA positive. A 279 bp open reading frame (ORF) 2 and ORF 3 sequence was obtained from 54.2% (38/70) of the strains. Of these 38 strains, whole genome sequence (WGS) was obtained from 21 strains. In phylogenetic analysis of 38 (279 bp) sequence all HEV sequences belonged to genotype 1 and subtype 1a. Further phylogenetic analysis of 21 HEV WGS, Bangladeshi HEV sequences clustered with genotype 1a sequences from neighboring countries. Within genotype 1a cluster, Bangladesh HEV strains formed a separate cluster with the 2010 HEV outbreak strains from northern Bangladesh. 80.9 to 100% of the strains had A317T, T735I, L1120I, L1110F, P259S, V1479I, G1634K mutations associates AVH, FHF and RTF. Mutations in T cell recognition epitope T3, T5, T7 was observed in 76.1%, 100% and 100% of the strains respectively. CONCLUSION: Strains of HEV genotype 1a are dominant in Bangladesh and are associated with endemic and outbreak of HEV infection. HEV isolates in Bangladesh have high prevalence of virulence associated mutations and mutation which alters antigenicity to B and T cell epitopes. |
format | Online Article Text |
id | pubmed-8297744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82977442021-07-31 A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh Hoa, Trang Nguyen Munshi, Saif Ullah Ngoc, Khanh Nguyen Ngoc, Chau Le Thanh, Thanh Tran Thi Akther, Tahmina Tabassum, Shahina Parvin, Nilufa Baker, Stephen Rahman, Motiur PLoS One Research Article BACKGROUND: Hepatitis E virus (HEV) infection is endemic in Bangladesh and there are occasional outbreaks. The molecular characteristics and pathogenesis of endemic and outbreak HEV strains are poorly understood. We compared the genetic relatedness and virulence associated mutations of endemic HEV strains with outbreak strains. METHODS: We analyzed systematically collected serum samples from HEV immunoglobulin M (IgM) positive patients attended at Bangabandhu Sheikh Mujib Medical University, Dhaka from August 2013 to June 2015. HEV RNA positive samples were subjected to whole genome sequencing. Genotype and subtype of the strains were determined by phylogenetic analysis. Virulence associated mutations e.g. acute viral hepatitis (AVH), fulminant hepatic failure (FHF), chronic hepatitis, ribavirin treatment failure (RTF), B and T cell neutralization epitopes were determined. RESULTS: 92 HEV immunoglobulin M (IgM) antibody positive plasma samples (43 in 2013–2014 and 49 in 2014–2015) were studied. 77.1% (70/92) of the samples were HEV RNA positive. A 279 bp open reading frame (ORF) 2 and ORF 3 sequence was obtained from 54.2% (38/70) of the strains. Of these 38 strains, whole genome sequence (WGS) was obtained from 21 strains. In phylogenetic analysis of 38 (279 bp) sequence all HEV sequences belonged to genotype 1 and subtype 1a. Further phylogenetic analysis of 21 HEV WGS, Bangladeshi HEV sequences clustered with genotype 1a sequences from neighboring countries. Within genotype 1a cluster, Bangladesh HEV strains formed a separate cluster with the 2010 HEV outbreak strains from northern Bangladesh. 80.9 to 100% of the strains had A317T, T735I, L1120I, L1110F, P259S, V1479I, G1634K mutations associates AVH, FHF and RTF. Mutations in T cell recognition epitope T3, T5, T7 was observed in 76.1%, 100% and 100% of the strains respectively. CONCLUSION: Strains of HEV genotype 1a are dominant in Bangladesh and are associated with endemic and outbreak of HEV infection. HEV isolates in Bangladesh have high prevalence of virulence associated mutations and mutation which alters antigenicity to B and T cell epitopes. Public Library of Science 2021-07-22 /pmc/articles/PMC8297744/ /pubmed/34293039 http://dx.doi.org/10.1371/journal.pone.0255054 Text en © 2021 Hoa et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Hoa, Trang Nguyen Munshi, Saif Ullah Ngoc, Khanh Nguyen Ngoc, Chau Le Thanh, Thanh Tran Thi Akther, Tahmina Tabassum, Shahina Parvin, Nilufa Baker, Stephen Rahman, Motiur A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title | A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title_full | A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title_fullStr | A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title_full_unstemmed | A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title_short | A tightly clustered hepatitis E virus genotype 1a is associated with endemic and outbreak infections in Bangladesh |
title_sort | tightly clustered hepatitis e virus genotype 1a is associated with endemic and outbreak infections in bangladesh |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297744/ https://www.ncbi.nlm.nih.gov/pubmed/34293039 http://dx.doi.org/10.1371/journal.pone.0255054 |
work_keys_str_mv | AT hoatrangnguyen atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT munshisaifullah atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT ngockhanhnguyen atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT ngocchaule atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT thanhthanhtranthi atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT akthertahmina atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT tabassumshahina atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT parvinnilufa atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT bakerstephen atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT rahmanmotiur atightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT hoatrangnguyen tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT munshisaifullah tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT ngockhanhnguyen tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT ngocchaule tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT thanhthanhtranthi tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT akthertahmina tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT tabassumshahina tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT parvinnilufa tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT bakerstephen tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh AT rahmanmotiur tightlyclusteredhepatitisevirusgenotype1aisassociatedwithendemicandoutbreakinfectionsinbangladesh |