Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C

The hepatitis G virus and GBV-C are recently discovered variants of the same virus belonging to the family Flavivirus (HGV/GBV-C). Although initially thought to be a hepatitis virus, it has been shown to have no association with liver disease. No work has been performed on the prevalence or molecula...

Full description

Saved in:
Bibliographic Details
Main Author: Tucker, Timothy Johan Paul
Other Authors: Kirsch, Ralph
Format: Thesis
Language:English
Published: Division of Virology 2017
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867614357490237440
access_status_str Open Access
author Tucker, Timothy Johan Paul
author2 Kirsch, Ralph
author_browse Kirsch, Ralph
Tucker, Timothy Johan Paul
author_facet Kirsch, Ralph
Tucker, Timothy Johan Paul
author_sort Tucker, Timothy Johan Paul
collection Thesis
description The hepatitis G virus and GBV-C are recently discovered variants of the same virus belonging to the family Flavivirus (HGV/GBV-C). Although initially thought to be a hepatitis virus, it has been shown to have no association with liver disease. No work has been performed on the prevalence or molecular characteristics of HGV/GBV-C in southern Africa. In addition, although it is clear that the liver is not the primary site of replication, there is no data on the sites of HGV/GBV-C replication in normal subjects. Thus, this study aimed to assess the prevalence of HGV/GBV-C carriage in the urban and rural adult Black communities of the Western and Eastern Cape Provinces of South Africa, and compare it to the prevalence of serological markers of the hepatitis viruses A-E. In addition, this study aimed to assess the molecular features of South African HGV/GBV-C isolates and demonstrate the organs where viral replication was present. The mean prevalences of antibodies to hepatitis A lgG, hepatitis B surface antigen and antibodies to hepatitis B surface antigen were 98%, 4.3% and 61.1 % respectively. The mean prevalence of antibodies to hepatitis C was 1.8%. No significant differences in prevalence were shown between the urban and rural regions for these viruses. The mean anti-hepatitis E prevalence varied from 5.8% to 19.1 % in the different regions. Those living in mud houses without access to chlorinated tap water had a significantly higher prevalence of antihepatitis E. No anti-hepatitis D positive samples were isolated. The overall prevalence of HGV/GBV-C was 26.9%, with rural communities having a significantly lower prevalence than urban communities. A significant relationship was observed between HGV/GBV-C infection with the use of illicit drugs, female gender, younger age and past blood transfusions. Phylogenetic analysis demonstrated a novel fourth South African HGV/GBV-C genotype, distinct from the previously described genotypes 1-3. In addition, certain isolates showed a major deletion in the highly conserved 5' non-coding region of HGV/GBV-C. Analysis of 23 tissue biopsies from infected cadavers suggested that the spleen and bone marrow were the primary sites of HGV/GBVC replication.
format Thesis
id oai:open.uct.ac.za:11427/25669
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:50:45.690Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2017
publishDateRange 2017
publishDateSort 2017
publisher Division of Virology
publisherStr Division of Virology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/25669 Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C Tucker, Timothy Johan Paul Kirsch, Ralph Robson, Simon Hepatitis C-Like Viruses Virology The hepatitis G virus and GBV-C are recently discovered variants of the same virus belonging to the family Flavivirus (HGV/GBV-C). Although initially thought to be a hepatitis virus, it has been shown to have no association with liver disease. No work has been performed on the prevalence or molecular characteristics of HGV/GBV-C in southern Africa. In addition, although it is clear that the liver is not the primary site of replication, there is no data on the sites of HGV/GBV-C replication in normal subjects. Thus, this study aimed to assess the prevalence of HGV/GBV-C carriage in the urban and rural adult Black communities of the Western and Eastern Cape Provinces of South Africa, and compare it to the prevalence of serological markers of the hepatitis viruses A-E. In addition, this study aimed to assess the molecular features of South African HGV/GBV-C isolates and demonstrate the organs where viral replication was present. The mean prevalences of antibodies to hepatitis A lgG, hepatitis B surface antigen and antibodies to hepatitis B surface antigen were 98%, 4.3% and 61.1 % respectively. The mean prevalence of antibodies to hepatitis C was 1.8%. No significant differences in prevalence were shown between the urban and rural regions for these viruses. The mean anti-hepatitis E prevalence varied from 5.8% to 19.1 % in the different regions. Those living in mud houses without access to chlorinated tap water had a significantly higher prevalence of antihepatitis E. No anti-hepatitis D positive samples were isolated. The overall prevalence of HGV/GBV-C was 26.9%, with rural communities having a significantly lower prevalence than urban communities. A significant relationship was observed between HGV/GBV-C infection with the use of illicit drugs, female gender, younger age and past blood transfusions. Phylogenetic analysis demonstrated a novel fourth South African HGV/GBV-C genotype, distinct from the previously described genotypes 1-3. In addition, certain isolates showed a major deletion in the highly conserved 5' non-coding region of HGV/GBV-C. Analysis of 23 tissue biopsies from infected cadavers suggested that the spleen and bone marrow were the primary sites of HGV/GBVC replication. 2017-10-13T13:07:40Z 2017-10-13T13:07:40Z 1999 2017-07-14T09:36:03Z Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/25669 eng application/pdf Division of Virology Faculty of Health Sciences University of Cape Town
spellingShingle Hepatitis C-Like Viruses
Virology
Tucker, Timothy Johan Paul
Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
thesis_degree_str Doctoral
title Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
title_full Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
title_fullStr Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
title_full_unstemmed Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
title_short Epidemiology, molecular characterisation and tropism of the Hepatitis G Virus / GBV-C
title_sort epidemiology molecular characterisation and tropism of the hepatitis g virus gbv c
topic Hepatitis C-Like Viruses
Virology
url http://hdl.handle.net/11427/25669
work_keys_str_mv AT tuckertimothyjohanpaul epidemiologymolecularcharacterisationandtropismofthehepatitisgvirusgbvc