Full Text Available

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

Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses

Dissertation (MSc)--University of Pretoria, 2015.

Saved in:
Bibliographic Details
Other Authors: Fehrsen, Jeanni
Format: Thesis
Language:English
Published: University of Pretoria 2016
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613439505989632
access_status_str Open Access
author2 Fehrsen, Jeanni
author_browse Fehrsen, Jeanni
author_facet Fehrsen, Jeanni
collection Thesis
dc_rights_str_mv © 2016 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc)--University of Pretoria, 2015.
format Thesis
id oai:repository.up.ac.za:2263/53303
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:36:10.076Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/53303 Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses Fehrsen, Jeanni mathebulaem@arc.agric.za Pretorius, Alri Mathebula, Evans Mantiri UCTD Dissertation (MSc)--University of Pretoria, 2015. African horse sickness is an infectious, insect-borne but non-contagious disease of equids responsible for more than 95% mortality in naïve horses. The African horse sickness virus has ten segments of double stranded RNA encoding seven structural and three non-structural proteins. There is currently no cure for the disease and one of the effective ways to control or prevent new infection is by vaccination. Although successful, the currently used vaccine is not registered for use outside the sub- Saharan region because of fears of reversal to virulence. Inactivated and subunit vaccines have been tested but are not commercially available. Research towards recombinant vaccines that will offer protection without these limitations is thus ongoing. Identification and characterisation of antigenic regions on proteins has always been essential in the development of vaccines and immunodiagnostic reagents. AHSV proteins have been shown to confer protection to model animals in one form or another. This study was undertaken to investigate the global humoral immune reaction during immunisation in horses. This was done using sera from immunised horses and a genome-targeted phage display library. A phage library expressing a repertoire of AHSV-4 peptides large enough to represent the whole genome was constructed. The library was affinity selected with purified naïve (day 0) and immunised (day 28, day 52) horse IgGs and a pool of phages expressing binding peptides were isolated. The DNA inserts of the pool of phages were subjected to high throughput sequencing and sequences identified by matching them to the AHSV-4 genome. Analysis of the extensive data output selected by the naive and immunised IgGs enabled a thorough examination of the panning process. Sequences were normalised by subtracting the naïve from the immunised sequences. Comparing the sequences selected with day 28 IgG enabled identification of 16 potentially antigenic regions recognised by most horses. Some of these regions could easily have been missed with the traditional clone picking approach. Some of the regions were also selected by most horses with day 52 IgG, indicating persistent antibodies. Potentially antigenic regions were identified without the functional re-testing which is common part of traditional phage display. This was due to lack of access to the single clones in the library. One way to confirm binding of selected regions is by peptide ELISA, which was started in this study. This study improved on all the phage display work already done on orbiviruses and offered more information on the immunogenicity of AHSV-4 in horses. Future work should focus on confirming antigenicity of the selected regions. The potential antigenic regions could be fused with T-cell epitopes, identified in a parallel study, to form a construct that might induce production of humoral and cellular immune responses. tm2016 Veterinary Tropical Diseases MSc 2016-06-22T08:00:41Z 2016-06-22T08:00:41Z 2016-04-21 2015 Dissertation Mathebula, EM 2015, Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses, MSc Dissertation, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/53303> A2016 http://hdl.handle.net/2263/53303 en © 2016 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle UCTD
Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title_full Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title_fullStr Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title_full_unstemmed Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title_short Identifying B-cell epitopes of African horse sickness virus serotype 4 recognised by antisera of immunised horses
title_sort identifying b cell epitopes of african horse sickness virus serotype 4 recognised by antisera of immunised horses
topic UCTD
url http://hdl.handle.net/2263/53303