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Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus

Dissertation (MSc)--University of Pretoria, 2018.

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Other Authors: Quan, Melvyn
Format: Thesis
Language:English
Published: University of Pretoria 2018
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access_status_str Open Access
author2 Quan, Melvyn
author_browse Quan, Melvyn
author_facet Quan, Melvyn
collection Thesis
dc_rights_str_mv © 2018 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, 2018.
format Thesis
id oai:repository.up.ac.za:2263/68038
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:37:45.339Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2018
publishDateRange 2018
publishDateSort 2018
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:2263/68038 Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus Quan, Melvyn nduvukabajani@yahoo.com Kabajani, Juliet Ndubu Unrestricted UCTD Dissertation (MSc)--University of Pretoria, 2018. Cevac® Transmune® IBD was developed by CEVA Santé Animale for vaccination of poultry against infectious bursal disease (IBD, or Gumboro). The vaccine contains the Winterfield 2512 (W2512) strain of infectious bursal disease virus (IBDV). There is currently no rapid method to detect this strain specifically in fowl vaccinated with the Transmune® vaccine. This study describes the development and optimisation of a real-time RT-PCR assay that is sensitive and specific for the W2512 strain in Cevac® Transmune® IBD vaccine. IBDV sequences available publically on Genbank were downloaded and aligned. No sequence unique to IBDV W2512 Segment B was identified in the downloaded sequences, so sequencing of the IBDV W2512 Segment A was undertaken. A single nucleotide polymorphism (SNP) at nucleotide position 2451 of segment A of IBDV W2512 was identified. An assay targeting this SNP was designed and made use of a TaqMan™ minor groove binding (MGB) probe. The optimum primer and probe concentrations of the assay were 200 nM and 100 nM respectively. The efficiency of the assay was 87%, with an R2 of 0.9924. The 95% limit of detection (LOD) was determined through probit analysis (SPSS) of 25 replicates of a two-fold dilution series and determined to be of 4.7x10-5 chicken infection dose (CID50) (95% confidence interval of 1.7x10-5 to 3.4x10-5). The assay was found to be potentially specific after testing other IBDV strains (IBD#6 vero, isolate 1327108, isolate IBDV). However, there is a need to investigate the specificity further by validating the assay with more IBDV field and vaccine strains. The assay was also tested on 12 W2512 positive and 12 W2512 negative impression smears of bursa samples stored on Whatman® FTA cards. All the 12-W2512 negative samples tested negative while 11 out of 12-W2512 positive samples tested positive with this assay. Based on these performance characteristics and findings, the assay is sensitive and could be specific for Cevac® Transmune® IBD’s W2512 vaccine strain. It is rapid, efficient, easy to perform and may be suitable for its intended use, which is to detect W2512 IBDV strain in poultry flock vaccinated with Cevac® Transmune® IBD vaccine. Veterinary Tropical Diseases MSc Unrestricted 2018-12-05T08:06:32Z 2018-12-05T08:06:32Z 2009/08/18 2018 Dissertation Kabajani, JN 2018, Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus, MSc Dissertation, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/68038> S2018 http://hdl.handle.net/2263/68038 en © 2018 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 Unrestricted
UCTD
Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title_full Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title_fullStr Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title_full_unstemmed Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title_short Development of a real-time RT-PCR assay specific for the Winterfield 2512 strain of infectious bursal disease virus
title_sort development of a real time rt pcr assay specific for the winterfield 2512 strain of infectious bursal disease virus
topic Unrestricted
UCTD
url http://hdl.handle.net/2263/68038