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Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus

Dissertation (MSc)--University of Pretoria, 2010.

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Other Authors: Weyer, Jacqueline
Format: Thesis
Published: University of Pretoria 2013
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access_status_str Open Access
author2 Weyer, Jacqueline
author_browse Weyer, Jacqueline
author_facet Weyer, Jacqueline
collection Thesis
dc_rights_str_mv © 2010, 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, 2010.
format Thesis
id oai:repository.up.ac.za:2263/28948
institution University of Pretoria (South Africa)
last_indexed 2026-06-10T12:36:41.285Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2013
publishDateRange 2013
publishDateSort 2013
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:2263/28948 Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus Weyer, Jacqueline Nel, Louis Hendrik Paweska, Janusz Tadeusz s89800232@up.ac.za Le Roux, C.A. (Chantel Anne) Rift Valley fever (RVF) Viral haemorrhagic fevers (VHFs) Rift Valley fever virus (RVFV) UCTD Dissertation (MSc)--University of Pretoria, 2010. Rift Valley fever (RVF) belongs to the group of viral haemorrhagic fevers (VHFs), most of which are zoonotic diseases causing outbreaks in animals and humans all over Africa. In the absence of haemorrhagic or specific organ manifestations, these diseases are clinically difficult to diagnose. Rapid laboratory confirmation of cases is therefore essential for timely execution of supportive treatment, appropriate case management, infection control, and tracing of contacts. Rift Valley fever virus (RVFV), a mosquito-borne pathogen, is responsible for high mortality rates and abortion in domestic ruminants, resulting in significant socio-economic losses. Furthermore, the virus is potentially infectious by aerosol, can replicate in a wide range of mosquito species and poses a bioweapon threat. The recent spread of the virus outside of the African continent, demonstrates its ability to move northwards to RVF free regions, e.g. to Europe and Northern America. Such fears fuel the international demand for reliable and validated diagnostic tools for rapid diagnosis of RVF. The aim of this study was to develop a rapid and accurate molecular tool for the detection of RVFV. A real-time loop-mediated isothermal amplification assay (LAMP) targeting the L segment of RVFV, was developed and evaluated. The assay proved to be highly specific and able to detect RVFV strains representing the genetic spectrum of the virus. Furthermore, the assay did not amplify the RNA of other genetically and antigenically related phleboviruses. The sensitivity of the assay was compared to that of a previously published TaqMan RTD-PCR protocol and found to be equal. Similarly, the assay demonstrated very high diagnostic sensitivity and specificity in various clinical human and animal specimens, collected during natural outbreaks of the disease in Africa. The detection of specific viral genome targets in positive clinical specimens was achieved in less than 30 minutes. As a highly accurate, rapid and very simple nucleic acid detection format, the RT-LAMP assay has the potential to be used in less well equipped laboratories in Africa. The assay format can be adapted to a portable device that can be utilized during RVF outbreaks in remote areas, and can be a valuable tool for differential diagnosis of VHFs. Microbiology and Plant Pathology unrestricted 2013-09-07T14:32:44Z 2010-10-22 2013-09-07T14:32:44Z 2010-09-02 2010-10-22 2010-10-22 Dissertation Le Roux, CA 2010, Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus, MSc dissertation, University of Pretoria, Pretoria, viewed yymmdd < http://hdl.handle.net/2263/28948 > E10/731/gm http://hdl.handle.net/2263/28948 http://upetd.up.ac.za/thesis/available/etd-10222010-181950/ © 2010, 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 Rift Valley fever (RVF)
Viral haemorrhagic fevers (VHFs)
Rift Valley fever virus (RVFV)
UCTD
Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title_full Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title_fullStr Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title_full_unstemmed Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title_short Real-time loop-mediated isothermal amplification assay for rapid detection of Rift Valley fever virus
title_sort real time loop mediated isothermal amplification assay for rapid detection of rift valley fever virus
topic Rift Valley fever (RVF)
Viral haemorrhagic fevers (VHFs)
Rift Valley fever virus (RVFV)
UCTD
url http://hdl.handle.net/2263/28948
http://upetd.up.ac.za/thesis/available/etd-10222010-181950/