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A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus

Foot-and-mouth disease (FMD) is a trans-boundary viral disease of livestock, which causes huge economic losses and constitutes a serious infectious threat for livestock farming worldwide. Early diagnosis of FMD helps to diminish its impact by adequate outbreak management. In this study, we describe...

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Autores principales: Abd El Wahed, Ahmed, El-Deeb, Ayman, El-Tholoth, Mohamed, Abd El Kader, Hanaa, Ahmed, Abeer, Hassan, Sayed, Hoffmann, Bernd, Haas, Bernd, Shalaby, Mohamed A., Hufert, Frank T., Weidmann, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748043/
https://www.ncbi.nlm.nih.gov/pubmed/23977101
http://dx.doi.org/10.1371/journal.pone.0071642
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author Abd El Wahed, Ahmed
El-Deeb, Ayman
El-Tholoth, Mohamed
Abd El Kader, Hanaa
Ahmed, Abeer
Hassan, Sayed
Hoffmann, Bernd
Haas, Bernd
Shalaby, Mohamed A.
Hufert, Frank T.
Weidmann, Manfred
author_facet Abd El Wahed, Ahmed
El-Deeb, Ayman
El-Tholoth, Mohamed
Abd El Kader, Hanaa
Ahmed, Abeer
Hassan, Sayed
Hoffmann, Bernd
Haas, Bernd
Shalaby, Mohamed A.
Hufert, Frank T.
Weidmann, Manfred
author_sort Abd El Wahed, Ahmed
collection PubMed
description Foot-and-mouth disease (FMD) is a trans-boundary viral disease of livestock, which causes huge economic losses and constitutes a serious infectious threat for livestock farming worldwide. Early diagnosis of FMD helps to diminish its impact by adequate outbreak management. In this study, we describe the development of a real-time reverse transcription recombinase polymerase amplification (RT-RPA) assay for the detection of FMD virus (FMDV). The FMDV RT-RPA design targeted the 3D gene of FMDV and a 260 nt molecular RNA standard was used for assay validation. The RT-RPA assay was fast (4–10 minutes) and the analytical sensitivity was determined at 1436 RNA molecules detected by probit regression analysis. The FMDV RT-RPA assay detected RNA prepared from all seven FMDV serotypes but did not detect classical swine fever virus or swine vesicular disease virus. The FMDV RT-RPA assay was used in the field during the recent FMD outbreak in Egypt. In clinical samples, reverse transcription polymerase chain reaction (RT-PCR) and RT-RPA showed a diagnostic sensitivity of 100% and 98%, respectively. In conclusion, FMDV RT-RPA was quicker and much easier to handle in the field than real-time RT-PCR. Thus RT-RPA could be easily implemented to perform diagnostics at quarantine stations or farms for rapid spot-of-infection detection.
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spelling pubmed-37480432013-08-23 A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus Abd El Wahed, Ahmed El-Deeb, Ayman El-Tholoth, Mohamed Abd El Kader, Hanaa Ahmed, Abeer Hassan, Sayed Hoffmann, Bernd Haas, Bernd Shalaby, Mohamed A. Hufert, Frank T. Weidmann, Manfred PLoS One Research Article Foot-and-mouth disease (FMD) is a trans-boundary viral disease of livestock, which causes huge economic losses and constitutes a serious infectious threat for livestock farming worldwide. Early diagnosis of FMD helps to diminish its impact by adequate outbreak management. In this study, we describe the development of a real-time reverse transcription recombinase polymerase amplification (RT-RPA) assay for the detection of FMD virus (FMDV). The FMDV RT-RPA design targeted the 3D gene of FMDV and a 260 nt molecular RNA standard was used for assay validation. The RT-RPA assay was fast (4–10 minutes) and the analytical sensitivity was determined at 1436 RNA molecules detected by probit regression analysis. The FMDV RT-RPA assay detected RNA prepared from all seven FMDV serotypes but did not detect classical swine fever virus or swine vesicular disease virus. The FMDV RT-RPA assay was used in the field during the recent FMD outbreak in Egypt. In clinical samples, reverse transcription polymerase chain reaction (RT-PCR) and RT-RPA showed a diagnostic sensitivity of 100% and 98%, respectively. In conclusion, FMDV RT-RPA was quicker and much easier to handle in the field than real-time RT-PCR. Thus RT-RPA could be easily implemented to perform diagnostics at quarantine stations or farms for rapid spot-of-infection detection. Public Library of Science 2013-08-20 /pmc/articles/PMC3748043/ /pubmed/23977101 http://dx.doi.org/10.1371/journal.pone.0071642 Text en © 2013 Abd El Wahed et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Abd El Wahed, Ahmed
El-Deeb, Ayman
El-Tholoth, Mohamed
Abd El Kader, Hanaa
Ahmed, Abeer
Hassan, Sayed
Hoffmann, Bernd
Haas, Bernd
Shalaby, Mohamed A.
Hufert, Frank T.
Weidmann, Manfred
A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title_full A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title_fullStr A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title_full_unstemmed A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title_short A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
title_sort portable reverse transcription recombinase polymerase amplification assay for rapid detection of foot-and-mouth disease virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748043/
https://www.ncbi.nlm.nih.gov/pubmed/23977101
http://dx.doi.org/10.1371/journal.pone.0071642
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