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

dc.bibliographiccitation.artnumbere71642
dc.bibliographiccitation.issue8
dc.bibliographiccitation.journalPLoS ONE
dc.bibliographiccitation.volume8
dc.contributor.authorAbd El Wahed, Ahmed
dc.contributor.authorEl-Deeb, Ayman
dc.contributor.authorEl-Tholoth, Mohamed
dc.contributor.authorAbd El Kader, Hanaa
dc.contributor.authorAhmed, Abeer
dc.contributor.authorHassan, Sayed
dc.contributor.authorHoffmann, Bernd
dc.contributor.authorHaas, Bernd
dc.contributor.authorShalaby, Mohamed A.
dc.contributor.authorHufert, Frank T.
dc.contributor.authorWeidmann, Manfred
dc.date.accessioned2018-11-07T09:21:11Z
dc.date.available2018-11-07T09:21:11Z
dc.date.issued2013
dc.description.abstractFoot-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.
dc.identifier.doi10.1371/journal.pone.0071642
dc.identifier.isi000324527300028
dc.identifier.pmid23977101
dc.identifier.purlhttps://resolver.sub.uni-goettingen.de/purl?gs-1/10753
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/29055
dc.item.fulltextWith Fulltext
dc.notes.internMerged from goescholar
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherPublic Library Science
dc.relation.issn1932-6203
dc.rightsCC BY 3.0
dc.rights.urihttps://creativecommons.org/licenses/by/3.0
dc.titleA Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dc.type.versionpublished_version
dspace.entity.typePublication

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