Publication: A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus
| dc.bibliographiccitation.artnumber | e71642 | |
| dc.bibliographiccitation.issue | 8 | |
| dc.bibliographiccitation.journal | PLoS ONE | |
| dc.bibliographiccitation.volume | 8 | |
| dc.contributor.author | Abd El Wahed, Ahmed | |
| dc.contributor.author | El-Deeb, Ayman | |
| dc.contributor.author | El-Tholoth, Mohamed | |
| dc.contributor.author | Abd El Kader, Hanaa | |
| dc.contributor.author | Ahmed, Abeer | |
| dc.contributor.author | Hassan, Sayed | |
| dc.contributor.author | Hoffmann, Bernd | |
| dc.contributor.author | Haas, Bernd | |
| dc.contributor.author | Shalaby, Mohamed A. | |
| dc.contributor.author | Hufert, Frank T. | |
| dc.contributor.author | Weidmann, Manfred | |
| dc.date.accessioned | 2018-11-07T09:21:11Z | |
| dc.date.available | 2018-11-07T09:21:11Z | |
| dc.date.issued | 2013 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.1371/journal.pone.0071642 | |
| dc.identifier.isi | 000324527300028 | |
| dc.identifier.pmid | 23977101 | |
| dc.identifier.purl | https://resolver.sub.uni-goettingen.de/purl?gs-1/10753 | |
| dc.identifier.uri | https://resolver.sub.uni-goettingen.de/purl?gro-2/29055 | |
| dc.item.fulltext | With Fulltext | |
| dc.notes.intern | Merged from goescholar | |
| dc.notes.status | zu prüfen | |
| dc.notes.submitter | Najko | |
| dc.publisher | Public Library Science | |
| dc.relation.issn | 1932-6203 | |
| dc.rights | CC BY 3.0 | |
| dc.rights.uri | https://creativecommons.org/licenses/by/3.0 | |
| dc.title | A Portable Reverse Transcription Recombinase Polymerase Amplification Assay for Rapid Detection of Foot-and-Mouth Disease Virus | |
| dc.type | journal_article | |
| dc.type.internalPublication | yes | |
| dc.type.peerReviewed | yes | |
| dc.type.status | published | |
| dc.type.version | published_version | |
| dspace.entity.type | Publication |
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