Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/18311
Appears in Collections:Aquaculture Journal Articles
Peer Review Status: Refereed
Title: Recombinase Polymerase Amplification Assay for Rapid Detection of Francisella tularensis
Author(s): Euler, Milena
Wang, Yongjie
Otto, Peter
Tomaso, Herbert
Escudero, Raquel
Anda, Pedro
Hufert, Frank T
Weidmann, Manfred
Contact Email: m.w.weidmann@stir.ac.uk
Issue Date: Jul-2012
Date Deposited: 14-Jan-2014
Citation: Euler M, Wang Y, Otto P, Tomaso H, Escudero R, Anda P, Hufert FT & Weidmann M (2012) Recombinase Polymerase Amplification Assay for Rapid Detection of Francisella tularensis. Journal of Clinical Microbiology, 50 (7), pp. 2234-2238. https://doi.org/10.1128/JCM.06504-11
Abstract: Several real-time PCR approaches to develop field detection for Francisella tularensis, the infectious agent causing tularemia, have been explored. We report the development of a novel qualitative real-time isothermal recombinase polymerase amplification (RPA) assay for use on a small ESEQuant Tube Scanner device. The analytical sensitivity and specificity were tested using a plasmid standard and DNA extracts from infected rabbit tissues. The assay showed a performance comparable to real-time PCR but reduced the assay time to 10 min. The rapid RPA method has great application potential for field use or point-of-care diagnostics.
DOI Link: 10.1128/JCM.06504-11
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