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Recombinase polymerase amplification assay for rapid detection of Francisella tularensis.


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.

SUBMITTER: Euler M 

PROVIDER: S-EPMC3405570 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

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Recombinase polymerase amplification assay for rapid detection of Francisella tularensis.

Euler Milena M   Wang Yongjie Y   Otto Peter P   Tomaso Herbert H   Escudero Raquel R   Anda Pedro P   Hufert Frank T FT   Weidmann Manfred M  

Journal of clinical microbiology 20120418 7


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 PC  ...[more]

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