PLoS ONE (Jan 2013)

A portable reverse transcription recombinase polymerase amplification assay for rapid detection of foot-and-mouth disease virus.

  • Ahmed Abd El Wahed,
  • Ayman El-Deeb,
  • Mohamed El-Tholoth,
  • Hanaa Abd El Kader,
  • Abeer Ahmed,
  • Sayed Hassan,
  • Bernd Hoffmann,
  • Bernd Haas,
  • Mohamed A Shalaby,
  • Frank T Hufert,
  • Manfred Weidmann

DOI
https://doi.org/10.1371/journal.pone.0071642
Journal volume & issue
Vol. 8, no. 8
p. e71642

Abstract

Read online

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.