TY - JOUR
T1 - A one-step reverse transcriptase loop-mediated isothermal amplification assay for simple and rapid detection of swine vesicular disease virus
AU - Blomström, Anne-Lie
AU - Hakhverdyan, Mikhayil
AU - Reid, Scott M.
AU - Dukes, Juliet P.
AU - King, Donald P.
AU - Belák, Sándor
AU - Berg, Mikael
PY - 2008
Y1 - 2008
N2 - This report describes the development of a one-step reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) assay for the detection of swine vesicular disease virus (SVDV). The assay detects the virus rapidly, within 30-60 min and the result is visualised either by gel-electrophoresis or by the naked eye through the addition of SybrGreen. A collection of 28 SVDV isolates were tested positive, while heterologous viruses such as foot-and-mouth disease virus and vesicular stomatitis virus remained negative. The performance of the RT-LAMP was compared directly with real-time PCR using RNA from clinical samples including nasal swabs, serum and faeces. For nasal swabs and serum the sensitivity of the RT-LAMP was shown to be at least equivalent to real-time PCR. Interestingly, for faecal samples the RT-LAMP assay was shown to be even more sensitive than real-time PCR, possibly because it is less sensitive to inhibitory substances. This RT-LAMP assay provides a number of benefits for the diagnosis of SVD, since the assay is sensitive and rapid, and the isothermal amplification strategy used is not reliant upon expensive equipment it is particularly suited for "front line" diagnosis of SVD in modestly equipped laboratories, in field stations or in mobile diagnostic units. (C) 2007 Elsevier B.V. All rights reserved.
AB - This report describes the development of a one-step reverse transcriptase loop-mediated isothermal amplification (RT-LAMP) assay for the detection of swine vesicular disease virus (SVDV). The assay detects the virus rapidly, within 30-60 min and the result is visualised either by gel-electrophoresis or by the naked eye through the addition of SybrGreen. A collection of 28 SVDV isolates were tested positive, while heterologous viruses such as foot-and-mouth disease virus and vesicular stomatitis virus remained negative. The performance of the RT-LAMP was compared directly with real-time PCR using RNA from clinical samples including nasal swabs, serum and faeces. For nasal swabs and serum the sensitivity of the RT-LAMP was shown to be at least equivalent to real-time PCR. Interestingly, for faecal samples the RT-LAMP assay was shown to be even more sensitive than real-time PCR, possibly because it is less sensitive to inhibitory substances. This RT-LAMP assay provides a number of benefits for the diagnosis of SVD, since the assay is sensitive and rapid, and the isothermal amplification strategy used is not reliant upon expensive equipment it is particularly suited for "front line" diagnosis of SVD in modestly equipped laboratories, in field stations or in mobile diagnostic units. (C) 2007 Elsevier B.V. All rights reserved.
KW - swine vesicular disease virus
KW - loop-mediated isothermal amplification
KW - detection
KW - swine vesicular disease virus
KW - loop-mediated isothermal amplification
KW - detection
UR - https://res.slu.se/id/publ/20421
U2 - 10.1016/j.jviromet.2007.08.023
DO - 10.1016/j.jviromet.2007.08.023
M3 - Journal article
C2 - 17920701
SN - 0166-0934
VL - 147
SP - 188
EP - 193
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 1
ER -