Articles
Rapid detection of apple stem grooving virus from reverse transcription recombinase polymerase amplification with a lateral flow dipstick (RT-RPA-LFD)
Article number
1401_38
Pages
255 – 262
Language
English
Abstract
Apple stem grooving virus (ASGV) is one of the most widespread and asymptomatic main viruses, that restrict the production of apple in the world.
Establishment of rapid, simple, and effective early detection method of apple viruses is important.
In this study, we established a one-step reverse transcription – recombinase polymerase amplification (RT-RPA) method, using the target-specific primers of ASGV coat protein gene sequence, and M-MLV reverse transcriptase.
This method could be completed within 30 min at 40°C, followed by a visual detection of the results within 5 min by using lateral flow dipstick (LFD). The specificity results showed that only samples infected with ASGV showed a test line, while no test line appeared in the ASGV-negative samples.
In addition, when crude extract of leaves was used, the whole detection could be completed within 1 h, which was shortened by 4 to 6 times as compared with RT-PCR method.
The detection made on more field samples showed that the RT-RPA-LFD method is of high stability and reliability for ASGV diagnosis, with a great potential in the rapid on-site detection of plant viruses.
Establishment of rapid, simple, and effective early detection method of apple viruses is important.
In this study, we established a one-step reverse transcription – recombinase polymerase amplification (RT-RPA) method, using the target-specific primers of ASGV coat protein gene sequence, and M-MLV reverse transcriptase.
This method could be completed within 30 min at 40°C, followed by a visual detection of the results within 5 min by using lateral flow dipstick (LFD). The specificity results showed that only samples infected with ASGV showed a test line, while no test line appeared in the ASGV-negative samples.
In addition, when crude extract of leaves was used, the whole detection could be completed within 1 h, which was shortened by 4 to 6 times as compared with RT-PCR method.
The detection made on more field samples showed that the RT-RPA-LFD method is of high stability and reliability for ASGV diagnosis, with a great potential in the rapid on-site detection of plant viruses.
Authors
X.Y. Ma, J.H. Bao, J.W. Li, X. Cheng, M.M. Tahir, M.Z. Liu, X. Lu, M.R. Wang, Z.B. Hamborg, D. Zhang
Keywords
apple stem grooving virus, reverse transcription – recombinase polymerase amplification, lateral flow dipstick, virus detection
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