Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification

Apple stem grooving virus (ASGV) is considered to cause the most economically important viral disease in pears in Korea. The current PCR-based methods used to diagnose ASGV are time-consuming in terms of target detection. In this study, a novel assay for specific ASGV detection that is based on reve...

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Main Authors: Nam-Yeon Kim, Jonghee Oh, Su-Heon Lee, Hongsup Kim, Jae Sun Moon, Rae-Dong Jeong
Format: Article
Language:English
Published: Hanrimwon Publishing Company 2018-12-01
Series:The Plant Pathology Journal
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305176
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spelling doaj-e657c9bfd5fd4d669bff27c984af10a22020-11-24T23:48:13ZengHanrimwon Publishing CompanyThe Plant Pathology Journal1598-22542018-12-0134657557910.5423/PPJ.NT.06.2018.010810.5423PPJ.NT.06.2018.0108Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase AmplificationNam-Yeon Kim0Jonghee Oh1Su-Heon Lee2Hongsup Kim3Jae Sun Moon4Rae-Dong Jeong5Department of Applied Biology, Institute of Environmentally Friendly Agriculture, Chonnam National University, Gwangju 61185, KoreaSchool of Applied Biosciences, Kyungpook National University, Daegu 98411, KoreaSchool of Applied Biosciences, Kyungpook National University, Daegu 98411, KoreaSeed Testing & Research Center, Korea Seed & Variety Service, Gimcheon, KoreaPlant Genome Research Center, Korea Research Institute of Bioscience & Biotechnology, Daejeon, KoreaDepartment of Applied Biology, Institute of Environmentally Friendly Agriculture, Chonnam National University, Gwangju 61185, KoreaApple stem grooving virus (ASGV) is considered to cause the most economically important viral disease in pears in Korea. The current PCR-based methods used to diagnose ASGV are time-consuming in terms of target detection. In this study, a novel assay for specific ASGV detection that is based on reverse transcription-recombinase polymerase amplification is described. This assay has been shown to be reproducible and able to detect as little as 4.7 ng/μl of purified RNA obtained from an ASGV-infected plant. The major advantage of this assay is that the reaction for the target virus is completed in 1 min, and amplification only requires an incubation temperature of 42°C. This assay is a promising alternative method for pear breeding programs or virus-free certification laboratories.http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305176Apple stem grooving virusmolecular diagnosisreverse transcription-recombinase polymerase amplification
collection DOAJ
language English
format Article
sources DOAJ
author Nam-Yeon Kim
Jonghee Oh
Su-Heon Lee
Hongsup Kim
Jae Sun Moon
Rae-Dong Jeong
spellingShingle Nam-Yeon Kim
Jonghee Oh
Su-Heon Lee
Hongsup Kim
Jae Sun Moon
Rae-Dong Jeong
Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
The Plant Pathology Journal
Apple stem grooving virus
molecular diagnosis
reverse transcription-recombinase polymerase amplification
author_facet Nam-Yeon Kim
Jonghee Oh
Su-Heon Lee
Hongsup Kim
Jae Sun Moon
Rae-Dong Jeong
author_sort Nam-Yeon Kim
title Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
title_short Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
title_full Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
title_fullStr Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
title_full_unstemmed Rapid and Specific Detection of Apple stem grooving virus by Reverse Transcription-recombinase Polymerase Amplification
title_sort rapid and specific detection of apple stem grooving virus by reverse transcription-recombinase polymerase amplification
publisher Hanrimwon Publishing Company
series The Plant Pathology Journal
issn 1598-2254
publishDate 2018-12-01
description Apple stem grooving virus (ASGV) is considered to cause the most economically important viral disease in pears in Korea. The current PCR-based methods used to diagnose ASGV are time-consuming in terms of target detection. In this study, a novel assay for specific ASGV detection that is based on reverse transcription-recombinase polymerase amplification is described. This assay has been shown to be reproducible and able to detect as little as 4.7 ng/μl of purified RNA obtained from an ASGV-infected plant. The major advantage of this assay is that the reaction for the target virus is completed in 1 min, and amplification only requires an incubation temperature of 42°C. This assay is a promising alternative method for pear breeding programs or virus-free certification laboratories.
topic Apple stem grooving virus
molecular diagnosis
reverse transcription-recombinase polymerase amplification
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305176
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