| Literature DB >> 30011183 |
Se Hee Lee1, Gna Ahn1, Myung-Su Kim2, Ok Chan Jeong3,4, Jong Hyun Lee4, Hyuck Gi Kwon4, Yang-Hoon Kim1, Ji-Young Ahn1.
Abstract
Apple Scar Skin Viroid (ASSVd), a nonprotein coding, circular RNA pathogen is relatively difficult to detect by immunoassay. We report here a one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay to improve selectivity for diagnostic use in detecting ASSVd in plants. ASSVd RT-LAMP was accelerated using loop primers and was found to be highly sensitive with a detection limit of 104 copies of cDNA-ASSVd within 30 min. Real-time LAMP and melting curve analysis could differentiate between the true-positive LAMP amplicons and false-positive nonspecific primer amplification products. The optimized RT-LAMP was then followed by the addition of nonthiolated AuNP:poly-adenine (A10)-ASSVd LAMP barcodes, showing a high authentication capacity with colorimetric changes. This type of barcoding assay is a potential alternative for rapid and multiple viroid diagnosis, providing for visible sensing in the field that can be applied to viroid-free planting.Entities:
Keywords: Apple scar skin viroid (ASSVd); LAMP-barcording assay; poly-adenine (A) tail; reverse transcription loop-mediated isothermal amplification (RT-LAMP); virus detection
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Year: 2018 PMID: 30011183 DOI: 10.1021/acscombsci.8b00022
Source DB: PubMed Journal: ACS Comb Sci ISSN: 2156-8944 Impact factor: 3.784