The Plant Pathology Journal · 2011 · 22 citations · 12 references
AgriculturePlant BiologyPlant SciencesMolecular VirologyPlant VirologyVirologyPlant Virus DetectionPlant Virus QuarantinePlant VirusesViral Rna BiologyVirus-host InteractionsCapsid Protein DetectionPcr-based DetectionPolymerase Chain Reaction SpecificityPrimer DesignQuarantineQuarantine ProtocolsVirus Detection AssaysVirus Diseases
In order to detect quarantine plant viruses, we developed reverse transcription-polymerase chain reaction (RT-PCR) primer pairs for five single-stranded (ss) plant RNA viruses that are not currently reported in Korea but could be potential harmful plant viral pathogens. Three viruses such as Chilli veinal mottle virus (ChiVMV), Colombian datura virus (CDV), and Tobacco etch virus (TEV) belong to the genus Potyvirus while Chrysanthemum stem necrosis virus (CSNV) and Iris yellow spot virus (IYSV) are members of the genus Tospovirus. To design RT-PCR primers, we used reported gene sequences corresponding to the capsid protein and polyprotein for ChiVMV, CDV, and TEV while using nucleocapsid protein regions for CSNV and IYSV. At least two different primer pairs were designed for each virus. Fifteen out of 16 primer pairs were successfully applied in detection of individual quarantine virus with high specificity and efficiency. Taken together, this study provides a rapid and useful protocol for detection of five quarantine viruses.
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H. R. Pappu, Lindsey J. du Toit, Howard F. Schwartz et al. · Archives of Virology · 2005 · 49 citations