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Development of a diagnostic system to detect potato virus T using RT-PCR and nested PCR

감자T바이러스 검정을 위한 RT-PCR 및 Nested PCR 진단시스템 개발

  • Lee, Si Won (Environmental Infrastructure Research Department, National Institute of Environmental Research) ;
  • Shin, Yong-Gil (Incheon International Airport Regional Office, Animal and Plant Quarantine Agency) ;
  • Lee, Jin-Young (Incheon International Airport Regional Office, Animal and Plant Quarantine Agency) ;
  • Kim, Young-Suk (Yeongsan River Environment Research Center, National Institute of Environmental Research) ;
  • Yang, Mi Hee (Environmental Infrastructure Research Department, National Institute of Environmental Research) ;
  • Choi, In-Cheol (Environmental Infrastructure Research Department, National Institute of Environmental Research)
  • 이시원 (국립환경과학원 환경기반연구부) ;
  • 신용길 (농림축산검역본부 인천공항지역본부) ;
  • 이진영 (농림축산검역본부 인천공항지역본부) ;
  • 김영석 (국립환경과학원 영산강물환경연구소) ;
  • 양미희 (국립환경과학원 환경기반연구부) ;
  • 최인철 (국립환경과학원 환경기반연구부)
  • Received : 2015.03.30
  • Accepted : 2015.06.23
  • Published : 2015.06.30

Abstract

Potato virus T (PVT) is a plant pathogen in the family Betaflexiviridae, group IV single-stranded positive sense RNA viruses. The major host of PVT is potato, and it has been reported in Ullucus tuberosus, Oxalis tuberosa and Tropaeolum tuberosum. This study aimed at developing reverse transcription (RT)-polymerase chain reaction (PCR) and nested PCR techniques for specific detection of PVT. Finally, Two RT-PCR primer sets were developed and verified. The RT-PCR products were amplified to 734 (PVT RT-PCR primer set 6) and 828 bp (PVT RT-PCR primer set 29) long to detect PVT. The nested PCR primer sets [PVT-N70/C20 ($734{\rightarrow}315bp$) and PVT-N75/C30 ($828{\rightarrow}529bp$)] were developed which are high sensitivity and verification for detection of PVT. Furthermore, a modified-positive control plasmid is use to verify contamination of laboratory in PVT detection. This study supported the diagnose PVT in potato or PVT related hosts.

Keywords

References

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