rpoS 유전자를 대상으로 하는 Real-Time PCR에 의한 Vibrio vulnificus 검출

Detection of Vibrio vulnificus by Real-Time PCR targeted to rpoS gene

  • 김동균 (부경대학교 수산과학대학 생물공학과) ;
  • 안선희 (부경대학교 수산과학대학 생물공학과) ;
  • 배주윤 (부경대학교 수산과학대학 생물공학과) ;
  • 공인수 (부경대학교 수산과학대학 생물공학과)
  • Kim, Dong-Gyun (Department of Biotechnology, Pukyong National University) ;
  • Ahn, Sun-Hee (Department of Biotechnology, Pukyong National University) ;
  • Bae, Ju-Yoon (Department of Biotechnology, Pukyong National University) ;
  • Kong, In-Soo (Department of Biotechnology, Pukyong National University)
  • 발행 : 2007.12.31

초록

Vibrio vulnificusis a causative agent of serious diseases in humans resulting from the contact of wound with seawater or consumption of raw seafood. Several studies aimed at detecting V. vulnificus have targeted vvh as a representative virulence toxin gene belonging to the bacterium. In this study, we targeted the rpoS gene, a general stress regulator, to detect V. vulnificus. PCR specificity was identified by amplification of 8 V. vulnificus templates and by the loss of a PCR product with 36 non-V. vulnificus strains. The PCR assay had the 273-bp fragment and the sensitivity of 10 pg DNA from V. vulnificus. SYBR Green I-based real-time PCR assay targeting the rpoS gene showed a melting temperature of approximately $84^{\circ}C$ for V. vulnificus strains. The minimum level of detection by real-time PCR was 2 pg of purified genomic DNA, or $10^3$ V. vulnificus cells from pure cultured broth and $10^3$ cells in 1g of oyster tissue homogenates. These data indicate that real-time PCR is a sensitive, species-specific, and rapid method for detecting this bacterium using the rpoS gene in pure cultures and in infected oyster tissues.

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