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groEL is a suitable genetic marker for detecting Vibrio parahaemolyticus by loop-mediated isothermal amplification assay.
Siddique, M P; Jang, W J; Lee, J M; Ahn, S H; Suraiya, S; Kim, C H; Kong, I S.
Afiliação
  • Siddique MP; Department of Biotechnology, Pukyong National University, Busan, Korea.
  • Jang WJ; Department of Biotechnology, Pukyong National University, Busan, Korea.
  • Lee JM; Department of Biotechnology, Pukyong National University, Busan, Korea.
  • Ahn SH; Department of Oral Biochemistry, Dental Science Research Institute, Medical Research Center for Biomineralization Disorders, School of Dentistry, Chonnam National University, Gwangju, Korea.
  • Suraiya S; Department of Biotechnology, Pukyong National University, Busan, Korea.
  • Kim CH; Department of Marine Bio-materials & Aquaculture, Pukyong National University, Busan, Korea.
  • Kong IS; Department of Biotechnology, Pukyong National University, Busan, Korea.
Lett Appl Microbiol ; 65(2): 106-113, 2017 Aug.
Article em En | MEDLINE | ID: mdl-28585379
ABSTRACT
A groEL gene-based loop-mediated isothermal amplification (LAMP) assay was developed to detect Vibrio parahaemolyticus in contaminated seafood and water. The assay was optimized and conducted at 63°C for 40 min using Bacillus stearothermophilus (Bst) DNA polymerase, large fragment. Amplification was analysed via multiple detection methods, including opacity, formation of white precipitate, DNA intercalating dyes (ethidium bromide and SYBR Green I), metal ion-binding indicator dye, calcein, and 2% agarose gel electrophoresis. A characteristic ladder-like band pattern on agarose gel and the desired colour changes when using different dyes were observed in positive cases, and these were species-specific for V. parahaemolyticus when compared with other closely related Vibrio spp. The limit of detection (LoD) of this assay was 100 fg per reaction, 100-fold higher than that for conventional polymerase chain reaction (PCR). When tested on artificially contaminated seafood and seawater, the LoDs of the LAMP assay were 120 and 150 fg per reaction respectively, and those of conventional PCR were 120 and 150 pg per reaction respectively. Based on our results, the groEL gene-based LAMP assay is rapid, specific, sensitive, and reliable for detecting V. parahaemolyticus, and it could be used in field diagnosis. SIGNIFICANCE AND IMPACT OF THE STUDY The loop-mediated isothermal amplification (LAMP) assay using groEL gene (an abundant, highly conserved gene and member of the groESL chaperone gene family) provided rapid, species-specific and highly sensitive method for detecting Vibrio parahaemolyticus, the leading causal agent of seafood-borne diseases worldwide. Moreover, groEL LAMP revealed high efficiency than conventional PCR assay for V. parahaemolyticus using template both from pure culture and artificially contaminated seafood and water, which indicated the applicability in the field and environmental screening purpose for the organism.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vibrio parahaemolyticus / Alimentos Marinhos / Chaperonina 60 / Doenças Transmitidas por Alimentos Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vibrio parahaemolyticus / Alimentos Marinhos / Chaperonina 60 / Doenças Transmitidas por Alimentos Tipo de estudo: Diagnostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article