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Most-probable-number loop-mediated isothermal amplification-based procedure enhanced with K antigen-specific immunomagnetic separation for quantifying tdh(+) Vibrio parahaemolyticus in molluscan Shellfish.
Tanaka, Natsuko; Iwade, Yoshito; Yamazaki, Wataru; Gondaira, Fumio; Vuddhakul, Varaporn; Nakaguchi, Yoshitsugu; Nishibuchi, Mitsuaki.
Affiliation
  • Tanaka N; Graduate School of Medicine, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.
  • Iwade Y; Mie Prefecture Health and Environment Research Institute, Sakura-cho, Yokkaichi-shi, Mie 512-1211, Japan.
  • Yamazaki W; Department of Veterinary Science, Faculty of Agriculture, University of Miyazaki, Gakuenkibanadainishi, Miyazaki-shi, Miyazaki 889 2192, Japan.
  • Gondaira F; Denka Seiken Co., Ltd., Nihonbashi-Muromachi, Chuo-ku, Tokyo 103-8338, Japan.
  • Vuddhakul V; Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai 90110, Thailand.
  • Nakaguchi Y; Center for Southeast Asian Studies, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.
  • Nishibuchi M; Center for Southeast Asian Studies, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan. nisibuti@cseas.kyoto-u.ac.jp.
J Food Prot ; 77(7): 1078-85, 2014 Jul.
Article in En | MEDLINE | ID: mdl-24988012
Although thermostable direct hemolysin-producing (tdh(+)) Vibrio parahaemolyticus is the leading cause of seafood-borne gastroenteritis, the enumeration of tdh(+) V. parahaemolyticus remains challenging due to its low densities in the environment. In this study, we developed a most-probable-number (MPN)-based procedure designated A-IS(1)-LAMP, in which an immunomagnetic separation (IMS) technique targeting as many as 69 established K antigens and a loop-mediated isothermal amplification (LAMP) assay targeting the thermostable direct hemolysin (tdh) gene were applied in an MPN format. Our IMS employed PickPen, an eight-channel intrasolution magnetic particle separation device, which enabled a straightforward microtiter plate-based IMS procedure (designated as PickPen-IMS). The ability of the procedure to quantify a wide range of tdh(+) V. parahaemolyticus levels was evaluated by testing shellfish samples in Japan and southern Thailand, where shellfish products are known to contain relatively low and high levels of total V. parahaemolyticus, respectively. The Japanese and Thai shellfish samples showed, respectively, relatively low (< 3 to 11 MPN/10 g) and considerably higher (930 to 110,000 MPN/10 g) levels of tdh(+) V. parahaemolyticus, raising concern about the safety of Thai shellfish products sold to domestic consumers at local morning markets. LAMP showed similar or higher performance than conventional PCR in the detection and quantification of a wide range of tdh(+) V. parahaemolyticus levels in shellfish products. Whereas a positive effect of PickPen-IMS was not observed in MPN determination, PickPen-IMS was able to concentrate tdh(+) V. parahaemolyticus 32-fold on average from the Japanese shellfish samples at an individual tube level, suggesting a possibility of using PickPen-IMS as an optional tool for specific shellfish samples. The A-IS(1)-LAMP procedure can be used by any health authority in the world to measure the tdh(+) V. parahaemolyticus levels in shellfish products.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shellfish / Vibrio parahaemolyticus / Immunomagnetic Separation / Nucleic Acid Amplification Techniques / Mollusca / Antigens, Bacterial / Antigens, Surface Type of study: Evaluation_studies Limits: Animals / Humans Country/Region as subject: Asia Language: En Journal: J Food Prot Year: 2014 Document type: Article Affiliation country: Japan Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shellfish / Vibrio parahaemolyticus / Immunomagnetic Separation / Nucleic Acid Amplification Techniques / Mollusca / Antigens, Bacterial / Antigens, Surface Type of study: Evaluation_studies Limits: Animals / Humans Country/Region as subject: Asia Language: En Journal: J Food Prot Year: 2014 Document type: Article Affiliation country: Japan Country of publication: United States