Kodaka Hidemasa, Teramura Hajime, Mizuochi Shingo, Saito Mikako, Matsuoka Hideaki
Research Institute of Advanced Technology, Nissui Pharmaceutical Co. Ltd., Yuki, Ibaraki 307-0036, Japan.
J Food Prot. 2009 Jan;72(1):169-73. doi: 10.4315/0362-028x-72.1.169.
Compact Dry VP (CDVP) is a ready-to-use method for enumerating Vibrio parahaemolyticus in food. The presterilized plates contain a culture medium comprising peptone, NaCl, bile salts, antibiotics, chromogenic substrates, and polysaccharide gum as a cold water-soluble gelling. After diluting raw seafood samples in a phosphate-buffered saline solution, a 1-ml aliquot was inoculated onto the center of the plate and allowed to diffuse by capillary action. Blue-green colonies forming on the plates were counted after 18 to 20 h of incubation at 35 degrees C. A total of 85 V. parahaemolyticus strains (62 tdh+ strains and 23 tdh- strains) were studied for inclusivity, 81 (95.3 %) of which produced blue-green colonies. When 97 strains (14 strains of Vibrio spp., 33 strains of coliform bacteria, and 50 strains of noncoliform bacteria) were assessed for exclusivity, 10 strains of Vibrio spp. produced non-blue-green colonies, and 87 strains failed to grow. The CDVP and U.S. Food and Drug Administration Bacteriological Analytical Manual (FDA-BAM) methods were compared with the use of four different types of raw seafood that were inoculated with four different V. parahaemolyticus strains. For raw tuna and oysters, the FDA-BAM colony lift method was used, whereas the FDA-BAM most-probable-number method was used for salmon and scallop. The linear correlation coefficients between the CDVP and FDA-BAM methods were 0.99 for fresh raw tuna, 0.95 for fresh raw oysters, 0.95 for frozen raw salmon, and 0.95 for frozen raw scallops. These results suggest that the CDVP method is useful for screening raw seafood for V. parahaemolyticus.
紧凑型干式VP(CDVP)是一种用于食品中副溶血性弧菌计数的即用型方法。预灭菌平板含有一种培养基,该培养基包含蛋白胨、氯化钠、胆盐、抗生素、显色底物和作为冷水溶性胶凝剂的多糖胶。将生海鲜样品在磷酸盐缓冲盐溶液中稀释后,取1毫升等分试样接种到平板中央,使其通过毛细作用扩散。在35℃孵育18至20小时后,对平板上形成的蓝绿色菌落进行计数。共研究了85株副溶血性弧菌菌株(62株tdh+菌株和23株tdh-菌株)的包容性,其中81株(95.3%)产生了蓝绿色菌落。当对97株菌株(14株弧菌属菌株、33株大肠菌群细菌和50株非大肠菌群细菌)进行排他性评估时,10株弧菌属菌株产生了非蓝绿色菌落,87株未生长。使用接种了四种不同副溶血性弧菌菌株的四种不同类型的生海鲜,对CDVP方法和美国食品药品监督管理局细菌学分析手册(FDA-BAM)方法进行了比较。对于生金枪鱼和牡蛎,使用FDA-BAM菌落提升法,而对于三文鱼和扇贝,则使用FDA-BAM最大可能数法。CDVP方法与FDA-BAM方法之间的线性相关系数,新鲜生金枪鱼为0.99,新鲜生牡蛎为0.95,冷冻生三文鱼为0.95,冷冻生扇贝为0.95。这些结果表明,CDVP方法可用于筛查生海鲜中的副溶血性弧菌。