Hara-Kudo Y, Nishina T, Nakagawa H, Konuma H, Hasegawa J, Kumagai S
Department of Biomedical Food Research, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.
Appl Environ Microbiol. 2001 Dec;67(12):5819-23. doi: 10.1128/AEM.67.12.5819-5823.2001.
We have developed a new, effective procedure for detecting Vibrio parahaemolyticus in seafoods using enrichment and plating onto a chromogenic agar medium. Samples were cultured in salt Trypticase soy broth, which is a nonselective medium, and then a portion of the culture was cultured with salt polymyxin broth, which is a selective medium for V. parahaemolyticus. This two-step enrichment was more effective than the one-step enrichment in salt polymyxin broth alone. The enrichment cultures were then plated onto a new chromogenic agar containing substrates for beta-galactosidase. The V. parahaemolyticus colonies developed a purple color on this growth medium that distinguished them from other related bacterial strains. V. parahaemolyticus was isolated more frequently from naturally contaminated seafood samples using the chromogenic agar than thiosulfate citrate bile salts sucrose agar medium, which is currently used for the isolation of V. parahaemolyticus. Our findings suggest that this new enrichment and isolation scheme is more sensitive and accurate for identifying V. parahaemolyticus in seafood samples than previously used methods.
我们开发了一种新的有效方法,通过富集培养并接种到显色琼脂培养基上来检测海鲜中的副溶血性弧菌。样品先在盐胰蛋白胨大豆肉汤(一种非选择性培养基)中培养,然后取一部分培养物接种到盐多粘菌素肉汤(一种副溶血性弧菌的选择性培养基)中。这种两步富集法比仅在盐多粘菌素肉汤中进行一步富集更有效。然后将富集培养物接种到一种含有β-半乳糖苷酶底物的新型显色琼脂上。副溶血性弧菌菌落在此生长培养基上呈现紫色,这使其与其他相关细菌菌株区分开来。与目前用于分离副溶血性弧菌的硫代硫酸盐柠檬酸盐胆盐蔗糖琼脂培养基相比,使用显色琼脂从自然污染的海鲜样品中更频繁地分离出副溶血性弧菌。我们的研究结果表明,这种新的富集和分离方案在识别海鲜样品中的副溶血性弧菌方面比以前使用的方法更灵敏、准确。