Devenish J A, Schiemann D A
Can J Microbiol. 1981 Sep;27(9):937-41. doi: 10.1139/m81-146.
An abbreviated procedure for the biochemical identification of Yersinia enterocolitica isolated from food enrichments on CIN (cefsulodin-irgasan-novobiocin) agar was investigated. A total of 170 colonies resembling Y. enterocolitica in colonial morphology and appearance on CIN agar were selected for identification using API strips. Ninety-three of these isolates were examined with the PathoTec ornithine decarboxylase, Voges-Proskauer, and urease test strips. The PathoTec urease strip alone was adequate for identification of all isolates of Y. enterocolitica. Christensen's urea agar was applied to the remaining 77 isolates and found less specific in the 1 isolate of Enterobacter agglomerans was urease positive along with 10 isolates of Y. enterocolitica. CIN agar is a highly specific medium for isolation of Y. enterocolitica, requiring only Kligler iron agar and urea slants for confirmation of presumptive colonies.
研究了一种从CIN(头孢磺啶-伊红-新生霉素)琼脂上的食品增菌培养物中分离出的小肠结肠炎耶尔森菌的生化鉴定简化程序。总共选择了170个在CIN琼脂上菌落形态和外观类似于小肠结肠炎耶尔森菌的菌落,使用API试条进行鉴定。其中93株分离株用PathoTec鸟氨酸脱羧酶、Voges-Proskauer和脲酶试条进行检测。仅PathoTec脲酶试条就足以鉴定所有小肠结肠炎耶尔森菌分离株。将克里斯滕森尿素琼脂应用于其余77株分离株,发现其特异性较差,因为1株聚团肠杆菌与10株小肠结肠炎耶尔森菌一样脲酶呈阳性。CIN琼脂是用于分离小肠结肠炎耶尔森菌的高度特异性培养基,仅需克氏铁琼脂和尿素斜面来确认可疑菌落。