Samadpour M, Liston J, Ongerth J E, Tarr P I
Institute for Food Science and Technology, School of Fisheries, University of Washington, Seattle 98195.
Appl Environ Microbiol. 1990 May;56(5):1212-5. doi: 10.1128/aem.56.5.1212-1215.1990.
The use of DNA probes for Shiga-like toxin I (SLT-I) and SLT-II for detection of SLT-producing Escherichia coli (SLTEC) in foods and calf fecal samples was evaluated. Enrichment cultures were prepared from food or fecal samples. Colonies formed by plating of enrichment cultures were probed for SLTEC by colony hybridization. Alternatively, enrichment cultures were analyzed for SLTEC presence by dot blot. The lowest detected concentration of SLTEC in sample homogenates inoculated with E. coli O157:H7 corresponded to 1.3 CFU/g of sample. Of the 44 food samples and 28 fecal samples from dairy calves tested by the colony hybridization method, 4 food samples, including ground beef, raw goat milk, blueberries, and surimi-based delicatessen salad, and 9 calf fecal samples were positive with the SLT probes. The dot blot technique yielded results within 48 h and can be used as a fast and sensitive method of detection for SLTEC in foods and calf fecal samples. The colony hybridization technique took 3 to 4 days but permits recovery of the positive colonies when desired.
对用于检测食品和犊牛粪便样本中产志贺样毒素大肠杆菌(SLTEC)的志贺样毒素I(SLT-I)和志贺样毒素II的DNA探针的使用进行了评估。从食品或粪便样本中制备富集培养物。通过菌落杂交法对富集培养物平板上形成的菌落进行产志贺样毒素大肠杆菌检测。或者,通过斑点印迹法分析富集培养物中是否存在产志贺样毒素大肠杆菌。接种大肠杆菌O157:H7的样本匀浆中产志贺样毒素大肠杆菌的最低检测浓度相当于每克样本1.3个菌落形成单位。通过菌落杂交法检测的44份食品样本和28份犊牛粪便样本中,4份食品样本,包括绞碎牛肉、生山羊奶、蓝莓和鱼糜熟食沙拉,以及9份犊牛粪便样本,志贺样毒素探针检测呈阳性。斑点印迹技术在48小时内得出结果,可作为食品和犊牛粪便样本中产志贺样毒素大肠杆菌的快速灵敏检测方法。菌落杂交技术需要3至4天,但在需要时可用于回收阳性菌落。