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Detection and Growth of Enteropathogenic Escherichia coli in Soft Ripened Cheese

机译:软干酪中肠致病性大肠杆菌的检测和生长

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The organism most frequently encountered during the 1971 outbreak of enteropathogenic Escherichia coli (EPEC) in soft ripened cheese was a strain that failed to ferment lactose broth within 48 h. Since existing methods for E. coli are dependent upon fermentation of this sugar, such strains can remain undetected, particularly when present in low numbers. Therefore, a cultural testing procedure was developed to insure isolation of both lactose-positive and -negative strains. This method used GN broth, modified by substituting lactose and arabinose for glucose and D-mannitol, as an enrichment medium. MacConkey agar, used as a plating medium, was modified by substituting arabinose for half the lactose. The cultural procedure was used in conjunction with a fluorescent antibody method to screen cheese for the presence of presumptive enteropathogenic E. coli. Suspected isolates were subjected to further biochemical and serological testing and identified as members of specific serogroups. These methods were used for the analysis of over 2,000 wheels of cheese; over 10% of the samples tested were found to contain strains belonging to six different serogroups associated with diarrheal diseases. No attempt was made to confirm pathogenicity by in vivo tests. Enumeration of E. coli in cheese showed that numbers increased during storage. Cheese with less than 10 organisms/g initially increased to over 105 at room temperature and over 103 at 4 C within 10 days. With higher initial counts, levels up to 109 were found at 4 C. These studies showed that the high levels of E. coli encountered in these products cannot be used as a direct indicator of post-processing contamination.
机译:在1971年爆发的软性成熟干酪中肠致病性大肠杆菌(EPEC)时最常遇到的生物是无法在48小时内发酵乳糖肉汤的菌株。由于用于大肠杆菌的现有方法取决于这种糖的发酵,因此此类菌株可以保持未被检测到的状态,尤其是当数量很少时。因此,开发了文化测试程序以确保分离乳糖阳性和阴性菌株。该方法使用GN肉汤(通过用乳糖和阿拉伯糖代替葡萄糖和D-甘露糖醇修饰)作为富集培养基。通过用阿拉伯糖代替一半的乳糖对用作平板培养基的MacConkey琼脂进行了修饰。将培养程序与荧光抗体方法结合使用,以筛选奶酪中是否存在推定的肠致病性大肠杆菌。怀疑的分离物经过进一步的生化和血清学检测,并被鉴定为特定血清群的成员。这些方法用于分析超过2,000轮奶酪。发现超过10%的受测样品含有属于与腹泻病相关的六个不同血清群的菌株。没有尝试通过体内测试来确认致病性。对奶酪中的大肠杆菌进行计数表明,在储存过程中,大肠杆菌的数量增加了。少于10个生物/ g的奶酪最初在10天内在室温下增加到105以上,在4 C下增加到103以上。具有较高的初始计数,在4 C时发现高达109的水平。这些研究表明,这些产品中遇到的高水平大肠杆菌不能用作处理后污染的直接指标。

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