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美国农业部食品安全检验局和美国食品药品监督管理局的《细菌学分析手册》培养方法、BBL CHROMagar沙门氏菌预制平板和迪夫科脱水培养基。

USDA FSIS and FDA BAM culture methods BBL CHROMagar Salmonella prepared plated and Difco dehydrated culture media.

作者信息

Ritter Vicki, Dick Nancy

机构信息

BD Diagnostic Systems, 250 Schilling Circle, Hunt Valley, MD 21030, USA.

出版信息

J AOAC Int. 2009 Mar-Apr;92(2):459-70.

PMID:19485205
Abstract

BBL and Difco CHROMagar Salmonella (CS) was evaluated internally and externally for the recovery of Salmonella in raw chicken, raw ground beef, raw fish, lettuce, and shell eggs. The raw chicken and ground beef were processed according to the U.S. Department of Agriculture, Food Safety and Inspection Service reference methods. The raw fish, lettuce, and shell eggs were processed according to the U.S. Food and Drug Administration, Bacteriological Analytical Manual procedures. Only raw chicken was found to be naturally contaminated with Salmonella; all other matrixes were seeded with an appropriate dilution of organism to achieve fractionally positive results. Salmonella strains were permitted to equilibrate with the culture-negative matrixes for 48 h at 4 degrees C. Twenty 25 g samples of each food matrix plus 5 uninoculated samples were processed. CS prepared plates (CS PPM) and laboratory prepared plates from dehydrated culture media (CS DCM) were evaluated with the reference method media. A total of 16 positive cultures were obtained from the raw chicken samples, 17 in the raw ground beef, 18 in the raw fish and lettuce, and 11 in the shell eggs. A Chi-square analysis was performed on each of the food matrixes. BBL CS produced comparable results with the reference methods on all matrixes, resulting in a method agreement of 100% based on the Chi-square results. In testing known isolates the sensitivity and specificity was determined to be 94%. Specificity improved to 98% when tetrathionate broth enrichment was used. A negative- and false-positive rate of 6% was found with known isolates. No false negatives were found in testing the food matrixes. The performance of the CS prepared plate and laboratory prepared plate was identical.

摘要

对 BBL 和 Difco CHROMagar 沙门氏菌显色培养基(CS)进行了内部和外部评估,以检测生鸡肉、生碎牛肉、生鱼、生菜和带壳鸡蛋中的沙门氏菌。生鸡肉和碎牛肉按照美国农业部食品安全与检验局的参考方法进行处理。生鱼、生菜和带壳鸡蛋按照美国食品药品监督管理局《细菌学分析手册》的程序进行处理。仅发现生鸡肉天然受到沙门氏菌污染;所有其他基质均接种适当稀释的菌液以获得部分阳性结果。沙门氏菌菌株在 4℃下与培养阴性的基质平衡 48 小时。对每种食品基质的 20 个 25 克样品加 5 个未接种样品进行处理。用参考方法培养基评估 CS 预制平板(CS PPM)和由脱水培养基在实验室制备的平板(CS DCM)。从生鸡肉样品中总共获得 16 个阳性培养物,生碎牛肉中 17 个,生鱼和生菜中 18 个,带壳鸡蛋中 11 个。对每种食品基质进行卡方分析。BBL CS 在所有基质上与参考方法产生了可比的结果,根据卡方结果,方法一致性为 100%。在检测已知分离株时,灵敏度和特异性被确定为 94%。当使用四硫磺酸钠肉汤增菌时,特异性提高到 98%。在检测已知分离株时,发现阴性率和假阳性率为 6%。在检测食品基质时未发现假阴性。CS 预制平板和实验室制备平板的性能相同。

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