Department of Food Science, University of Arkansas System Division of Agriculture, Fayetteville, AR, USA.
Department of Animal Science, University of Arkansas System Division of Agriculture, Fayetteville, AR, USA.
J Food Prot. 2024 May;87(5):100252. doi: 10.1016/j.jfp.2024.100252. Epub 2024 Mar 13.
Sous-videcooking is a growing trend among retailers and consumers. Foodborne pathogens may survive the cooking if nonvalidated parameters are used or if pathogens have enhanced thermalresistance. Pathogen inactivation from sous-vide cooking was determined when introduced directly to beef products or via contaminated spices, and with or without a finishing step. Beef products (ground beef, tenderized, and nontenderized steaks) were inoculated with pathogens (Salmonella Montevideo and Escherichia coli O157:NM) in three ways: 1) directly onto the meat 2) ground black pepper incorporated into the recipe 3) ground pepper equilibrated at 30% RH (4 d) prior to incorporation. Beef samples were vacuum-packaged and submerged in a 62.5°C water bath for 120 min. Samples were sampled at 5, 10, 20, and 120 min (recommended from a partner quality study), and a duplicate was grilled to a specific internal temperature (74°C for ground beef, 57°C for steaks) and sampled. Sous-vide cooking reduced pathogen populations by >5 log CFU/g after most treatment times, but less than grilled counterparts (ca. 1-2 log CFU/g difference; p < 0.05).There were no statistically significant differences between inoculation methods, but the tenderization of steaks resulted in significantly lower reductions of pathogens from sous-vide cooking (p < 0.05). Thisresearch challenged sous-vide cooking parameters (120 min, 62.5°C). It showed sous-vide alone lowered pathogens by >4 log CFU/g after most 20-min treatments, but 120-min sous-vide treatments or grilling would be needed for >5-log reductions.Contaminated pepper led to less consistent reductions during the cooking process, yet 2-h sous-vide still achieved a 5-log reduction. Sous-vide cooking instructions must be validated as more products and recipes are marketed.
低温慢煮是零售商和消费者中日益流行的趋势。如果使用未经验证的参数或如果病原体具有增强的耐热性,则食品中的病原体可能在烹饪后存活下来。通过直接引入牛肉产品或通过污染的香料,以及是否有最后一步来确定低温慢煮烹饪中的病原体失活。牛肉产品(碎牛肉、嫩化和非嫩化牛排)以三种方式接种病原体(沙门氏菌蒙特利尔和大肠杆菌 O157:NM):1)直接在肉上 2)配方中加入黑胡椒粉 3)在加入之前在 30% RH(4 天)下平衡的黑胡椒粉。牛肉样品用真空包装并浸入 62.5°C 的水浴中 120 分钟。在 5、10、20 和 120 分钟时取样(来自合作伙伴质量研究的推荐时间),并将一个重复样烤至特定的内部温度(碎牛肉为 74°C,牛排为 57°C)并取样。在大多数处理时间后,低温慢煮可使病原体减少 >5 log CFU/g,但少于烧烤对照物(约 1-2 log CFU/g 差异;p<0.05)。接种方法之间没有统计学上的显着差异,但牛排的嫩化导致从低温慢煮中减少病原体的效果明显降低(p<0.05)。这项研究挑战了低温慢煮参数(120 分钟,62.5°C)。结果表明,在大多数 20 分钟处理后,单独的低温慢煮可使病原体减少 >4 log CFU/g,但需要 120 分钟的低温慢煮处理或烧烤才能减少 >5 个对数。在烹饪过程中,污染的胡椒粉导致减少效果不一致,但 2 小时的低温慢煮仍可实现 5 个对数的减少。随着更多产品和食谱推向市场,低温慢煮烹饪说明必须经过验证。