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验证用于控制沙门氏菌和单核细胞增生李斯特菌的传统意大利式萨拉米香肠制造工艺。

Validation of a traditional Italian-style salami manufacturing process for control of Salmonella and Listeria monocytogenes.

作者信息

Nightingale K K, Thippareddi H, Phebus R K, Marsden J L, Nutsch A L

机构信息

Department of Animal Sciences & Industry and Food Science Institute, Kansas State University, Manhattan 66506, USA.

出版信息

J Food Prot. 2006 Apr;69(4):794-800. doi: 10.4315/0362-028x-69.4.794.

DOI:10.4315/0362-028x-69.4.794
PMID:16629021
Abstract

Italian-style salami batter (formulated with pork shoulder) was inoculated with ca. 7.0 log CFU/g of either Salmonella or Listeria monocytogenes. Salami links (55-mm cellulose casings) were fermented at 30 degrees C for 24, 40, or 72 h and then dried to target moisture/protein ratios (MPRs) of 1.9:1 or 1.4:1. Links were sampled after fermentation (24, 40, and 72 h) and after combined fermentation-drying treatments (MPRs of 1.9:1 and 1.4:1 for all fermentation periods), and microbiological and proximate analyses were performed at each sampling. Pathogen populations were enumerated by direct plating on selective agar and by an injured-cell recovery method. When enumerated by the injured-cell recovery method, Salmonella populations were reduced by 1.2 to 2.1 log CFU/g after fermentation alone (24 to 72 h) and by 2.4 to 3.4 log CFU/g when fermentation was followed by drying. Drying to an MPR of 1.4:1 was no more effective than drying to an MPR of 1.9:1 (P > 0.05). When enumerated directly on selective media, Salmonella populations were reduced from 1.6 to 2.4 log CFU/g and from 3.6 to 4.5 log CFU/g for fermentation alone and fermentation followed by drying, respectively. L. monocytogenes populations were reduced by <1.0 log CFU/g following all fermentation and combined fermentation-drying treatments, regardless of the enumeration method. These results suggest that the Italian-style salami manufacturing process evaluated does not adequately reduce high pathogen loads. Processors may thus need to consider supplemental measures, such as raw material specifications and a final heating step, to enhance the lethality of the overall manufacturing process.

摘要

将意大利风味萨拉米香肠糊(用猪肩肉配制)接种约7.0 log CFU/g的沙门氏菌或单核细胞增生李斯特菌。萨拉米香肠肠衣(55毫米纤维素肠衣)在30℃下发酵24、40或72小时,然后干燥至目标水分/蛋白质比(MPR)为1.9:1或1.4:1。在发酵后(24、40和72小时)以及发酵-干燥联合处理后(所有发酵期的MPR为1.9:1和1.4:1)对肠衣进行采样,并在每次采样时进行微生物学和近似分析。通过在选择性琼脂上直接平板计数和损伤细胞恢复方法来计数病原菌数量。当通过损伤细胞恢复方法计数时,仅发酵(24至72小时)后沙门氏菌数量减少1.2至2.1 log CFU/g,发酵后干燥时减少2.4至3.4 log CFU/g。干燥至MPR为1.4:1并不比干燥至MPR为1.9:1更有效(P>0.05)。当在选择性培养基上直接计数时,仅发酵和发酵后干燥时沙门氏菌数量分别从1.6至2.4 log CFU/g和3.6至4.5 log CFU/g减少。无论计数方法如何,在所有发酵以及发酵-干燥联合处理后,单核细胞增生李斯特菌数量减少<1.0 log CFU/g。这些结果表明,所评估的意大利风味萨拉米香肠制造工艺不能充分降低高病原菌负荷。因此,加工商可能需要考虑补充措施,如原材料规格和最终加热步骤,以提高整个制造工艺的致死率。

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