Neunlist Margarida Ribeiro, Ralazamahaleo Mavo, Cappelier Jean-michel, Besnard Valérie, Federighi Michel, Leroi Françoise
Unité Mixte de Recherche Institut National de Recherche Agronomique Sécurité Alimentaire 1014, Ecole Nationale Vétérinaire de Nantes, Route de Gachet, BP 40706-44307 Nantes Cedex 03, France.
J Food Prot. 2005 Jan;68(1):85-91. doi: 10.4315/0362-028x-68.1.85.
The aim of the present study was to determine the effect of the different steps of the cold-smoking process and vacuum storage on the culturability and viability of Listeria monocytogenes strain Scott A inoculated in sterile salmon samples. Additionally, the virulence of L. monocytogenes cells was assessed by intravenous inoculation of immunocompetent mice. Salmon (Salmo salar) portions were inoculated with L. monocytogenes at a level of 6 log CFU/g and were then dry salted (5.9%), smoked (0.74 mg phenol per 100 g), partially frozen (-7 degrees C), vacuum packed, and stored for 10 days at 4 degrees C followed by 18 days at 8 degrees C. Salting represented the only step of the process with a weak but significant listericidal effect (0.6 log reduction). Although the other processing steps had no immediate reduction effect on L. monocytogenes, the combination of steps significantly lowered by 1.6 log CFU/g the number of L. monocytogenes. The culturable count remained less than 7 log CFU/g until the end of the storage period, whereas in unprocessed samples (control) the culturable counts reached values up to 9 log CFU/g. To mimic a postprocess contamination, salmon portions were also inoculated with L. monocytogenes after being cold-smoke processed. A reduction of the culturable count during the 2 first weeks of storage was observed, but then growth occurred and identical values observed for preprocess contamination were reached at the end of the storage. A viable but nonculturable state transition of strain Scott A was not observed, and the cold-smoking process did not affect the virulence of bacteria isolated at the beginning and end of the storage.
本研究的目的是确定冷熏过程的不同步骤以及真空储存对无菌三文鱼样本中接种的单核细胞增生李斯特菌菌株斯科特A的可培养性和活力的影响。此外,通过对免疫活性小鼠进行静脉接种来评估单核细胞增生李斯特菌细胞的毒力。将三文鱼(大西洋鲑)切块接种单核细胞增生李斯特菌,接种水平为6 log CFU/g,然后进行干盐腌制(5.9%)、烟熏(每100 g含0.74 mg苯酚)、部分冷冻(-7℃)、真空包装,并在4℃下储存10天,随后在8℃下储存18天。腌制是该过程中唯一具有微弱但显著杀李斯特菌效果(减少0.6 log)的步骤。尽管其他加工步骤对单核细胞增生李斯特菌没有立即的减少作用,但这些步骤的组合显著降低了单核细胞增生李斯特菌的数量,降低了1.6 log CFU/g。直到储存期结束,可培养菌数仍低于7 log CFU/g,而在未加工的样本(对照)中,可培养菌数达到了高达9 log CFU/g的值。为模拟加工后污染,三文鱼切块在冷熏加工后也接种了单核细胞增生李斯特菌。在储存的前两周观察到可培养菌数减少,但随后出现生长,在储存结束时达到了与加工前污染相同的值。未观察到斯科特A菌株向活的但不可培养状态的转变,冷熏过程也未影响储存开始和结束时分离出的细菌的毒力。