Flessa Stephan, Lusk Dawn M, Harris Linda J
Department of Food Science and Technology, University of California, One Shields Ave., Davis, CA 95616-8598, USA.
Int J Food Microbiol. 2005 Jun 15;101(3):255-62. doi: 10.1016/j.ijfoodmicro.2004.11.010.
Cut or intact surfaces of fresh strawberries were spot inoculated with a five-strain cocktail of nalidixic-acid resistant Listeria monocytogenes (10(6) (low inoculum) and 10(8) (high inoculum) CFU per three-berry sample). Inoculated strawberries were dried for 1 h at 24 degrees C and were stored in loosely closed containers at 4 or 24 degrees C. An initial population reduction of approximately 0.6 and 1.2 log cycles, high and low inoculum, respectively, was observed on intact but not cut berries after the 1-h drying period. A decrease of 1.4 and 3.3 log cycles per intact sample was observed over 48 h for the high and low inoculum, respectively, when stored at 24 degrees C. When held at 4 degrees C, a reduction of approximately 3 log cycles per intact-berry sample was observed for both inocula over the 7-day storage period. Populations on cut surfaces remained constant at both temperatures and both inoculum densities throughout the storage period. Sliced, inoculated strawberries (6.7 log CFU/25-g sample) with or without 20% sucrose were frozen at -20+/-2 degrees C. After 28 days of frozen storage, populations of L. monocytogenes determined on tryptose phosphate agar supplemented with nalidixic acid (TPAN) had declined by 0 to 1.2 log cycles, with and without 20% sucrose, respectively. Counts on modified Oxford agar supplemented with nalidixic acid were significantly (P< or =0.05) lower (0.5 to 1.8 log CFU/g) than on TPAN indicating that some cell injury had occurred. Results of this study indicate that L. monocytogenes is capable of survival but not growth on the surface of fresh intact or cut strawberries throughout the expected shelf life of the fresh fruit and can survive on frozen strawberries for periods of at least 4 weeks. On whole strawberries held at 24 degrees C, significantly faster declines (P< or =0.05) of L. monocytogenes were observed when lower rather than higher inoculum levels were applied.
将耐萘啶酸的单核细胞增生李斯特菌的五菌株混合菌液(每三个草莓样品含10⁶(低接种量)和10⁸(高接种量)CFU)点接种于新鲜草莓的切割面或完整表面。接种后的草莓在24℃下干燥1小时,然后储存在敞口容器中,温度为4℃或24℃。在1小时干燥期后,在完整但未切割的草莓上观察到初始菌量分别减少了约0.6和1.2个对数循环,分别对应高接种量和低接种量。当储存在24℃时,高接种量和低接种量的完整样品在48小时内分别减少了1.4和3.3个对数循环。当保存在4℃时,在7天的储存期内,两种接种量的每个完整草莓样品的菌量均减少了约3个对数循环。在整个储存期内,切割面上的菌量在两种温度和两种接种密度下均保持恒定。将切片的接种草莓(6.7 log CFU/25-g样品),添加或不添加20%蔗糖,在-20±2℃下冷冻。冷冻储存28天后,在补充了萘啶酸的胰蛋白胨磷酸盐琼脂(TPAN)上测定的单核细胞增生李斯特菌菌量,添加和不添加20%蔗糖的情况下分别下降了0至1.2个对数循环。补充了萘啶酸的改良牛津琼脂上的计数显著(P≤0.05)低于TPAN上的计数(0.5至1.8 log CFU/g),表明发生了一些细胞损伤。本研究结果表明,在新鲜完整或切割草莓的表面,单核细胞增生李斯特菌在新鲜水果的预期货架期内能够存活但不能生长,并且在冷冻草莓上可以存活至少4周。在24℃保存的完整草莓上,当接种量较低而不是较高时,观察到单核细胞增生李斯特菌的下降速度明显更快(P≤0.05)。