Stopforth Jarret D, Ikeda Jack S, Kendall Patricia A, Sofos John N
Department of Animal Sciences, Colorado State University, Fort Collins, CO 80523-1171, USA.
Int J Food Microbiol. 2004 Jan 1;90(1):51-61. doi: 10.1016/s0168-1605(03)00171-5.
This study evaluated survival/growth of acid-adapted or nonadapted Escherichia coli O157:H7 inoculated (4 log CFU/wound) in wounds (10 mm deepx6 mm diameter) of apples. Wounds were inoculated with a green fluorescent protein (GFP)-expressing derivative of a rifampicin-resistant strain of E. coli O157:H7 ATCC 43895 and allowed to attach (1 h). Apples were dipped (2 min) in solutions (approximately 25 degrees C) of water (W), 5% acetic acid (AA), 5% hydrogen peroxide (HP), 0.02% sodium hypochlorite (SH), or not treated (NT), and stored at 25 degrees C. Survivors were determined in cores (10-mm deep) of the apple wounds (12 mm from center of wound; inner core) and surrounding tissue (18 mm from center of wound; outer core) after homogenizing the samples in Dey-Engley (D/E) neutralizing broth and plating on tryptic soy agar (TSA) and TSA supplemented with 100 microg/ml rifampicin (35 degrees C, 48 h) after 0, 2 and 5 days. Average bacterial populations at day-0 were 4.0 and 2.0 logs in the inner and outer core, respectively. In the inner core of the untreated apples populations increased to 7.0 logs at day-2, while counts did not exceed 3.0 logs in the outer core during storage of all treatments. Previous acid-adaptation of the cultures did not affect survival of the pathogen. Dipping in W, AA and SH did not reduce initial bacterial populations, while at day-2 of storage inner core counts from W, AA and SH reached 7.1, 5.5 and 6.9 logs, respectively. In contrast, HP reduced initial counts in the inner core by approximately 1.5 logs, but they increased to 7.0 logs by day-2. Populations of all treatments reached 6.6-7.2 logs in the inner core by day-5. Thus, sanitizer treatment did not effectively reduce nor inhibit growth of E. coli O157:H7 contamination in apple wounds and surrounding tissue.
本研究评估了接种于苹果伤口(深10毫米×直径6毫米)中的酸适应性或非适应性大肠杆菌O157:H7(接种量为4 log CFU/伤口)的存活/生长情况。伤口接种了表达绿色荧光蛋白(GFP)的耐利福平大肠杆菌O157:H7 ATCC 43895菌株衍生物,并使其附着1小时。将苹果浸入(2分钟)水(W)、5%乙酸(AA)、5%过氧化氢(HP)、0.02%次氯酸钠(SH)溶液(约25摄氏度)中,或不进行处理(NT),然后在25摄氏度下储存。在0、2和5天后,将样品在戴伊 - 恩格利(D/E)中和肉汤中匀浆,然后接种于胰蛋白胨大豆琼脂(TSA)和添加了100微克/毫升利福平的TSA(35摄氏度,48小时)上,以测定苹果伤口核心(距伤口中心12毫米;内芯)和周围组织(距伤口中心18毫米;外芯)中的存活菌数。第0天内芯和外芯的平均细菌数量分别为4.0 log和2.0 log。在未处理苹果的内芯中,细菌数量在第2天增加到7.0 log,而在所有处理的储存期间,外芯中的菌数均未超过3.0 log。培养物先前的酸适应对病原体的存活没有影响。浸入水、乙酸和次氯酸钠溶液中并未降低初始细菌数量,而在储存第2天时,水、乙酸和次氯酸钠溶液处理的内芯菌数分别达到7.1 log、5.5 log和6.9 log。相比之下,过氧化氢使内芯中的初始菌数减少了约1.5 log,但在第2天时增加到7.0 log。到第5天时,所有处理的内芯菌数均达到6.6 - 7.2 log。因此,消毒剂处理未能有效减少或抑制苹果伤口及其周围组织中大肠杆菌O157:H7污染的生长。