Hahm B-K, Bhunia A K
Department of Food Science, Molecular Food Microbiology Laboratory, Purdue University, West Lafayette, IN 47907-2009, USA.
J Appl Microbiol. 2006 May;100(5):1017-27. doi: 10.1111/j.1365-2672.2006.02814.x.
To study the reaction patterns of selected antibodies to Escherichia coli O157:H7, Salmonella enterica serotype Enteritidis and Listeria monocytogenes cells exposed to various environmental stresses.
Escherichia coli O157:H7, Salmonella Enteritidis and L. monocytogenes cells subjected to different environmental stress of temperatures (4 and 45 degrees C), NaCl (5.5%), oxidative stress (15 mmol(-1) H2O2), acidic pH (5.5) and ethanol (5%) for 3 h (short-term stress) or for 5 days (long-term stress) were analysed by ELISA and Western blotting. The ELISA results indicated that most stresses caused 12-16% reductions in reaction for anti-E. coli O157:H7 and 20-48% reductions for anti-Salmonella polyclonal antibodies during short-term stress, whereas the most stresses exhibited enhanced reaction (44-100% increase) with the anti-L. monocytogenes polyclonal antibody. During long-term stress exposure to combined stress conditions of pH 5.5, 3.5% NaCl at 12 degrees C or at 4 degrees C, antibody reactions to the three pathogens were highly variable with the combined stress at 4 degrees C showing the most reductions (8-40%). Likewise, there were about 18-59% reductions in antibody reactions with pathogens when cultured in hotdog samples with the combined stress conditions. Western blot analyses of crude cell surface antigens from both short- and long-term stressed cells revealed that the changes in antibody reactions observed in ELISA were either because of repression, expression or possible denaturation of antigens on the surface of cells.
Overall, the antibody reactions were significantly reduced in pathogens exposed to both short- and long-term environmental stresses in culture medium or in meat sample because of expression, repression or denaturation of specific antigens in cells.
In order to ensure the reliable detection of foodborne pathogens using antibody-based methods, the influence of stress on antibody reactions should be thoroughly examined and understood first as the physiological activities in cells are often altered in response to a stress.
研究特定抗体对暴露于各种环境压力下的大肠杆菌O157:H7、肠炎沙门氏菌和单核细胞增生李斯特菌细胞的反应模式。
通过酶联免疫吸附测定(ELISA)和蛋白质免疫印迹法(Western blotting)分析了大肠杆菌O157:H7、肠炎沙门氏菌和单核细胞增生李斯特菌细胞在不同环境压力下的情况,这些压力包括温度(4℃和45℃)、氯化钠(5.5%)、氧化应激(15 mmol(-1)过氧化氢)、酸性pH值(5.5)和乙醇(5%),处理时间为3小时(短期应激)或5天(长期应激)。ELISA结果表明,在短期应激期间,大多数压力导致抗大肠杆菌O157:H7的反应降低12 - 16%,抗沙门氏菌多克隆抗体的反应降低20 - 48%,而大多数压力使抗单核细胞增生李斯特菌多克隆抗体的反应增强(增加44 - 100%)。在长期应激下,暴露于pH 5.5、3.5%氯化钠、12℃或4℃的组合应激条件时,对这三种病原体的抗体反应变化很大,4℃的组合应激导致的反应降低最多(8 - 40%)。同样,在具有组合应激条件的热狗样品中培养时,与病原体的抗体反应降低了约18 - 59%。对短期和长期应激细胞的粗细胞表面抗原进行的蛋白质免疫印迹分析表明,ELISA中观察到的抗体反应变化是由于细胞表面抗原的抑制、表达或可能的变性。
总体而言,由于细胞中特定抗原的表达、抑制或变性,在培养基或肉类样品中暴露于短期和长期环境压力下的病原体中,抗体反应显著降低。
为了确保使用基于抗体的方法可靠地检测食源性病原体,首先应彻底检查和了解应激对抗体反应的影响,因为细胞中的生理活动通常会因应激而改变。