Cheong Sooryun, Lee Cheonghoon, Choi Weon Cheon, Lee Chan-Hee, Kim Sang-Jong
School of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul 151-747, South Korea.
J Food Prot. 2009 Sep;72(9):2001-5. doi: 10.4315/0362-028x-72.9.2001.
Enteric viruses are the major cause of outbreaks of foodborne viral disease worldwide, and vegetables and fruits are considered significant vectors of virus transmission. In this study, we compared viral elution concentration methods in strawberry and lettuce and tested the secondary concentration step for concentrating viruses from large volumes of lettuce samples. Among the tested procedures, the combination of a 0.05 M glycine plus 100 mM Tris elution buffer (pH 9.5) and a polyethylene glycol precipitation concentration was most efficient for the detection of norovirus genogroup II from strawberries (50% of samples) and lettuce (2.9% of samples). The secondary concentration step using ultrafiltration devices could be applied to large lettuce samples without any decrease in detection limit and efficiency, and other cultivable enteric viruses including enteroviruses, adenoviruses, and rotaviruses were recovered from lettuce at efficiencies of 11.4, 9.05, and 11.3%, respectively. This method could be useful for detecting enteric viruses in fresh foods.
肠道病毒是全球食源性病毒病暴发的主要原因,蔬菜和水果被认为是病毒传播的重要载体。在本研究中,我们比较了草莓和生菜中病毒洗脱浓缩方法,并测试了从大量生菜样品中浓缩病毒的二次浓缩步骤。在所测试的方法中,0.05M甘氨酸加100mM Tris洗脱缓冲液(pH 9.5)和聚乙二醇沉淀浓缩相结合,对于从草莓(50%的样品)和生菜(2.9%的样品)中检测诺如病毒II基因组最为有效。使用超滤装置的二次浓缩步骤可应用于大量生菜样品,且检测限和效率均无任何降低,从生菜中回收其他可培养肠道病毒(包括肠道病毒、腺病毒和轮状病毒)的效率分别为11.4%、9.05%和11.3%。该方法可用于检测新鲜食品中的肠道病毒。