Kim Ye Won, You Hyun Ju, Lee Soyoung, Kim Bomi, Kim Do Kyung, Choi Joo-Bong, Kim Ji-Ah, Lee Hee Jung, Joo In Sun, Lee Jeong Su, Kang Dong Hyun, Lee Giljae, Ko Gwang Pyo, Lee Sung-Joon
1 Department of Biotechnology, School of Life Sciences and Biotechnology for BK21 PLUS, Korea University, Seoul 02841, Republic of Korea.
2 Institute of Health and Environment, Department of Environmental Health, Center for Human and Environmental Microbiome, Graduate School of Public Health, Seoul National University, Seoul 151-742, Republic of Korea.
J Food Prot. 2017 Aug;80(8):1293-1302. doi: 10.4315/0362-028X.JFP-16-162.
This study investigated the effect of lemongrass essential oil (LGEO) on the infectivity and viral replication of norovirus. Murine norovirus 1 (MNV-1), a surrogate of human norovirus, was preincubated with LGEO and then used to infect RAW 264.7 cells in a plaque reduction assay. LGEO exhibited a significant reduction in MNV-1 plaque formation in both time- and dose-dependent manners. The quantification of viral genome by quantitative real-time PCR showed similar results in line with those of the plaque reduction assay. It was revealed that citral, a single compound in LGEO, showed dramatic reduction in MNV-1 infectivity (-73.09% when using a treatment of 0.02%, v/v). The inhibitory activity of LGEO on viral replication was further investigated in HG23 cells that harbored a human norovirus replicon. LGEO treatment significantly reduced viral replication in HG23 cells, which suggests that LGEO may have dual inhibitory activities that inactivate viral coat proteins required for viral infection and suppress norovirus genome replication in host cells. In animal experiments, oral administration of murine norovirus preincubated with LGEO significantly suppressed virus infectivity in vivo. Collectively, these results suggest that LGEO, in particular the LGEO component citral, inactivates the norovirus and its subsequent replication in host cells. Thus, LGEO shows promise as a method of inhibiting norovirus within the food industry.
本研究调查了柠檬草精油(LGEO)对诺如病毒感染性和病毒复制的影响。将小鼠诺如病毒1型(MNV-1,人类诺如病毒的替代物)与LGEO预孵育,然后用于在蚀斑减少试验中感染RAW 264.7细胞。LGEO在时间和剂量依赖性方式上均显著减少了MNV-1蚀斑形成。通过定量实时PCR对病毒基因组进行定量分析,结果与蚀斑减少试验结果相似。研究发现,LGEO中的单一化合物柠檬醛显著降低了MNV-1的感染性(当使用0.02%,v/v处理时降低了73.09%)。在携带人类诺如病毒复制子的HG23细胞中进一步研究了LGEO对病毒复制的抑制活性。LGEO处理显著降低了HG23细胞中的病毒复制,这表明LGEO可能具有双重抑制活性,即灭活病毒感染所需的病毒衣壳蛋白并抑制宿主细胞中的诺如病毒基因组复制。在动物实验中,口服与LGEO预孵育的小鼠诺如病毒可显著抑制体内病毒感染性。总体而言,这些结果表明LGEO,特别是LGEO成分柠檬醛,可使诺如病毒失活并抑制其在宿主细胞中的后续复制。因此,LGEO有望成为食品工业中抑制诺如病毒的一种方法。