Institute of Marine Industry, Department of Seafood Science and Technology, Gyeongsang National University, Tongyeong 53064, Republic of Korea.
West Sea Fisheries Research Institute, National Institute of Fisheries Science, Incheon 22383, Republic of Korea.
Viruses. 2023 Jul 21;15(7):1599. doi: 10.3390/v15071599.
Human norovirus (HuNoV) is a common cause of outbreaks linked to food. In this study, the effectiveness of a non-thermal method known as high-pressure processing (HPP) on the viable reduction of an HuNoV GII.4 strain on raw crabs was evaluated at three different pressures (200, 400, and 600 MPa). HuNoV viability in raw crabs was investigated by using propidium monoazide/sarkosyl (PMA) as a nucleic acid intercalating dye prior to performing a real-time reverse transcription-polymerase chain reaction (RT-qPCR). The effect of the HPP exposure on pH, sensory, and Hunter colors were also assessed. HuNoV was reduced in raw crabs compared with control to HPP (0.15-1.91 log) in non-PMA and (0.67-2.23 log) in PMA. HuNoV genomic titer reduction was <2 log copy number/µL) when HPP was treated for 5 min without PMA pretreatment, but it was reduced to >2 log copy number/µL after PMA. The pH and Hunter colors of the untreated and HPP-treated raw crabs were significantly different ( < 0.05), but sensory attributes were not significant. The findings indicate that PMA/RT-qPCR could be used to detect HuNoV infectivity without altering the quality of raw crabs after a 5 min treatment with HPP. Therefore, HuNoV GII.4 could be reduced up to 2.23 log in food at a commercially acceptable pressure duration of 600 MPa for 5 min.
人类诺如病毒(HuNoV)是与食物有关的暴发的常见原因。在这项研究中,评估了一种称为高压处理(HPP)的非热方法在三种不同压力(200、400 和 600 MPa)下对生蟹中 HuNoV GII.4 株的存活减少的效果。在进行实时逆转录聚合酶链反应(RT-qPCR)之前,使用吖啶橙/沙克索利(PMA)作为核酸嵌入染料来研究生蟹中 HuNoV 的活力。还评估了 HPP 暴露对 pH 值、感官和亨特颜色的影响。与对照相比,未经 PMA 预处理的 HPP(0.15-1.91 log)和 PMA 中的 HPP(0.67-2.23 log)减少了生蟹中的 HuNoV。当 HPP 处理 5 分钟而没有 PMA 预处理时,HuNoV 基因组滴度减少<2 log 拷贝数/µL,但 PMA 后减少到>2 log 拷贝数/µL。未经处理和 HPP 处理的生蟹的 pH 值和亨特颜色有显著差异(<0.05),但感官属性没有显著差异。研究结果表明,PMA/RT-qPCR 可用于检测 HuNoV 感染性,而不会改变 HPP 处理 5 分钟后生蟹的质量。因此,在 600 MPa 的商业可接受压力持续时间为 5 分钟的情况下,可将食品中的 HuNoV GII.4 减少 2.23 log。