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Effects of Technological Processes on the Tenacity and Inactivation of Norovirus Genogroup II in Experimentally Contaminated Foods▿

机译:工艺流程对实验污染食品中诺如病毒基因组II的强度和灭活的影响▿

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摘要

Contaminated food is a significant vehicle for human norovirus transmission. The present study determined the effect of physicochemical treatments on the tenacity of infective human norovirus genogroup II in selected foods. Artificially contaminated produce was subjected to a number of processes used by the food industry for preservation and by the consumer for storage and preparation. Virus recovery was carried out by using ultrafiltration and was monitored by using bacteriophage MS2 as an internal process control. Norovirus was quantified by using monoplex one-step TaqMan real-time reverse transcription (RT)-PCR and an external standard curve based on recombinant RNA standards. An RNase pretreatment step was used to avoid false-positive PCR results caused by accessible RNA, which allowed detection of intact virus particles. Significant reductions in titers were obtained with heat treatments usually applied by consumers for food preparation (baking, cooking, roasting). Generally, processes used for preservation and storage, such as cooling, freezing, acidification (≥pH 4.5), and moderate heat treatments (pasteurization), appear to be insufficient to inactivate norovirus within a food matrix or on the surface of food. Besides data for persistence in processed food, comparable data for individual matrix-specific protective effects, recovery rates, and inhibitory effects on the PCRs were obtained in this study. The established procedure might be used for other noncultivable enteric RNA viruses that are connected to food-borne diseases. The data obtained in this study may also help optimize the process for inactivation of norovirus in food by adjusting food processing technologies and may promote the development of risk assessment systems in order to improve consumer protection.
机译:被污染的食物是人类诺如病毒传播的重要媒介。本研究确定了理化处理对选定食品中感染性人类诺如病毒基因组II的韧性的影响。人为污染的产品要经过食品工业用于保存以及消费者用于存储和制备的许多过程。通过超滤进行病毒回收,并通过噬菌体MS2作为内部过程控制进行监控。诺如病毒通过单步TaqMan实时逆转录(RT)-PCR和基于重组RNA标准的外标曲线进行定量。使用RNase预处理步骤可避免由可及RNA引起的假阳性PCR结果,从而可检测完整的病毒颗粒。消费者通常通过食品加工(烘烤,烹饪,烧烤)进行的热处理,可显着降低滴度。通常,用于保存和存储的过程,例如冷却,冷冻,酸化(≥pH 4.5)和适度的热处理(巴氏灭菌),似乎不足以灭活食物基质内或食物表面上的诺如病毒。除了在加工食品中的持久性数据外,在这项研究中还获得了各个基质特异性保护作用,回收率和对PCR的抑制作用的可比较数据。既定程序可用于与食源性疾病有关的其他不可培养的肠RNA病毒。通过调整食品加工技术,从这项研究中获得的数据还可以帮助优化食品中诺如病毒的灭活过程,并可以促进风险评估系统的发展,以改善对消费者的保护。

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