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食品中诺如病毒基因Ⅱ型热处理失活动力评估。

Evaluation of heat treatment for inactivation of norovirus genogroup II in foods.

机构信息

Laboratory of Comparative and Environmental Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation/FIOCRUZ, Rio de Janeiro, 21040-360, Brazil.

出版信息

Braz J Microbiol. 2022 Sep;53(3):1159-1165. doi: 10.1007/s42770-022-00731-3. Epub 2022 Mar 21.

Abstract

The effective food processing technology is a key step in eliminating human noroviruses in foods mainly due to their stability in diverse environmental conditions. The aim of this study was to evaluate the effect of rising temperatures for inactivation of norovirus genogroup (G) II and murine norovirus 1 in samples of tomato sauce (72-74 °C for 1 min) and ground meat (100 °C for 30 min). Spiking experiments were carried out in triplicate using TRIzol® reagent method associated with quantitative polymerase chain reaction (qPCR) TaqMan™ system combined with previous free RNA digestion. Success rate and efficiency recoveries of both viruses as well limit of detection of a method for each matrix were also conducted. The heat treatment applied here proved to be efficient to reduce the burden of norovirus GII in a range of 1-4 log genomic copies per gram (percentage ranging from 0.45 to 104.54%) in both matrices. The experiments in this study showed that the results of norovirus GII and murine norovirus 1 in tomato sauce and ground meat tested during thermal treatments cannot be generalized to other food matrices, since there may be food-specific protective effects, as the presence of different components, that can interfere in virus inactivation. Studies using different food matrices reinforce the importance to investigate viruses' inactivation thermal processes in foods due to the resistance of these viruses to adverse conditions, contributing to food security in food virology.

摘要

有效的食品加工技术是消除食品中人类诺如病毒的关键步骤,主要是因为它们在各种环境条件下都很稳定。本研究的目的是评估升高温度对番茄沙司(72-74°C 1 分钟)和绞碎肉(100°C 30 分钟)中诺如病毒基因群(G)II 和鼠诺如病毒 1 的灭活效果。使用 TRIzol®试剂方法进行了三重重复的加标实验,该方法与定量聚合酶链反应(qPCR)TaqMan™系统相结合,并结合了先前的游离 RNA 消化。还进行了两种病毒的成功率和效率回收率以及每种基质的方法检测限的检测。此处应用的热处理被证明可有效降低番茄沙司和绞碎肉中诺如病毒 GII 的负担,范围为每克 1-4 个基因组拷贝(百分比范围为 0.45-104.54%)。本研究中的实验表明,在热处理过程中测试的番茄沙司和绞碎肉中诺如病毒 GII 和鼠诺如病毒 1 的结果不能推广到其他食品基质,因为可能存在特定于食品的保护作用,因为存在不同的成分会干扰病毒的失活。使用不同食品基质的研究强调了在食品中调查病毒灭活热过程的重要性,因为这些病毒对不利条件具有抵抗力,这有助于食品病毒学中的食品安全。

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