Flannery J, Rajko-Nenow P, Winterbourn J B, Malham S K, Jones D L
Bangor University, Bangor, UK.
J Appl Microbiol. 2014 Aug;117(2):564-71. doi: 10.1111/jam.12534. Epub 2014 Jun 2.
The aim of this study was to determine if domestic cooking practices can reduce concentrations of norovirus (NoV) and F-specific RNA (FRNA) bacteriophage in experimentally contaminated mussels.
Mussels (n = 600) contaminated with NoV and FRNA bacteriophage underwent four different cooking experiments performed in triplicate at 70°C and >90°C. Concentrations of infectious FRNA bacteriophage (using a plaque assay) were compared with concentrations of FRNA bacteriophage and NoV determined using a standardised RT-qPCR. Initial concentrations of infectious FRNA bacteriophage (7·05 log10 PFU g(-1) ) in mussels were not significantly reduced in simmering water (70°C); however, cooking at higher temperatures (>90°C) reduced infectious FRNA bacteriophage to undetected levels within 3 min. Further investigation determined the time required for a 1-log reduction of infectious FRNA bacteriophage at 90°C to be 42 s therefore a >3-log reduction in infectious virus can be obtained by heating mussel digestive tissue to 90°C for 126 s.
Domestic cooking practices based on shell opening alone do not inactivate infectious virus in mussels, however, cooking mussels at high temperatures is effective to reduce infectious virus concentrations and the risk of illness in consumers.
The data will contribute towards evidence-based cooking recommendations for shellfish to provide a safe product for human consumption.
本研究旨在确定家庭烹饪方法是否能降低实验性污染贻贝中诺如病毒(NoV)和F特异性RNA(FRNA)噬菌体的浓度。
用诺如病毒和FRNA噬菌体污染的贻贝(n = 600)在约70°C和>90°C下进行了四项不同的烹饪实验,每项实验重复三次。将传染性FRNA噬菌体的浓度(使用噬菌斑测定法)与使用标准化RT-qPCR测定的FRNA噬菌体和诺如病毒的浓度进行比较。贻贝中传染性FRNA噬菌体的初始浓度(7.05 log10 PFU g-1)在微沸水中(约70°C)没有显著降低;然而,在较高温度(>90°C)下烹饪3分钟内可将传染性FRNA噬菌体降低到检测不到的水平。进一步研究确定在90°C下使传染性FRNA噬菌体减少1个对数所需的时间为42秒,因此将贻贝消化组织加热到90°C 126秒可使传染性病毒减少>3个对数。
仅基于开口的家庭烹饪方法不能使贻贝中的传染性病毒失活,然而,高温烹饪贻贝可有效降低传染性病毒浓度和消费者患病风险。
这些数据将有助于为贝类提供基于证据的烹饪建议,以提供安全的供人类食用的产品。