首页> 外文期刊>Journal of applied microbiology >Effectiveness of cooking to reduce Norovirus and infectious F-specific RNA bacteriophage concentrations in Mytilus edulis.
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Effectiveness of cooking to reduce Norovirus and infectious F-specific RNA bacteriophage concentrations in Mytilus edulis.

机译:烹饪的效果可降低可食用的Mytilus edulis中的诺如病毒和传染性F特异性RNA噬菌体浓度。

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Aims: 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. Methods and Results: Mussels ( n=600) contaminated with NoV and FRNA bacteriophage underwent four different cooking experiments performed in triplicate at ~70掳C and >90掳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 log 10 PFU g -1) in mussels were not significantly reduced in simmering water (~70掳C); however, cooking at higher temperatures (>90掳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掳C to be 42 s therefore a >3-log reduction in infectious virus can be obtained by heating mussel digestive tissue to 90掳C for 126 s. Conclusions: 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. Significance and Impact of the Study: The data will contribute towards evidence-based cooking recommendations for shellfish to provide a safe product for human consumption.
机译:目的:本研究的目的是确定家庭烹饪方法是否可以降低受实验污染的贻贝中诺如病毒(NoV)和F特异性RNA(FRNA)噬菌体的浓度。方法和结果:受NoV和FRNA噬菌体污染的贻贝(n = 600)在〜70°C和> 90°C的温度下进行了四个不同的蒸煮实验。将感染性FRNA噬菌体的浓度(使用噬斑测定)与使用标准化RT-qPCR确定的FRNA噬菌体和NoV的浓度进行比较。在水中(〜70掳C),贻贝中感染性FRNA噬菌体的初始浓度(7.05 log 10 PFU g -1)没有显着降低;但是,在更高的温度(> 90°C)下烹饪,会在3分钟内将传染性FRNA噬菌体降至未检测到的水平。进一步的研究确定,将FRNA噬菌体在90掳C时1-log降低所需的时间为42 s,因此,通过将贻贝消化组织加热到90掳C 126 s,可以将感染性病毒> 3 log降低。结论:仅基于开壳的家庭烹饪方法并不能灭活贻贝中的传染性病毒,但是,在高温下烹饪贻贝可有效降低传染性病毒的浓度并降低消费者患病的风险。研究的意义和影响:这些数据将有助于为贝类提供循证烹饪建议,从而为人类食用提供安全的产品。

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