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首页> 外文期刊>The New Microbiologica >Norovirus detection in shellfish using two Real-Time RT-PCR methods
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Norovirus detection in shellfish using two Real-Time RT-PCR methods

机译:使用两种实时RT-PCR方法检测贝类中的诺如病毒

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摘要

Shellfish are recognized as a potential vehicle of viral diseases. The aim of the present study was to determine the ability of two real-time RT-PCR methods (an in-house method and a commercial kit) for detecting Norovirus (NoV) belonging to genogroups GI and GII in shellfish. The analyses were performed both on a Norovirus Reference Panel (NRP), consisting of synthetic RNA, and on naturally contaminated mussels. For the experiments carried out on the NRP a statistically significant difference (chi(2)=8.03) was shown between the results obtained by the two methods. The in-house real-time RT-PCR allowed the detection of all genotypes belonging to GI and GII, while the commercial kit was not suitable for the detection of the majority of the GI sequences constituting the panel. No significant difference was instead detected in the experiments carried out on shellfish, where the presence of GI was always concomitant with GII. Both methods were suitable for detection of NoV in shellfish, however the in-house real-time RT-PCR method had the advantage of differentiating GI and GII contamination. As regards the shellfish analysed, a considerable frequency of NoV contamination (34.4% of the samples) was detected, with a predominance of NoV GII.
机译:贝类被认为是病毒性疾病的潜在媒介。本研究的目的是确定两种实时RT-PCR方法(内部方法和商业试剂盒)检测贝类中属于基因组GI和GII的诺如病毒(NoV)的能力。分析是在由合成RNA组成的诺如病毒参考面板(NRP)和天然受污染的贻贝上进行的。对于在NRP上进行的实验,两种方法获得的结果之间显示出统计学上的显着差异(chi(2)= 8.03)。内部实时RT-PCR允许检测属于GI和GII的所有基因型,而商用试剂盒不适合检测构成该组的大部分GI序列。相反,在对贝类进行的实验中未检测到显着差异,其中GI的存在总是与GII伴随的。两种方法都适用于检测贝类中的NoV,但是内部实时RT-PCR方法具有区分GI和GII污染的优势。对于分析的贝类,检测到相当高的NoV污染频率(占样本的34.4%),其中以NoV GII占多数。

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