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首页> 外文期刊>Food Control >MinION sequencing of seafood in Singapore reveals creatively labelled flatfishes, confused roe, pig DNA in squid balls, and phantom crustaceans
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MinION sequencing of seafood in Singapore reveals creatively labelled flatfishes, confused roe, pig DNA in squid balls, and phantom crustaceans

机译:新加坡海鲜的甲型序列显示出创造性标记的扁平鱼,困惑的獐鹿,鱿鱼球的猪DNA,以及幽灵甲壳类动物

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摘要

Food mislabelling is a growing world-wide problem that can be addressed through the authentication of ingredients via techniques like mass spectrometry or DNA sequencing. However, unfortunately traditional DNA sequencing methods are slow, expensive, and require well-equipped laboratories. We here test whether these problems can be overcome through the use of Nanopore sequencing. We sequenced 92 single and 13 mixed-species samples purchased in Singapore. We successfully obtained DNA barcodes for 94% and 100% of the single- and mixed-species samples respectively by applying a bioinformatics pipeline that was optimised for this purpose. We find comparatively low levels of clear-cut mislabelling for single-species samples (7.6%), while the rates are higher for mixed-species samples (38.5%). The low rates for single-species samples are somewhat deceptive, however, because of the use of vague species names. With regard to the clearly mislabelled single-species products, higher-value products (e.g., prawn roe, wild-caught Atlantic salmon, halibut) are replaced with lower-value ingredients (e.g., fish roe, Pacific salmon, arrowtooth flounder) while more serious problems are observed for mixed-species samples. Cuttlefish and prawn balls repeatedly contained pig DNA and all but one of the mixed samples labelled as containing crustaceans ('crab', 'prawn', 'lobster') lacked a significant number of crustacean signals. We conclude that there is a need for more regular testing of seafood samples and suggest that due to speed and low-cost, MinION would be a good instrument for this purpose. We also emphasize the need for developing clearer labelling guidelines.
机译:食物错误标记是一种日益增长的全球问题,可以通过质谱或DNA测序等技术通过成分的认证来解决。然而,遗憾的是,传统的DNA测序方法缓慢,昂贵,并且需要设备齐全的实验室。我们在这里通过使用纳米孔测序来测试这些问题是否可以克服。我们在新加坡购买的92个单身和13种混合物种样本。我们通过应用针对此目的优化的生物信息化管道,分别成功获得了DNA条形码94%和100%的单一和混合物种样品。我们发现单一物种样品的相对较低的透明误标标签(7.6%),而混合物种样品的速率较高(38.5%)。然而,由于使用模糊物种名称,单物种样本的低速率有点欺骗性。关于清晰的单一物种产品,高价值产品(例如,虾仁,野生捕获的大西洋鲑鱼,大比目鱼)被较低价值的成分(例如,鱼獐鹿,太平洋鲑鱼,箭头野生群)所取代对于混合物种样品,观察到严重问题。墨鱼和虾球反复含有猪DNA,除了含有甲壳类动物('蟹','虾','龙虾')的混合样品之外的所有混合样品缺乏大量的甲壳类动物信号。我们得出结论,需要更多地定期检测海鲜样本,并提出由于速度和低成本,矿井将为此目的是一个好的仪器。我们还强调需要开发更清晰的标签指南。

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