Gense Kristina, Peterseil Verena, Licina Alma, Wagner Martin, Cichna-Markl Margit, Dobrovolny Stefanie, Hochegger Rupert
Austrian Competence Centre for Feed and Food Quality, Safety and Innovation, FFoQSI GmbH, Technopark 1, 3430 Tulln an der Donau, Austria.
Austrian Agency for Health and Food Safety (AGES), Institute for Food Safety, Department of Molecular Biology and Microbiology, Spargelfeldstr. 191, 1220 Vienna, Austria.
Foods. 2021 Oct 28;10(11):2618. doi: 10.3390/foods10112618.
The production of bivalve species has been increasing in the last decades. In spite of strict requirements for species declaration, incorrect labelling of bivalve products has repeatedly been detected. We present a DNA metabarcoding method allowing the identification of bivalve species belonging to the bivalve families Mytilidae (mussels), Pectinidae (scallops), and Ostreidae (oysters) in foodstuffs. The method, developed on Illumina instruments, targets a 150 bp fragment of mitochondrial 16S rDNA. We designed seven primers (three primers for mussel species, two primers for scallop species and a primer pair for oyster species) and combined them in a triplex PCR assay. In each of eleven reference samples, the bivalve species was identified correctly. In ten DNA extract mixtures, not only the main component (97.0-98.0%) but also the minor components (0.5-1.5%) were detected correctly, with only a few exceptions. The DNA metabarcoding method was found to be applicable to complex and processed foodstuffs, allowing the identification of bivalves in, e.g., marinated form, in sauces, in seafood mixes and even in instant noodle seafood. The method is highly suitable for food authentication in routine analysis, in particular in combination with a DNA metabarcoding method for mammalian and poultry species published recently.
在过去几十年中,双壳贝类的产量一直在增加。尽管对物种申报有严格要求,但仍多次检测到双壳贝类产品的标签错误。我们提出了一种DNA宏条形码方法,可用于识别食品中属于贻贝科(贻贝)、扇贝科(扇贝)和牡蛎科(牡蛎)的双壳贝类物种。该方法基于Illumina仪器开发,靶向线粒体16S rDNA的150 bp片段。我们设计了七种引物(三种用于贻贝物种的引物、两种用于扇贝物种的引物和一对用于牡蛎物种的引物),并将它们组合在一个三重PCR分析中。在11个参考样本中,每个样本中的双壳贝类物种都被正确识别。在10个DNA提取物混合物中,不仅主要成分(97.0 - 98.0%)被正确检测到,而且次要成分(0.5 - 1.5%)也大多被正确检测到,只有少数例外。发现DNA宏条形码方法适用于复杂和加工食品,能够识别例如腌制形式、酱汁中、海鲜混合物中甚至方便面海鲜中的双壳贝类。该方法非常适合常规分析中的食品认证,特别是与最近发表的一种用于哺乳动物和家禽物种的DNA宏条形码方法相结合时。