Andronache Julia, Cichna-Markl Margit, Dobrovolny Stefanie, Hochegger Rupert
Department of Molecular Biology and Microbiology, Institute for Food Safety, Austrian Agency for Health and Food Safety (AGES), Spargelfeldstraße 191, 1220 Vienna, Austria.
Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria.
Foods. 2025 Apr 28;14(9):1549. doi: 10.3390/foods14091549.
Seafood is a valuable commodity with increasing demand, traded for billions of USD each year. The volatility in supply chains and fluctuating prices contribute to the susceptibility of the seafood market to food fraud. Analytical methods are required to identify seafood in processed foods to ensure food authenticity and compliance with European laws. To address this need, we developed and validated a DNA metabarcoding method for the authentication of crustaceans and cephalopods in processed food samples, as both are prone to food fraud, especially in mixed products. A ~200 bp barcode of the mitochondrial 16S rDNA was selected as the marker for identification and sequenced on Illumina platforms. The DNA metabarcoding method utilizes two primer systems, one for the amplification of crustacean DNA and another for cephalopods. The crustacean primer system comprises two forward and two reverse primers, while the cephalopod primer system includes three forward and one reverse primer. DNA extracts from reference materials, model foods, processed foodstuffs, and DNA extract mixtures were investigated. Even species with a close phylogenetic relationship were successfully identified and differentiated in commercial samples, while single species were detected at amounts as low as 0.003% in model foods. However, false-negative results were obtained for certain species in DNA extract mixtures, which are most likely due to degraded or low-quality DNA and can best be prevented by optimized DNA extraction procedures. Our DNA metabarcoding method demonstrates strong potential as a qualitative screening tool in combination with other in-house DNA metabarcoding methods for food authentication in routine analysis.
海鲜是一种需求不断增长的珍贵商品,每年的交易额达数十亿美元。供应链的波动和价格的起伏导致海鲜市场容易出现食品欺诈行为。需要采用分析方法来鉴定加工食品中的海鲜,以确保食品的真实性并符合欧洲法律。为满足这一需求,我们开发并验证了一种DNA宏条形码方法,用于鉴定加工食品样品中的甲壳类动物和头足类动物,因为这两类动物都容易出现食品欺诈问题,尤其是在混合产品中。选择线粒体16S rDNA的一个约200 bp的条形码作为鉴定标记,并在Illumina平台上进行测序。DNA宏条形码方法使用两种引物系统,一种用于扩增甲壳类动物的DNA,另一种用于扩增头足类动物的DNA。甲壳类动物引物系统包括两条正向引物和两条反向引物,而头足类动物引物系统包括三条正向引物和一条反向引物。对参考材料、模拟食品、加工食品和DNA提取物混合物的DNA提取物进行了研究。即使是亲缘关系密切的物种也能在商业样品中成功鉴定和区分,而在模拟食品中,单个物种的检测量低至0.003%。然而,在DNA提取物混合物中某些物种出现了假阴性结果,这很可能是由于DNA降解或质量低所致,通过优化DNA提取程序可以最好地避免这种情况。我们的DNA宏条形码方法与其他内部DNA宏条形码方法相结合,在常规分析中作为食品鉴定的定性筛选工具显示出强大的潜力。