Gatto Francesco, Savini Christian, Sacco Maria Grazia, Vinciguerra Daniela, Buttinger Gerhard, Corbisier Philippe, Mazzara Marco, Emons Hendrik
European Commission, Joint Research Centre (JRC), Via Enrico Fermi 2749, 21027, Ispra, (VA), Italy.
European Commission, Joint Research Centre (JRC), Retieseweg 111, 2440, Geel, Belgium.
Food Control. 2022 Oct;140:109117. doi: 10.1016/j.foodcont.2022.109117.
The authorisation of genetically modified food and feed in the EU is subject to the provision of evidence of safety and of the availability of reliable analytical methods. These methods represent an essential tool for official laboratories to enforce a harmonised market control. Here the validation of droplet digital PCR (dPCR) methods has been performed for studying if the performance and acceptance parameters set by EU and other international guidelines for the analysis of genetically modified organisms (GMO) in food and feed are suitable and achievable also with such methods. The single-laboratory validation study showed that performance requirements set for GMO analysis by real time PCR can also be used to assess dPCR-based methods. Moreover, trueness and precision were assessed for both simplex and duplex formats in a multi-laboratory validation study organised according to international standards. Overall, the data on trueness, repeatability and reproducibility precision resulting from the collaborative study are satisfying the acceptance criteria for the respective parameters as stipulated in the EU and other international guidance such as the Codex Committee on Methods of Analysis and Sampling (CCMAS). For instance, the duplex droplet dPCR method for MON810 showed relative repeatability standard deviations from 1.8% to 15.7%, while the relative reproducibility standard deviation was found to be between 2.1% and 16.5% over the dynamic range studied. Moreover, the relative bias of the dPCR methods was well below 25% across the entire dynamic range. In addition, other aspects supporting the application of digital PCR for the control of GMOs on the market were experimentally assessed such as the conversion of the measurement results from copy number ratio to mass fraction, the influence of the DNA extraction step and of the ingredient content. It was found that the DNA extraction step added only a limited contribution to the variability of the measurement results under the studied conditions. The decreasing amount of the target ingredient content may decrease the level of precision of the method, although within the acceptance range of GMO performance parameters.
欧盟对转基因食品和饲料的授权需提供安全证据以及可靠分析方法的可用性。这些方法是官方实验室实施统一市场监管的重要工具。在此,已对液滴数字PCR(dPCR)方法进行了验证,以研究欧盟和其他国际准则为食品和饲料中转基因生物(GMO)分析设定的性能和验收参数是否也适用于此类方法以及是否可实现。单实验室验证研究表明,实时PCR为转基因生物分析设定的性能要求也可用于评估基于dPCR的方法。此外,在按照国际标准组织的多实验室验证研究中,对单重和双重格式的准确性和精密度进行了评估。总体而言,合作研究得出的准确性、重复性和再现性精密度数据符合欧盟和其他国际指南(如分析和采样方法法典委员会(CCMAS))中规定的各自参数的验收标准。例如,用于MON810的双重液滴dPCR方法的相对重复性标准偏差在1.8%至15.7%之间,而在所研究的动态范围内,相对再现性标准偏差在2.1%至16.5%之间。此外,dPCR方法的相对偏差在整个动态范围内远低于25%。此外,还通过实验评估了支持数字PCR用于市场上转基因生物控制的其他方面,如测量结果从拷贝数比转换为质量分数、DNA提取步骤的影响以及成分含量的影响。结果发现,在所研究的条件下,DNA提取步骤对测量结果的变异性贡献有限。目标成分含量的减少可能会降低该方法的精密度水平,尽管仍在转基因生物性能参数的验收范围内。