Bavarian Health and Food Safety Authority (LGL) , Veterinärstrasse 2, D-85764 Oberschleissheim, Germany.
J Agric Food Chem. 2013 Oct 30;61(43):10293-301. doi: 10.1021/jf402448y. Epub 2013 Oct 18.
Worldwide, qualitative methods based on PCR are most commonly used as screening tools for genetically modified material in food and feed. However, the increasing number and diversity of genetically modified organisms (GMO) require effective methods for simultaneously detecting several genetic elements marking the presence of transgenic events. Herein we describe the development and validation of a pentaplex, as well as complementary triplex and duplex real-time PCR assays, for the detection of the most common screening elements found in commercialized GMOs: P-35S, T-nos, ctp2-cp4-epsps, bar, and pat. The use of these screening assays allows the coverage of many GMO events globally approved for commercialization. Each multiplex real-time PCR assay shows high specificity and sensitivity with an absolute limit of detection below 20 copies for the targeted sequences. We demonstrate by intra- and interlaboratory tests that the assays are robust as well as cost- and time-effective for GMO screening if applied in routine GMO analysis.
在全球范围内,基于聚合酶链式反应(PCR)的定性方法最常用于食品和饲料中转基因物质的筛选工具。然而,越来越多的转基因生物(GMO)的数量和多样性需要有效的方法来同时检测几个遗传标记,以确定转基因事件的存在。本文描述了一种五重实时 PCR 检测方法以及互补三重和双重实时 PCR 检测方法的开发和验证,用于检测商业化 GMO 中最常见的筛选元件:P-35S、T-nos、ctp2-cp4-epsps、bar 和 pat。这些筛选检测方法的使用可以涵盖许多全球批准商业化的 GMO 事件。每个多重实时 PCR 检测方法都具有高度的特异性和灵敏度,对于目标序列的绝对检测限低于 20 个拷贝。通过实验室内部和实验室之间的测试,我们证明如果在常规 GMO 分析中应用这些检测方法,它们具有稳健性,并且在成本和时间方面对于 GMO 筛选是有效的。