Development of a new qPCR method for specific detection and quantification of genetically modified maize MON863. (August 2018)

• Record Type: Journal Article
• Authors: Guertler, Patrick; Pecoraro, Sven; Naumann, Heike; Busch, Ulrich
• Is Part Of: Food control. Volume 90(2018)
• Page Start: 466
• Page End: 471
• Publication Date: 2018-08
• Subjects: Maize -- GMO -- MON863 -- qPCR -- DNA Sanger sequencing -- In-house method validation; Food -- Quality -- Periodicals; Food -- Analysis -- Periodicals; Food handling -- Periodicals; Food industry and trade -- Quality control -- Periodicals; Aliments -- Industrie et commerce -- Qualité -- Contrôle -- Périodiques; Aliments -- Qualité -- Périodiques; Aliments -- Analyse -- Périodiques; Hygiène alimentaire -- Périodiques; Food -- Analysis; Food handling; Food -- Quality; Periodicals; Electronic journals; 664.07
• DOI: 10.1016/j.foodcont.2018.03.021
• Languages: English
• ISSNs: 0956-7135

Abstract

Abstract: Analysis of non-transgenic seed samples for the presence of genetically modified maize MON863 revealed unexpected amplification signals using an official qPCR method. These amplification signals only occured when using other master mix products as in the original validation process. DNA sequence data from an unspecific amplicon could be mapped to mitochondrial maize DNA reference sequence. Oligo sequence analysis revealed that forward primer and probe both can hybridize to the mitochondrial maize DNA leading to unspecific amplification signals in qPCR. Therefore, we designed and validated a new qPCR method for event MON863 with a LOD of 5 copies per reaction. The method shows high specificity as no unspecific amplification signal was detected after analysis of reference material for different genetically modified crops and conventional maize samples. Robustness tests were performed in two different laboratories and no effects on method performance could be observed when using different master mixes and qPCR devices, as well as with variation in oligonucleotide concentrations. Highlights: Unspecific amplification when using the official MON863 qPCR detection method. Unspecific amplicon can be mapped to maize mitochondrial DNA. Development & in-house validation of a new detection method for MON863. Newly developed detection method for MON863 is highly specific. Method meets the minimum performance requirements for analytical methods (ENGL).