A practical approach to screen for authorised and unauthorised genetically modified plants

In routine analysis, screening methods based on real-time PCR are most commonly used for the detection of genetically modified (GM) plant material in food and feed. In this paper, it is shown that the combination of five DNA target sequences can be used as a universal screening approach for at least 81 GM plant events authorised or unauthorised for placing on the market and described in publicly available databases. Except for maize event LY038, soybean events DP-305423 and BPS-CV127-9 and cotton event 281-24-236 × 3006-210-23, at least one of the five genetic elements has been inserted in these GM plants and is targeted by this screening approach. For the detection of these sequences, fully validated real-time PCR methods have been selected. A screening table is presented that describes the presence or absence of the target sequences for most of the listed GM plants. These data have been verified either theoretically according to available databases or experimentally using available reference materials. The screening table will be updated regularly by a network of German enforcement laboratories.

[1]  A. Schroeder,et al.  Die Untersuchung von transgenem Rapspollen in Honigen mittels Real-time-PCR , 2005 .

[2]  Arne Holst-Jensen,et al.  PCR technology for screening and quantification of genetically modified organisms (GMOs) , 2003, Analytical and bioanalytical chemistry.

[3]  M. Feinberg,et al.  Quantitation of 35S promoter in maize DNA extracts from genetically modified organisms using real-time polymerase chain reaction, part 2: interlaboratory study. , 2005, Journal of AOAC International.

[4]  Hans-Ulrich Waiblinger,et al.  Collaborative trial validation studies of real-time PCR-based GMO screening methods for detection of the bar gene and the ctp2-cp4epsps construct. , 2009, Journal of agricultural and food chemistry.

[5]  Rodriguez Cerezo Emilio,et al.  The global pipeline of new GM crops: implications of asynchronous approval for international trade , 2009 .

[6]  Y. Bertheau,et al.  An accurate real-time PCR test for the detection and quantification of cauliflower mosaïc virus (CaMV): applicable in GMO screening , 2008 .

[7]  H. Broll,et al.  Collaborative Study of a T-nos Real-Time PCR Method for Screening of Genetically Modified Organisms in Food Products , 2007, Journal für Verbraucherschutz und Lebensmittelsicherheit.

[8]  H. Waiblinger,et al.  Validation and collaborative study of a P35S and T-nos duplex real-time PCR screening method to detect genetically modified organisms in food products , 2008 .

[9]  E. D. Earle,et al.  Nuclear DNA content of some important plant species , 2007, Plant Molecular Biology Reporter.

[10]  Yves Bertheau,et al.  Validation of the performance of a GMO multiplex screening assay based on microarray detection , 2008 .

[11]  J. Mano,et al.  Real-time PCR array as a universal platform for the detection of genetically modified crops and its application in identifying unapproved genetically modified crops in Japan. , 2009, Journal of agricultural and food chemistry.