A PCR-microarray method for the screening of genetically modified organisms

被引:49
作者
Hamels, Sandrine [1 ]
Glouden, Thomas [1 ]
Gillard, Karine [1 ]
Mazzara, Marco [2 ]
Debode, Frederic [4 ]
Foti, Nicoletta [2 ]
Sneyers, Myriam [3 ]
Esteve Nuez, Teresa [5 ]
Pla, Maria [6 ]
Berben, Gilbert [4 ]
Moens, William [2 ]
Bertheau, Yves [7 ]
Audeon, Colette [7 ]
Van den Eede, Guy [2 ]
Remacle, Jose [1 ]
机构
[1] Eppendorf Array Technol SA, B-5000 Namur, Belgium
[2] Joint Res Ctr, Inst Hlth & Consumer Protect, European Commiss, I-21020 Ispra, VA, Italy
[3] Inst Sci Sante Publ ISP, SBB, B-1050 Brussels, Belgium
[4] Ctr Wallon Rech Agron CRA W, Dept Qualite Prod Agricoles, B-5030 Gembloux, Belgium
[5] IRTA, Consorcio CSIC, Barcelona 08034, Spain
[6] Univ Girona, Inst Tecnol Agroalimentaria INTEA, Girona 17071, Spain
[7] INRA, Lab Methodol Detect OGM, F-78026 Versailles, France
关键词
GMO; DNA microarray; PCR; Screening; DualChip GMO; Multiplex; EVENT-SPECIFIC DETECTION; DNA; QUANTIFICATION; MAIZE; IDENTIFICATION; FRAGMENTS; DIAGNOSIS; BT11;
D O I
10.1007/s00217-008-0960-5
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A new method to screen and to identify genetically modified organisms (GMO) is presented in this paper. It is based on the detection of multiple genetic elements common to GMO by their amplification via PCR followed by direct hybridisation of the amplicons on microarray. The pattern of the elements is then compared to a database of the composition of EU-approved GMO and an identification of the GMO is then proposed. The limit of detection of the method was a parts per thousand currency sign0.1% GMO content (w/w) expressed as the amount of target DNA present in the template for single unprocessed material. The DNA targets were detected both in reference materials and in mixtures with the same detection limit. The specificity for the detection of the different elements was found to be very good with no cross-reaction even in samples with two GMO present at different concentrations. The paper presents examples of GMO identification and discusses the potential and limitation of such approaches and how they can facilitate the work of private and enforcement detection laboratories.
引用
收藏
页码:531 / 541
页数:11
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