Inter-laboratory analysis of selected genetically modified plant reference materials with digital PCR

被引:11
作者
Dobnik, David [1 ]
Demsar, Tina [1 ]
Huber, Ingrid [2 ]
Gerdes, Lars [2 ]
Broeders, Sylvia [3 ]
Roosens, Nancy [3 ]
Debode, Frederic [4 ]
Berben, Gilbert [4 ]
Zel, Jana [1 ]
机构
[1] Natl Inst Biol NIB, Dept Biotechnol & Syst Biol, Vecna Pot 111, Ljubljana 1000, Slovenia
[2] Bavarian Hlth & Food Safety Author LGL, Vet Str 2, D-85764 Oberschleissheim, Germany
[3] Sci Inst Publ Hlth WIV ISP, J Wytsmanstr 14, B-1050 Brussels, Belgium
[4] Walloon Agr Res Ctr CRA W, Chaussee Namur 24, B-5030 Gembloux, Belgium
关键词
Digital PCR; Droplet digital PCR; Absolute quantification; Reference materials; GMO quantification; POLYMERASE-CHAIN-REACTION; MULTIPLEX QUANTIFICATION; MODIFIED ORGANISMS; GMO DETECTION; DNA; LECTIN;
D O I
10.1007/s00216-017-0711-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Digital PCR (dPCR), as a new technology in the field of genetically modified (GM) organism (GMO) testing, enables determination of absolute target copy numbers. The purpose of our study was to test the transferability of methods designed for quantitative PCR (qPCR) to dPCR and to carry out an inter-laboratory comparison of the performance of two different dPCR platforms when determining the absolute GM copy numbers and GM copy number ratio in reference materials certified for GM content in mass fraction. Overall results in terms of measured GM% were within acceptable variation limits for both tested dPCR systems. However, the determined absolute copy numbers for individual genes or events showed higher variability between laboratories in one third of the cases, most possibly due to variability in the technical work, droplet size variability, and analysis of the raw data. GMO quantification with dPCR and qPCR was comparable. As methods originally designed for qPCR performed well in dPCR systems, already validated qPCR assays can most generally be used for dPCR technology with the purpose of GMO detection.
引用
收藏
页码:211 / 221
页数:11
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