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Development and assessment of a duplex droplet digital PCR method for quantification of GM rice Kemingdao

文献类型： 外文期刊

作者： Li, Jun 1 ; Zhai, Shanshan 1 ; Gao, Hongfei 1 ; Xiao, Fang 1 ; Li, Yunjing 1 ; Wu, Gang 1 ; Wu, Yuhua 1 ;

作者机构： 1.Chinese Acad Agr Sci, Oil Crops Res Inst, Key Lab Biol & Genet Improvement Oil Crops, Minist Agr & Rural Affairs, Wuhan 430062, Hubei, Peoples R China

关键词： Genetically modified organisms; Kemingdao; Droplet digital PCR; Real-time quantitative PCR; GMO quantification; Comparison

期刊名称：ANALYTICAL AND BIOANALYTICAL CHEMISTRY （ 影响因子：3.637； 五年影响因子：3.444 ）

ISSN： 1618-2642

年卷期：

页码：

收录情况： SCI

摘要： The implementation of genetically modified organism (GMO) labeling policies requires accurate quantitative methods to measure the GMO content in test samples. A Kemingdao/phospholipase D (KMD/PLD) duplex ddPCR method was established with rice genomic DNA (gDNA) of homozygous KMD as template by optimizing the annealing temperature and cycle number. Duplex ddPCR showed a linear response over the dynamic range from 68 to 175,000 copies, covering four orders of magnitude. The limit of detection (LOD) and limit of quantification (LOQ) for duplex ddPCR were determined to be 9 copies and 34 copies of the rice haploid genome, respectively. A very high dilution factor would result in unacceptable bias and coefficients of variation for determining copy number of the gDNA solution, and more than 1000 copies of the DNA template in one reaction is preferred to obtain accurate quantitative results by duplex PCR. Five blinded DNA samples with copy number ratio of 10%, 5%, 1%, 0.1%, and 0.05%, and three blinded real-life matrix samples with mass fraction of 5%, 1%, and 0.5% were quantified by duplex ddPCR, simplex ddPCR, and qPCR. These three methods all gave comparable GMO content and copy numbers within the required precision, but the duplex ddPCR showed the narrowest uncertainty interval and provided the highest precision in comparison to simplex ddPCR and qPCR. The ddPCR is a more appealing and reliable technology for the accurate quantification of GMO content than simplex ddPCR and qPCR considering the uncertainty and precision of quantitative results, the time consumption of generating droplets, and the cost of ddPCR reagents.

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