Inter-laboratory validation by event-specific qPCR methods for the detection of genetically modified insect and herbicide-tolerant maize DBN9501

被引:0
作者
Wang, Jing [1 ]
Xiao, Bing [2 ,3 ]
Zhang, Ruiying [1 ]
Guan, Haitao [1 ]
Yang, Yang [1 ]
Ding, Yijia [1 ]
Yuan, Ran [1 ]
Zhang, Xiaolei [1 ]
Li, Lingyan [4 ]
Liang, Jingang [5 ]
Wen, Hongtao [1 ]
机构
[1] Heilongjiang Acad Agr Sci, Qual & Safety Inst Agr Prod, Harbin 150086, Peoples R China
[2] Chinese Acad Agr Sci, Inst Agr Resources & Reg Planning, Beijing 100081, Peoples R China
[3] China Agr Univ, Coll Resources & Environm Sci, Beijing 100091, Peoples R China
[4] Beijing Vocat Coll Agr, Beijing 102442, Peoples R China
[5] Minist Agr & Rural Affairs Peoples Republ China, Dev Ctr Sci & Technol, Beijing 100176, Peoples R China
关键词
Genetically modified maize; DBN9501; GMO; Event-specific method; Inter-laboratory ring trial; RT-PCR; CHAIN-REACTION METHODS; PCR DETECTION METHODS; MODIFIED ORGANISMS;
D O I
10.1007/s00003-023-01450-z
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
DBN9501 is a new maize transgenic event characterised by being resistance to insects and herbicides. To meet genetically modified (GM)-labeling requirements and monitor the unintended release of genetically modified organisms (GMOs), developing a creditable and applicable method for identifying and quantifying GM events is essential. Herein we developed an event-specific method and validated it through inter-laboratory ring trials using blind samples. The limit of detection (LOD) and limit of quantification (LOQ) of copy number ratio were confirmed at 0.05% and 0.1%, respectively. The quantitative bias ranged from -3.52 to 10.38%, and the relative standard deviation (RSD) of the method was < 25%. Furthermore, the expanded uncertainty for the blind samples S1 - S5 was 0.22%, 0.10%, 0.05%, 0.03%, and 0.02%. These results demonstrated that the event-specific quantitative PCR method could identify and quantify GM DBN9501 for further routine lab analysis.
引用
收藏
页码:451 / 460
页数:10
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