リアルタイムPCR を用いた遺伝子組換えダイズにおける 定性PCR 法と定量PCR 法の相関性の検証

The Notice of the Deputy Commissioner of the Consumer Affairs Agency dated 15th September 2021 (No. 389) regarding “Partial Amendments to ‘Food Labeling Standards’” (24th amendment), which is a notice amending the Notice of the Deputy Commissioner of the Consumer Affairs Agency dated 30th March 2015 (No. 139) regarding “Food Labeling Standards”, added a new inspection method for soybean grains (to determine contamination with genetically modified agricultural products) to the “Attachment: Inspection methods for genetically modified foods that have been safety reviewed.” We verified the correlation between qualitative PCR analysis using the ΔΔCq method and quantitative PCR assessment that has been traditionally used as the test method for determining appropriateness of food labeling of identity preserved handling. Qualitative PCR was performed on six soybean samples (samples 2–7) collected in 2021 from businesses in Mie Prefecture that import from countries outside Japan and one sample of domestically produced soybeans (sample 1) that was labelled as non-genetically modified; additionally, the RRS, LLS, and RR2 contamination rates were known for samples 2-7, which had passed quantitative PCR testing before qualitative PCR was performed. In these samples, quantitative PCR result for sample 7 showed that RRS, LLS, and RR2 contents were 0.02%, 0.00%, and 0.13%, respectively. Quantitative PCR result for sample 4 showed that RRS, LLS, and RR2 contents were 0.00%, 0.00%, and 0.04%, respectively. In qualitative PCR, sample 7 was assessed as positive, whereas sample 4 was assessed as negative. These results suggest that the likelihood of a positive result in qualitative PCR increases when the RR2 content alone exceeds 0.13%. Moreover, the qualitative PCR result may be positive even if the quantitative PCR result is below the limit of quantification (0.3%).