Matrix-normalised quantification of species by threshold-calibrated competitive real-time PCR: Allergenic peanut in food as one example

被引:16
作者
Holzhauser, Thomas [1 ]
Kleiner, Kornelia [1 ]
Janise, Annabella [1 ]
Roeder, Martin [1 ]
机构
[1] Paul Ehrlich Inst, Div Allergol, D-63225 Langen, Germany
关键词
PCR; ELISA; Quantitative; Species; Allergen; Threshold; Action level; POLYMERASE-CHAIN-REACTION; PROCESSED FOODS; INGREDIENTS; VALIDATION; ELISA; COOKIES;
D O I
10.1016/j.foodchem.2014.04.081
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel method to quantify species or DNA on the basis of a competitive quantitative real-time polymerase chain reaction (cqPCR) was developed. Potentially allergenic peanut in food served as one example. Based on an internal competitive DNA sequence for normalisation of DNA extraction and amplification, the cqPCR was threshold-calibrated against 100 mg/kg incurred peanut in milk chocolate. No external standards were necessary. The competitive molecule successfully served as calibrator for quantification, matrix normalisation, and inhibition control. Although designed for verification of a virtual threshold of 100 mg/kg, the method allowed quantification of 10-1000 mg/kg peanut incurred in various food matrices and without further matrix adaption: On the basis of four PCR replicates per sample, mean recovery of 10-1000 mg/kg peanut in chocolate, vanilla ice cream, cookie dough, cookie, and muesli was 87% (range: 39-147%) in comparison to 199% (range: 114-237%) by three commercial ELISA kits. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:68 / 76
页数:9
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