Bird Patrick, Benzinger M Joseph, Bastin Benjamin, Crowley Erin, Agin James, Goins David, Clark Mike, Tourniaire Jean-Philippe, Pierre Sophie, Lauer Wendy
Q Laboratories, Inc., 1400 Harrison Ave, Cincinnati, OH 45214, USA.
Bio-Rad, 2000 Alfred Nobel Dr., Hercules, CA 94547, USA.
J AOAC Int. 2018 Jul 1;101(4):1043-1057. doi: 10.5740/jaoacint.17-0426. Epub 2018 Apr 4.
The iQ-Check Salmonella II Real-Time PCR test kit utilizes Salmonella-specific oligonucleotide probes and primers for the rapid and specific detection of Salmonella species in select food types. The alternative method was evaluated by using 375 g test portions in an unpaired study design for two matrices, milk chocolate and dry dog food. Each matrix was compared with the U.S. Food and Drug Administration Chapter 5 Salmonella reference method. Fourteen technicians from 12 laboratories, including academia and industry, located within the United States and Canada participated in the collaborative study. Three levels of contamination were evaluated for each matrix: an uninoculated control level (0 CFU/test portion), a low inoculum level (0.2-2 CFU/test portion), and a high inoculum level (2-5 CFU/test portion). The statistical analysis was conducted according to the Probability of Detection (POD) statistical model. The results obtained for the low inoculum level test portions produced a difference in the candidate presumptive and confirmatory results (dLPOD) value with a 95% confidence interval of -0.05, (-0.15, 0.06) for the milk chocolate and 0.10, (-0.01, 0.21) for the dry dog food. The dLPOD results indicate an equivalence between the candidate method and reference method for the matrices evaluated, and the method demonstrated acceptable interlaboratory reproducibility as determined in the collaborative evaluation. False positive and false negative rates were determined for each matrix and produce values of <2%. Based on the data generated, the method demonstrated acceptable interlaboratory reproducibility data and statistical analysis.
iQ-Check沙门氏菌II实时荧光定量PCR检测试剂盒利用沙门氏菌特异性寡核苷酸探针和引物,用于快速、特异性地检测特定食品类型中的沙门氏菌。在一项针对两种基质(牛奶巧克力和干狗粮)的非配对研究设计中,使用375克测试份对替代方法进行了评估。每种基质都与美国食品药品监督管理局第5章沙门氏菌参考方法进行了比较。来自美国和加拿大的12个实验室(包括学术界和工业界)的14名技术人员参与了这项协作研究。对每种基质评估了三个污染水平:未接种对照水平(0 CFU/测试份)、低接种水平(0.2 - 2 CFU/测试份)和高接种水平(2 - 5 CFU/测试份)。根据检测概率(POD)统计模型进行统计分析。低接种水平测试份的结果显示,牛奶巧克力的候选推定和确证结果的差异(dLPOD)值的95%置信区间为 -0.05,(-0.15, 0.06),干狗粮为0.10,(-0.01, 0.21)。dLPOD结果表明,对于所评估的基质,候选方法与参考方法等效,并且该方法在协作评估中显示出可接受的实验室间重现性。确定了每种基质的假阳性和假阴性率,其值均<2%。基于所生成的数据,该方法显示出可接受的实验室间重现性数据和统计分析结果。