Ring trial validation of single and multiplex real-time PCR methods for the detection and quantification of the allergenic food ingredients sesame, almond, lupine and Brazil nut

被引:19
|
作者
Waiblinger, Hans-Ulrich [1 ]
Boernsen, Britta [1 ]
Naeumann, Gabriele [2 ]
Koeppel, Ren [3 ]
机构
[1] Chem & Veterinaruntersuchungsamt Freiburg, D-79114 Freiburg, Germany
[2] Inst Hyg & Umwelt IHU, D-20539 Hamburg, Germany
[3] Kanton Lab Zurich, CH-8032 Zurich, Switzerland
关键词
Allergen; Sesame; Almond; Lupine; Brazil nut; Real time PCR; Interlaboratory validation; Quantification; MUSTARD SINAPIS-ALBA; DNA;
D O I
10.1007/s00003-014-0868-x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The inter-laboratory (=ring-trial) validation of 4 food allergen quantification methods using real-time PCR is described. Three single real-time PCR methods for the specific detection and quantification of sesame, almond and Brazil nut were used. Additionally, a multiplex real-time PCR method combining the detection of sesame, almond, Brazil nut and lupine was tested in parallel. Matrix based calibrants (rice cookies) spiked (=incurred) with defined amounts of sesame, almond, lupine and Brazil nut were applied for quantitative evaluation. Cookies based upon wheat and rice flour as well as sauce hollandaise powder each incurred with these allergenic ingredients in the range of 10-123 milligram per kilogram were used as ring-trial samples. The lowest spike level of 10 mg/kg could reproducibly be detected by 6 of 7 PCR systems. In quantitative evaluation of the results, reproducibility standard deviations of approximately 50 % and below were obtained. In addition, the effect of the food matrix on allergen quantification was examined. The range of "recoveries" over all matrices and methods was from 43 to 109 %.
引用
收藏
页码:297 / 310
页数:14
相关论文
共 36 条
  • [31] Real-Time PCR Assay for the Detection and Quantification of Roe Deer to Detect Food Adulteration-Interlaboratory Validation Involving Laboratories in Austria, Germany, and Switzerland
    Druml, Barbara
    Uhlig, Steffen
    Simon, Kirsten
    Frost, Kirstin
    Hettwer, Karina
    Cichna-Markl, Margit
    Hochegger, Rupert
    FOODS, 2021, 10 (11)
  • [32] Validation of a single tube quantitative real-time RT-PCR (QRT-PCR) assay for the detection and quantification of the BCR-ABL minor breakpoint in acute lymphoblastic leukemia (ALL).
    Siddiqui, R
    Dumur, CI
    Ladd, AC
    Wilkinson, DS
    Carleton, GT
    Ferreira-Gonzalez, A
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2005, 7 (05): : 662 - 662
  • [33] Collaborative Trial Validation Studies of Real-Time PCR-Based GMO Screening Methods for Detection of the bar Gene and the ctp2-cp4epsps Construct
    Grohmann, Lutz
    Bruenen-Nieweler, Claudia
    Nemeth, Anne
    Waiblinger, Hans-Ulrich
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2009, 57 (19) : 8913 - 8920
  • [34] Development, Optimization, and Single Laboratory Validation of an Event-Specific Real-Time PCR Method for the Detection and Quantification of Golden Rice 2 Using a Novel Taxon-Specific Assay
    Jacchia, Sara
    Nardini, Elena
    Savini, Christian
    Petrillo, Mauro
    Angers-Loustau, Alexandre
    Shim, Jung-Hyun
    Trijatmiko, Kurniawan
    Kreysa, Joachim
    Mazzara, Marco
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2015, 63 (06) : 1711 - 1721
  • [35] Towards an international standard for detection and typing botulinum neurotoxin-producing Clostridia types A, B, E and F in food, feed and environmental samples: A European ring trial study to evaluate a real-time PCR assay
    Fenicia, Lucia
    Fach, Patrick
    van Rotterdam, Bart J.
    Anniballi, Fabrizio
    Segerman, Bo
    Auricchio, Bruna
    Delibato, Elisabetta
    Hamidjaja, Raditijo A.
    Wielinga, Peter R.
    Woudstra, Cedric
    Agren, Joakim
    De Medici, Dario
    Knutsson, Rickard
    INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2011, 145 : S152 - S157
  • [36] A new single-tube platform of melting temperature curve analysis based on multiplex real-time PCR using EvaGreen for simultaneous screening detection of Shiga toxin-producing Escherichia coli, Salmonella spp. and Listeria monocytogenes in food
    Bundidamorn, Damkerng
    Supawasit, Wannakarn
    Trevanich, Sudsai
    FOOD CONTROL, 2018, 94 : 195 - 204