A group-specific, quantitative real-time PCR assay for detection of crab, a crustacean shellfish allergen, in complex food matrices

被引:26
作者
Eischeid, Anne C. [1 ]
Stadig, Sarah R. [1 ]
机构
[1] US FDA, Ctr Food Safety & Appl Nutr, Off Regulatory Sci, 5100 Paint Branch Pkwy, College Pk, MD 20740 USA
关键词
Crab; Crustacean; qPCR; Real-time PCR; Allergen; Mitochondria; 12S rRNA gene; Internal amplification control; DNA; PRESSURE;
D O I
10.1016/j.foodchem.2017.10.045
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A real-time PCR assay was developed for detection of crab, a crustacean allergen, in food products. Group-specific primers and probes were developed to detect numerous species of crab. Method validation included tests of detection in complex food matrices, evaluation of commercial food products, and cross-reactivity testing on a wide variety of crustaceans. The method was able to detect several species of crab spiked into complex food matrices at levels ranging from 0.1 to 10(5) parts per million (weight/weight), worked equally well on different platforms, exhibited high specificity for crab over other types of crustaceans, and yielded much higher signals from commercial food products listing crab as an ingredient than from those containing other crustaceans.
引用
收藏
页码:224 / 231
页数:8
相关论文
共 16 条
  • [1] Adams P.S., 2006, Real-time PCR, P39
  • [2] Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques
    Aljanabi, SM
    Martinez, I
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (22) : 4692 - 4693
  • [3] The effect of processing parameters on DNA degradation in food
    Bauer, T
    Weller, P
    Hammes, WP
    Hertel, C
    [J]. EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2003, 217 (04) : 338 - 343
  • [4] Combined Effects of Temperature, Pressure and Low pH on the Amplification of DNA of Plant Derived Foods
    Bergerova, Eva
    Godalova, Zuzana
    Siekel, Peter
    [J]. CZECH JOURNAL OF FOOD SCIENCES, 2011, 29 (04) : 337 - 345
  • [5] A versatile internal control for use as DNA in real-time PCR and as RNA in real-time reverse transcription PCR assays
    Deer, D. M.
    Lampel, K. A.
    Gonzalez-Escalona, N.
    [J]. LETTERS IN APPLIED MICROBIOLOGY, 2010, 50 (04) : 366 - 372
  • [6] Optimization and evaluation of a method for the generation of DNA barcodes for the identification of crustaceans
    Eischeid, Anne C.
    Stadig, Sarah R.
    Handy, Sara M.
    Fry, Frederick S.
    Deeds, Jonathan
    [J]. LWT-FOOD SCIENCE AND TECHNOLOGY, 2016, 73 : 357 - 367
  • [7] Development and evaluation of a real-time PCR assay for detection of lobster, a crustacean shellfish allergen
    Eischeid, Anne C.
    [J]. FOOD CONTROL, 2016, 59 : 393 - 399
  • [8] Two Quantitative Real-Time PCR Assays for the Detection of Penaeid Shrimp and Blue Crab, Crustacean Shellfish Allergens
    Eischeid, Anne C.
    Kim, Bang-hyun
    Kasko, Sasha M.
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2013, 61 (24) : 5669 - 5674
  • [9] ENGL-European Network of GMO Laboratories, 2015, JRC TECHNICAL REPORT
  • [10] Effect of heat and pressure processing on DNA fragmentation and implications for the detection of meat using a real-time polymerase chain reaction
    Hird, H
    Chisholm, J
    Sanchez, A
    Hernandez, M
    Goodier, R
    Schneede, K
    Boltz, C
    Popping, B
    [J]. FOOD ADDITIVES AND CONTAMINANTS, 2006, 23 (07): : 645 - 650