Droplet digital PCR (ddPCR) method for the detection and quantification of goat and sheep derivatives in commercial meat products

被引:33
作者
Wang, Qiang [1 ]
Cai, Yicun [1 ]
He, Yuping [1 ]
Yang, Litao [2 ]
Li, Jian [1 ]
Pan, Liangwen [1 ]
机构
[1] Shanghai Entry Exit Inspect & Quarantine Bur Chin, Tech Ctr Anim Plant & Food Inspect & Quarantine, Pudong New Area, 1208 Minsheng Rd, Shanghai 200135, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Minhang Area, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
基金
中国博士后科学基金;
关键词
Droplet digital PCR; Quantification; Nuclear DNA; Plasmid; Meat product; REAL-TIME PCR; DNA COPY NUMBER; ABSOLUTE QUANTIFICATION; PORCINE MATERIALS; FOOD-CHAIN; IDENTIFICATION; ASSAY; VALIDATION; BUFFALO; ADULTERATION;
D O I
10.1007/s00217-017-3000-5
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A highly precise, quantitative method based on the droplet digital polymerase chain reaction (ddPCR) technique was developed to identify and quantify the goat and sheep content in meat products. A formula for calculating raw meat weight based on DNA copy number was established. Exclusive specificity was verified using samples from 24 different animal species, and inclusive specificity between goat and sheep was tested using five different breeds for each species. The limit of detection and the limit of quantitation for both goat and sheep were 1 and 5 copies/mu L, respectively, using a cloned plasmid containing goat- and sheep-specific target DNA fragments as calibrators. The accuracy and applicability of the method were verified using mixed powder samples with known proportions of goat and sheep meat, simulate meatball samples, and commercially available products, respectively. The results confirmed that the developed ddPCR methods are highly precise for identifying and quantifying the goat and sheep meat, indicating their potential applicability in future routine analyses.
引用
收藏
页码:767 / 774
页数:8
相关论文
共 36 条
  • [1] Species determination - Can we detect and quantify meat adulteration?
    Ballin, Nicolai Z.
    Vogensen, Finn K.
    Karlsson, Anders H.
    [J]. MEAT SCIENCE, 2009, 83 (02) : 165 - 174
  • [2] Long and short forms of the ovine prolactin receptor: cDNA cloning and genomic analysis reveal that the two forms arise by different alternative splicing mechanisms in ruminants and in rodents
    Bignon, C
    Binart, N
    Ormandy, C
    Schuler, LA
    Kelly, PA
    Djiane, J
    [J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1997, 19 (02) : 109 - 120
  • [3] Boehler P, 2013, POISONING MAY POINT
  • [4] Interlaboratory validation of a real-time PCR detection method for bovine and ovine-derived material
    Cai, Yicun
    Wang, Qiang
    He, Yuping
    Pan, Liangwen
    [J]. MEAT SCIENCE, 2017, 134 : 119 - 123
  • [5] Detection and quantification of beef and pork materials in meat products by duplex droplet digital PCR
    Cai, Yicun
    He, Yuping
    Lv, Rong
    Chen, Hongchao
    Wang, Qiang
    Pan, Liangwen
    [J]. PLOS ONE, 2017, 12 (08):
  • [6] Quantitative Analysis of Pork and Chicken Products by Droplet Digital PCR
    Cai, Yicun
    Li, Xiang
    Lv, Rong
    Yang, Jielin
    Li, Jian
    He, Yuping
    Pan, Liangwen
    [J]. BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [7] Tolerance of Droplet-Digital PCR vs Real-Time Quantitative PCR to Inhibitory Substances
    Dingle, Tanis C.
    Sedlak, Ruth Hall
    Cook, Linda
    Jerome, Keith R.
    [J]. CLINICAL CHEMISTRY, 2013, 59 (11) : 1670 - 1672
  • [8] Development and validation of a TaqMan real-time PCR assay for the identification and quantification of roe deer (Capreolus capreolus) in food to detect food adulteration
    Druml, Barbara
    Mayer, Walter
    Cichna-Markl, Margit
    Hochegger, Rupert
    [J]. FOOD CHEMISTRY, 2015, 178 : 319 - 326
  • [9] [范丽丽 Fan Lili], 2014, [食品科学, Food Science], V35, P248
  • [10] Detection of adulterated murine components in meat products by TaqMan© real-time PCR
    Fang, Xin
    Zhang, Chi
    [J]. FOOD CHEMISTRY, 2016, 192 : 485 - 490