Qualitative and Quantitative Analysis of Canine (Canis lupus familiaris) Meat in Meatballs for Halal Authentication Study using Real-time Polymerase Chain Reaction

被引:4
|
作者
Kurniasih, Kholif Sholehah, I [1 ]
Hikmah, Nurull [1 ]
Erwanto, Yuny [2 ,3 ]
Rohman, Abdul [1 ,3 ]
机构
[1] Gadjah Mada Univ, Dept Pharmaceut Chem, Sekip Utara 55281, Yogyakarta, Indonesia
[2] Gadjah Mada Univ, Fac Anim Sci, Div Anim Prod Technol, Jl Fauna 3, Bulaksumur 55281, Yogyakarta, Indonesia
[3] Gadjah Mada Univ, IHIS, Sekip Utara 55281, Yogyakarta, Indonesia
关键词
Canine meat; Real-time PCR; Species-specific primer; Halal authentication; Meatballs; MULTIPLEX PCR ASSAY; CYTOCHROME-B GENE; WILD BOAR MEAT; SPECIES IDENTIFICATION; DOG MEAT; BEEF MEATBALL; ADULTERATION; SPECTROSCOPY; FOODS;
D O I
10.17957/IJAB/15.1264
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Canine meat (CM), one of non-halal meats having low price value, may be used as substitute or meat adulterant in beef meatballs by unethical producers to get economic benefits. This study was intended to design and to validate specific primer targeting on cytochrome-b gene for detection of CM in meatballs using real-time polymerase chain reaction (real-time PCR). The primer was in silico designed and was subjected to specificity test against DNAs extracted from several meats. The evaluation of other validation parameters for quantitative analysis was also performed including linearity, efficiency, sensitivity, repeatability and its application to commercial samples. The designed primer (CYTBCA3-kh) consisted of F: CCT TAG CCA ATG CCT ATT C and R: GCG ACT TGT CCG ATA ATG. The results showed that CYTBCA3-kh primer was specific to DNA extracted from CM and that extracted from meatballs containing CM using optimized annealing temperature of 50.6 degrees C. The detection limit reported was 50 pg DNA corresponding to 0.1% CM in meatballs containing CM and beef. The relative standard deviation (RSD) for precision assay met the required acceptance criteria. The validated real-time PCR using CYTBCA3-kh primer could successfully identify CM in meatball formulation for halal authentication analysis. The developed method was potential to be developed as official standard method for CM detection in meatball products. (C) 2020 Friends Science Publishers
引用
收藏
页码:103 / 108
页数:6
相关论文
共 50 条
  • [31] Real-Time Quantitative Polymerase Chain Reaction Analysis of Patients With Refractory Chronic Periodontitis
    Marconcini, Simone
    Covani, Ugo
    Barone, Antonio
    Vittorio, Orazio
    Curcio, Michele
    Barbuti, Serena
    Scatena, Fabrizio
    Felli, Lamberto
    Nicolini, Claudio
    JOURNAL OF PERIODONTOLOGY, 2011, 82 (07) : 1018 - 1024
  • [32] Immunopolymerase chain reaction using real-time polymerase chain reaction for detection
    Sims, PW
    Vasser, M
    Wong, WL
    Williams, PM
    Meng, YG
    ANALYTICAL BIOCHEMISTRY, 2000, 281 (02) : 230 - 232
  • [33] Real-time quantitative polymerase chain reaction to assess gene transfer
    Becker, K
    Pan, D
    Whitley, CB
    HUMAN GENE THERAPY, 1999, 10 (15) : 2559 - 2566
  • [34] New buffers to improve the quantitative real-time polymerase chain reaction
    Ahmad, Ashraf
    Ghasemi, Jahan
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2007, 71 (08) : 1970 - 1978
  • [35] New Developments in Quantitative Real-time Polymerase Chain Reaction Technology
    Gadkar, Vijay J.
    Filion, Martin
    CURRENT ISSUES IN MOLECULAR BIOLOGY, 2014, 16 : 1 - 5
  • [36] Conventional multiplex polymerase chain reaction (PCR) versus real-time PCR for species-specific meat authentication
    Edris, S.
    Mutwakil, M. H. Z.
    Abuzinadah, O. A.
    Mohammed, H. E.
    Ramadan, A.
    Gadalla, N. O.
    Shokry, A. M.
    Hassan, S. M.
    Shoaib, R. M.
    El-Domyati, F. M.
    Bahieldin, A.
    LIFE SCIENCE JOURNAL-ACTA ZHENGZHOU UNIVERSITY OVERSEAS EDITION, 2012, 9 (04): : 5831 - 5837
  • [37] Detection of peanut using real-time polymerase chain reaction
    H. Hird
    J. Lloyd
    R. Goodier
    J. Brown
    P. Reece
    European Food Research and Technology, 2005, 220 : 238 - 238
  • [38] Rapid detection of trisomy 21 by gene dosage analysis using quantitative real-time polymerase chain reaction
    Tsujie, Tomoko
    Takemura, Masahiko
    Kimura, Tadashi
    Shimoya, Koichiro
    Tsutsui, Tateki
    Ogita, Kazuhide
    Ozaki, Mamoru
    Murata, Yuji
    JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2006, 32 (04) : 368 - 372
  • [39] Detection of peanut using real-time polymerase chain reaction
    H. Hird
    J. Lloyd
    R. Goodier
    J. Brown
    P. Reece
    European Food Research and Technology, 2003, 217 : 265 - 268
  • [40] Detection of peanut using real-time polymerase chain reaction
    Hird, H
    Lloyd, J
    Goodier, R
    Brown, J
    Reece, P
    EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 2003, 217 (03) : 265 - 268