Establishment of conventional PCR and real-time PCR assays for accurate, rapid and quantitative authentication of four mistletoe species

被引:7
|
作者
Kim, Wook Jin [1 ]
Yang, Sungyu [1 ]
Choi, Goya [1 ]
Park, Inkyu [1 ]
Noh, Pureum [1 ]
Lee, A. Yeong [1 ]
Kim, Hyo Seon [1 ]
Moon, Byeong Cheol [1 ]
机构
[1] Korea Inst Oriental Med, Herbal Med Resources Res Ctr, 111 Geonjae Ro, Naju 58245, Jeollanam Do, South Korea
关键词
Viscum coloratura; Santalaceae; Genetic analysis; Maturase K; DNA; IDENTIFICATION; VALIDATION; SCAR; FOODS; RAW;
D O I
10.1016/j.phytochem.2020.112400
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adulterants in processed food and herbal medicines reduce their safety, quality control, or pharmacological efficacy. Four mistletoe species, including Viscum coloratum, inhabit Korea. Leaves and branches of V. coloratum, defined as edible or medicinal mistletoe species in Korean, are used to prepare Korean herbal medicines as well as leached tea. However, other mistletoe species including Taxillus sutchuenensis var. duclouxii, Korthalsella japonica, and Loranthus tanakae are frequently distributed as authentic V. coloratum in Korean markets because of similarities in the branches morphology and Korean names of these species with V. coloratum. Although herbal medicines and food products prepared from the other mistletoe species are inauthentic, they are sold at high prices because of the rarity of these species. Thus, it is important to distinguish between authentic and inauthentic adulterant mistletoe species. In this study, we developed species-specific primer, based on matK sequences, suitable for both conventional PCR and real time PCR (qPCR) assay. These assays allowed rapid discrimination among all four mistletoe species. Moreover, qPCR assay enabled the detection of trace amounts of adulterant mistletoe species in V. coloratum samples. Furthermore, we used these assays to monitor commercial mistletoe products distributed in Korean markets. Our data suggest that these methods would serve as a reliable genetic tool to prevent adulteration and standardize the quality of commercial V. coloratum products.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Comparison of conventional, nested, and real-time PCR assays for rapid and accurate detection of Vibrio vulnificus
    Kim, Hyong Sun
    Kim, Dong-Min
    Neupane, Ganesh Prasad
    Lee, Yu-mi
    Yang, Nam-Woong
    Jang, Sook Jin
    Jung, Sook-In
    Park, Kyung-Hwa
    Park, Hae-Ryoung
    Lee, Chang Seop
    Lee, Sun Hee
    JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (09) : 2992 - 2998
  • [2] TaqMan real-time PCR versus four conventional PCR assays for detection of apple proliferation phytoplasma
    S. Baric
    C. Kerschbamer
    J. Dalla Via
    Plant Molecular Biology Reporter, 2006, 24
  • [3] TaqMan real-time PCR versus four conventional PCR assays for detection of apple proliferation phytoplasma
    Baric, S.
    Kerschbamer, C.
    Dalla Via, J.
    PLANT MOLECULAR BIOLOGY REPORTER, 2006, 24 (02) : 169 - 184
  • [4] Development of Conventional and Real-Time Quantitative PCR Assays for Diagnosis and Monitoring of Scabies
    Wong, Samson S. Y.
    Poon, Rosana W. S.
    Chau, Sandy
    Wong, Sally C. Y.
    To, Kelvin K. W.
    Cheng, Vincent C. C.
    Fung, Kitty S. C.
    Yuen, K. Y.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2015, 53 (07) : 2095 - 2102
  • [5] Conventional versus real-time quantitative PCR for rare species detection
    Xia, Zhiqiang
    Johansson, Mattias L.
    Gao, Yangchun
    Zhang, Lei
    Haffner, Gordon Douglas
    MacIsaac, Hugh J.
    Zhan, Aibin
    ECOLOGY AND EVOLUTION, 2018, 8 (23): : 11799 - 11807
  • [6] Quantitative real-time PCR is not more sensitive than "Conventional" PCR
    Bastien, Patrick
    Procop, Gary W.
    Reischl, Udo
    JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (06) : 1897 - 1900
  • [7] Development of Quantitative Real-Time PCR Assays for Rapid and Sensitive Detection of Two Badnavirus Species in Sugarcane
    Sun, Sheng-Ren
    Ahmad, Kashif
    Wu, Xiao-Bin
    Chen, Jian-Sheng
    Fu, Hua-Ying
    Huang, Mei-Ting
    Gao, San-Ji
    BIOMED RESEARCH INTERNATIONAL, 2018, 2018
  • [8] Rapid and accurate determination of zygosity in transgenic animals by real-time quantitative PCR
    Tesson, L
    Heslan, JM
    Ménoret, S
    Anegon, I
    TRANSGENIC RESEARCH, 2002, 11 (01) : 43 - 48
  • [9] Quantitative real-time PCR for rapid and accurate titration of recombinant baculovirus particles
    Hitchman, Richard B.
    Siaterli, Evangelia A.
    Nixon, Clare P.
    King, Linda A.
    BIOTECHNOLOGY AND BIOENGINEERING, 2007, 96 (04) : 810 - 814
  • [10] Rapid and accurate determination of zygosity in transgenic animals by real-time quantitative PCR
    Laurent Tesson
    Jean-Marie Heslan
    Séverine Ménoret
    Ignacio Anegon
    Transgenic Research, 2002, 11 : 43 - 48