PCR-based rapid diagnostic tools for the authentication of medicinal mistletoe species

被引:13
|
作者
Noh, Pureum [1 ]
Kim, Wook Jin [1 ]
Yang, Sungyu [1 ]
Choi, Goya [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
Taxilli Herba; Visci Herba; Mistletoe; Maturase K; Molecular authentication; Sequence-characterized amplified region (SCAR) marker; DNA; SEQUENCE;
D O I
10.1016/j.phymed.2021.153667
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Taxilli Herba (TH) and Visci Herba (VH), defined as the leaves and branches of the mistletoe species Taxillus chinensis and Viscum coloratum, respectively, are popular herbal medicines in East Asia. However, commercial TH and VH products are frequently adulterated with related inauthentic mistletoe species, posing efficacy and safety concerns. Accurate species identification of herbal medicinal products is a prerequisite for quality control, but traditional morphological identification methods are hampered by difficulties in discriminating among closely related species and in identifying the source materials in processed products. Purpose: This study aimed to develop sequence-characterized amplified region (SCAR) markers and a multiplex-SCAR assay for rapid and accurate identification of authentic TH and VH. Methods: The matK region was sequenced in a total of 20 samples from five mistletoe species, namely T. chinensis and V. coloratum, and three species often found in adulterated herbal medicines, T. sutchuenensis, V. articulatum, and Macrosolen tricolor. Species-specific nucleotide polymorphisms were identified and short regions (21-22 bp) containing at least two species-specific nucleotides close to the 3' end were incorporated into SCAR primers that produced uniquely sized PCR amplicons for each species. The five SCAR primer sets were also combined into a multiplex-SCAR assay. Results: The SCAR primers successfully generated amplicons of the expected size for each target species even with low-DNA templates or with templates containing DNA from multiple samples. No amplification was observed in non-target species. The SCAR markers and the multiplex-SCAR assay successfully identified commercial TH and VH products that were counterfeit or adulterated in both dried and processed products. Conclusion: This is the first report to illustrate discrimination of genuine medicinal mistletoe species with DNA-based marker assays, enabling rapid and accurate species identification. The SCAR assays developed in this study will facilitate the standardization of commercial mistletoe products.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Authentication of closely related scombrid, catfish and tilapia species by PCR-based analysis and isoelectric focusing of parvalbumin
    Asadatun Abdullah
    Hartmut Rehbein
    European Food Research and Technology, 2015, 241 : 497 - 511
  • [32] PCR-based species identification of Agriotes larvae
    Staudacher, K.
    Pitterl, P.
    Furlan, L.
    Cate, P. C.
    Traugott, M.
    BULLETIN OF ENTOMOLOGICAL RESEARCH, 2011, 101 (02) : 201 - 210
  • [33] A PCR-BASED IDENTIFICATION METHOD FOR SPECIES OF ARMILLARIA
    HARRINGTON, TC
    WINGFIELD, BD
    MYCOLOGIA, 1995, 87 (02) : 280 - 288
  • [34] PCR-Based Identification of Oral Streptococcal Species
    Banas, Jeffrey A.
    Zhu, Min
    Dawson, Deborah V.
    Cao, Huojun
    Levy, Steven M.
    INTERNATIONAL JOURNAL OF DENTISTRY, 2016, 2016
  • [35] PCR-Based Identification of Toxinogenic Fusarium Species
    Lacmanova, Iva
    Pazlarova, Jarmila
    Kostelanska, Marta
    Hajslova, Jana
    CZECH JOURNAL OF FOOD SCIENCES, 2009, 27 : 90 - 94
  • [36] PCR-Based methods for identification ofEnterococcus species
    H. Drahovská
    D. Kocíncová
    M. Seman
    J. Turña
    Folia Microbiologica, 2002, 47 : 649 - 653
  • [37] PCR-based methods for identification of Enterococcus species
    Drahovská, H
    Kocíncová, D
    Seman, M
    Turna, J
    FOLIA MICROBIOLOGICA, 2002, 47 (06) : 649 - 653
  • [38] PCR-based diagnostic methods for 'Candidatus Liberibacter solanacearum'
    Mirmajlessi, Seyed Mahyar
    Sjolund, Maria Jennifer
    Mand, Marika
    Loiseau, Marianne
    Ilardi, Vincenza
    Haesaert, Geert
    Karise, Reet
    Gottsberger, Richard Alexander
    Sumner-Kalkun, Jason
    Bertaccini, Assunta
    PLANT PROTECTION SCIENCE, 2019, 55 (04) : 229 - 242
  • [39] PCR-based rapid genotyping of Stenotrophomonas maltophilia isolates
    Roscetto, Emanuela
    Rocco, Francesco
    Carlomagno, M. Stella
    Casalino, Mariassunta
    Colonna, Bianca
    Zarrilli, Raffaele
    Di Nocera, Pier Paolo
    BMC MICROBIOLOGY, 2008, 8 (1)
  • [40] PCR-based method for the rapid analysis of mRNA polyadenylation
    Yukinori Eguchi
    Tomoko Eguchi
    Biotechnology Letters, 2000, 22 : 1583 - 1586