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[Multiplex PCR method for simultaneous identification of Xanthii Fructus and its adulterants].
Zhang, Xiu-Mei; Li, Dan; Liu, Cong-Bin; Yu, Nian-Jun; Li, Yong-Jie; Xie, Dong-Mei.
Affiliation
  • Zhang XM; Anhui University of Chinese Medicine Hefei 230012, China.
  • Li D; Anhui University of Chinese Medicine Hefei 230012, China.
  • Liu CB; Anhui University of Chinese Medicine Hefei 230012, China.
  • Yu NJ; Anhui University of Chinese Medicine Hefei 230012, China Institute of Traditional Chinese Medicine Resources Protection and Development, Anhui Academy of Chinese Medicine Hefei 230012, China Anhui Province Key Laboratory of Research & Development of Chinese Medicine Hefei 230012, China.
  • Li YJ; the First Affiliated Hospital of Dalian Medical University Dalian 116011, China.
  • Xie DM; Anhui University of Chinese Medicine Hefei 230012, China Institute of Traditional Chinese Medicine Resources Protection and Development, Anhui Academy of Chinese Medicine Hefei 230012, China Anhui Province Key Laboratory of Research & Development of Chinese Medicine Hefei 230012, China.
Zhongguo Zhong Yao Za Zhi ; 47(10): 2605-2613, 2022 May.
Article in Zh | MEDLINE | ID: mdl-35718478
ABSTRACT
The purpose of this study is to establish a molecular method to identify Xanthii Fructus and two adulterants, the fruits of Xanthium mongolicum and X. italicum. Xanthii Fructus is the fruit of X. sibiricum, which is a Chinese herbal medicine used clinically to treat allergic rhinitis. The fruits of X. mongolicum and X. italicum have strong morphological similarities with Xanthii Fructus, while their safety of medication cannot be guaranteed. The genomes of X. sibiricum, X. mongolicum, and X. italicum were sequenced, which generated sequences of 2.21, 2.24, and 2.54 Gb, respectively. Based on the 76 specific contigs screened out by BLASTN and Bowtie 2, the corresponding primers were designed by Primer 5.0. Three pairs of primers with stable amplification efficiency and good reproducibility were screened out to establish a multiplex PCR method based on the PCR amplification results. Further, the annealing temperature, the amount of DNA template, the number of cycles, different DNA polymerases, and different PCR thermal cyclers were optimized. Fragments of 262 bp and 458 bp from X. sibiricum, 260, 454, and 927 bp from X. mongolicum, and 260 bp and 926 bp from X. italicum were amplified under the following conditions the annealing temperature of 52 ℃, 35 cycles, 30 ng template DNA. Then, the established method was used to detect 18 samples of X. sibiricum, 17 samples of X. mongolicum, and 12 samples of X. italicum. The results showed that all the samples had positive results, which were consistent with the morphological identification results, thus proving the stability and reliability of the established method. Combining genome sequencing technology and multiplex PCR method to identify Xanthii Fructus and its adulterants can not only obtain the difference in genetic background but also facilitate the design of reliable primers. The multiplex PCR have high specificity and repeatability, providing a new method for the molecular identification of Xanthii Fructus.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xanthium / Fruit Type of study: Diagnostic_studies / Prognostic_studies Language: Zh Journal: Zhongguo Zhong Yao Za Zhi Journal subject: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Xanthium / Fruit Type of study: Diagnostic_studies / Prognostic_studies Language: Zh Journal: Zhongguo Zhong Yao Za Zhi Journal subject: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Year: 2022 Document type: Article Affiliation country: