Yunnan Branch, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Jinghong 666100, China; Key Laborartory of Dai and Southern Medicine of Xishuangbanna Dai Autonomous Prefecture, Jinghong 666100, China.
Key Lab of Chinese Medicine Resources Conservation, State Administration of Traditional Chinese Medicine of the People's Republic of China, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China; Engineering Research Center of Tradition Chinese Medicine Resource, Ministry of Education, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.
Chin J Nat Med. 2020 Aug;18(8):594-605. doi: 10.1016/S1875-5364(20)30071-6.
To ensure the safety of medications, it is vital to accurately authenticate species of the Apocynaceae family, which is rich in poisonous medicinal plants. We identified Apocynaceae species by using nuclear internal transcribed spacer 2 (ITS2) and psbA-trnH based on experimental data. The identification ability of ITS2 and psbA-trnH was assessed using specific genetic divergence, BLAST1, and neighbor-joining trees. For DNA barcoding, ITS2 and psbA-trnH regions of 122 plant samples of 31 species from 19 genera in the Apocynaceae family were amplified. The PCR amplification for ITS2 and psbA-trnH sequences was 100%. The sequencing success rates for ITS2 and psbA-trnH sequences were 81% and 61%, respectively. Additional data involved 53 sequences of the ITS2 region and 38 sequences of the psbA-trnH region were downloaded from GenBank. Moreover, the analysis showed that the inter-specific divergence of Apocynaceae species was greater than its intra-specific variations. The results indicated that, using the BLAST1 method, ITS2 showed a high identification efficiency of 97% and 100% of the samples at the species and genus levels, respectively, via BLAST1, and psbA-trnH successfully identified 95% and 100% of the samples at the species and genus levels, respectively. The barcode combination of ITS2/psbA-trnH successfully identified 98% and 100% of samples at the species and genus levels, respectively. Subsequently, the neighbor joining tree method also showed that barcode ITS2 and psbA-trnH could distinguish among the species within the Apocynaceae family. ITS2 is a core barcode and psbA-trnH is a supplementary barcode for identifying species in the Apocynaceae family. These results will help to improve DNA barcoding reference databases for herbal drugs and other herbal raw materials.
为确保药物安全,准确鉴定夹竹桃科(富含有毒药用植物)物种至关重要。我们根据实验数据,利用核内转录间隔区 2(ITS2)和 psbA-trnH 来鉴定夹竹桃科物种。通过特定遗传分歧、BLAST1 和邻接法树评估了 ITS2 和 psbA-trnH 的鉴定能力。对于 DNA 条形码,我们扩增了夹竹桃科 19 属 31 种 122 个植物样本的 ITS2 和 psbA-trnH 区。ITS2 和 psbA-trnH 序列的 PCR 扩增成功率均为 100%。ITS2 和 psbA-trnH 序列的测序成功率分别为 81%和 61%。从 GenBank 下载了额外的 53 个 ITS2 区序列和 38 个 psbA-trnH 区序列。此外,分析表明,夹竹桃科物种的种间差异大于种内变异。结果表明,使用 BLAST1 方法,ITS2 在物种和属水平的鉴定效率分别高达 97%和 100%,psbA-trnH 成功鉴定了 95%和 100%的物种和属水平的样本。ITS2/psbA-trnH 条形码组合分别成功鉴定了 98%和 100%的物种和属水平的样本。随后,邻接法树方法也表明,条形码 ITS2 和 psbA-trnH 可以区分夹竹桃科内的物种。ITS2 是核心条形码,psbA-trnH 是鉴定夹竹桃科物种的补充条形码。这些结果将有助于提高草药和其他草药原料的 DNA 条形码参考数据库。