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Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures
DNA barcoding has been used for decades, although it has mostly been applied to some single-species. Traditional Chinese medicine (TCM), which is mainly used in the form of combination-one type of the multi-species, identification is crucial for clinical usage. Next-generation Sequencing (NGS) has b...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562688/ https://www.ncbi.nlm.nih.gov/pubmed/31067783 http://dx.doi.org/10.3390/genes10050343 |
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author | Zhang, Peng Liu, Chunsheng Zheng, Xiasheng Wu, Lan Liu, Zhixiang Liao, Baosheng Shi, Yuhua Li, Xiwen Xu, Jiang Chen, Shilin |
author_facet | Zhang, Peng Liu, Chunsheng Zheng, Xiasheng Wu, Lan Liu, Zhixiang Liao, Baosheng Shi, Yuhua Li, Xiwen Xu, Jiang Chen, Shilin |
author_sort | Zhang, Peng |
collection | PubMed |
description | DNA barcoding has been used for decades, although it has mostly been applied to some single-species. Traditional Chinese medicine (TCM), which is mainly used in the form of combination-one type of the multi-species, identification is crucial for clinical usage. Next-generation Sequencing (NGS) has been used to address this authentication issue for the past few years, but conventional NGS technology is hampered in application due to its short sequencing reads and systematic errors. Here, a novel method, Full-length multi-barcoding (FLMB) via long-read sequencing, is employed for the identification of biological compositions in herbal compound formulas in adequate and well controlled studies. By directly sequencing the full-length amplicons of ITS2 and psbA-trnH through single-molecule real-time (SMRT) technology, the biological composition of a classical prescription Sheng-Mai-San (SMS) was analyzed. At the same time, clone-dependent Sanger sequencing was carried out as a parallel control. Further, another formula—Sanwei-Jili-San (SJS)—was analyzed with genes of ITS2 and CO1. All the ingredients in the samples of SMS and SJS were successfully authenticated at the species level, and 11 exogenous species were also checked, some of which were considered as common contaminations in these products. Methodology analysis demonstrated that this method was sensitive, accurate and reliable. FLMB, a superior but feasible approach for the identification of biological complex mixture, was established and elucidated, which shows perfect interpretation for DNA barcoding that could lead its application in multi-species mixtures. |
format | Online Article Text |
id | pubmed-6562688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65626882019-06-17 Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures Zhang, Peng Liu, Chunsheng Zheng, Xiasheng Wu, Lan Liu, Zhixiang Liao, Baosheng Shi, Yuhua Li, Xiwen Xu, Jiang Chen, Shilin Genes (Basel) Article DNA barcoding has been used for decades, although it has mostly been applied to some single-species. Traditional Chinese medicine (TCM), which is mainly used in the form of combination-one type of the multi-species, identification is crucial for clinical usage. Next-generation Sequencing (NGS) has been used to address this authentication issue for the past few years, but conventional NGS technology is hampered in application due to its short sequencing reads and systematic errors. Here, a novel method, Full-length multi-barcoding (FLMB) via long-read sequencing, is employed for the identification of biological compositions in herbal compound formulas in adequate and well controlled studies. By directly sequencing the full-length amplicons of ITS2 and psbA-trnH through single-molecule real-time (SMRT) technology, the biological composition of a classical prescription Sheng-Mai-San (SMS) was analyzed. At the same time, clone-dependent Sanger sequencing was carried out as a parallel control. Further, another formula—Sanwei-Jili-San (SJS)—was analyzed with genes of ITS2 and CO1. All the ingredients in the samples of SMS and SJS were successfully authenticated at the species level, and 11 exogenous species were also checked, some of which were considered as common contaminations in these products. Methodology analysis demonstrated that this method was sensitive, accurate and reliable. FLMB, a superior but feasible approach for the identification of biological complex mixture, was established and elucidated, which shows perfect interpretation for DNA barcoding that could lead its application in multi-species mixtures. MDPI 2019-05-07 /pmc/articles/PMC6562688/ /pubmed/31067783 http://dx.doi.org/10.3390/genes10050343 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Peng Liu, Chunsheng Zheng, Xiasheng Wu, Lan Liu, Zhixiang Liao, Baosheng Shi, Yuhua Li, Xiwen Xu, Jiang Chen, Shilin Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title | Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title_full | Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title_fullStr | Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title_full_unstemmed | Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title_short | Full-Length Multi-Barcoding: DNA Barcoding from Single Ingredient to Complex Mixtures |
title_sort | full-length multi-barcoding: dna barcoding from single ingredient to complex mixtures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562688/ https://www.ncbi.nlm.nih.gov/pubmed/31067783 http://dx.doi.org/10.3390/genes10050343 |
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