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Authentication of Herbal Supplements Using Next-Generation Sequencing

BACKGROUND: DNA-based testing has been gaining acceptance as a tool for authentication of a wide range of food products; however, its applicability for testing of herbal supplements remains contentious. METHODS: We utilized Sanger and Next-Generation Sequencing (NGS) for taxonomic authentication of...

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Autores principales: Ivanova, Natalia V., Kuzmina, Maria L., Braukmann, Thomas W. A., Borisenko, Alex V., Zakharov, Evgeny V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882080/
https://www.ncbi.nlm.nih.gov/pubmed/27227830
http://dx.doi.org/10.1371/journal.pone.0156426
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author Ivanova, Natalia V.
Kuzmina, Maria L.
Braukmann, Thomas W. A.
Borisenko, Alex V.
Zakharov, Evgeny V.
author_facet Ivanova, Natalia V.
Kuzmina, Maria L.
Braukmann, Thomas W. A.
Borisenko, Alex V.
Zakharov, Evgeny V.
author_sort Ivanova, Natalia V.
collection PubMed
description BACKGROUND: DNA-based testing has been gaining acceptance as a tool for authentication of a wide range of food products; however, its applicability for testing of herbal supplements remains contentious. METHODS: We utilized Sanger and Next-Generation Sequencing (NGS) for taxonomic authentication of fifteen herbal supplements representing three different producers from five medicinal plants: Echinacea purpurea, Valeriana officinalis, Ginkgo biloba, Hypericum perforatum and Trigonella foenum-graecum. Experimental design included three modifications of DNA extraction, two lysate dilutions, Internal Amplification Control, and multiple negative controls to exclude background contamination. Ginkgo supplements were also analyzed using HPLC-MS for the presence of active medicinal components. RESULTS: All supplements yielded DNA from multiple species, rendering Sanger sequencing results for rbcL and ITS2 regions either uninterpretable or non-reproducible between the experimental replicates. Overall, DNA from the manufacturer-listed medicinal plants was successfully detected in seven out of eight dry herb form supplements; however, low or poor DNA recovery due to degradation was observed in most plant extracts (none detected by Sanger; three out of seven–by NGS). NGS also revealed a diverse community of fungi, known to be associated with live plant material and/or the fermentation process used in the production of plant extracts. HPLC-MS testing demonstrated that Ginkgo supplements with degraded DNA contained ten key medicinal components. CONCLUSION: Quality control of herbal supplements should utilize a synergetic approach targeting both DNA and bioactive components, especially for standardized extracts with degraded DNA. The NGS workflow developed in this study enables reliable detection of plant and fungal DNA and can be utilized by manufacturers for quality assurance of raw plant materials, contamination control during the production process, and the final product. Interpretation of results should involve an interdisciplinary approach taking into account the processes involved in production of herbal supplements, as well as biocomplexity of plant-plant and plant-fungal biological interactions.
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spelling pubmed-48820802016-06-10 Authentication of Herbal Supplements Using Next-Generation Sequencing Ivanova, Natalia V. Kuzmina, Maria L. Braukmann, Thomas W. A. Borisenko, Alex V. Zakharov, Evgeny V. PLoS One Research Article BACKGROUND: DNA-based testing has been gaining acceptance as a tool for authentication of a wide range of food products; however, its applicability for testing of herbal supplements remains contentious. METHODS: We utilized Sanger and Next-Generation Sequencing (NGS) for taxonomic authentication of fifteen herbal supplements representing three different producers from five medicinal plants: Echinacea purpurea, Valeriana officinalis, Ginkgo biloba, Hypericum perforatum and Trigonella foenum-graecum. Experimental design included three modifications of DNA extraction, two lysate dilutions, Internal Amplification Control, and multiple negative controls to exclude background contamination. Ginkgo supplements were also analyzed using HPLC-MS for the presence of active medicinal components. RESULTS: All supplements yielded DNA from multiple species, rendering Sanger sequencing results for rbcL and ITS2 regions either uninterpretable or non-reproducible between the experimental replicates. Overall, DNA from the manufacturer-listed medicinal plants was successfully detected in seven out of eight dry herb form supplements; however, low or poor DNA recovery due to degradation was observed in most plant extracts (none detected by Sanger; three out of seven–by NGS). NGS also revealed a diverse community of fungi, known to be associated with live plant material and/or the fermentation process used in the production of plant extracts. HPLC-MS testing demonstrated that Ginkgo supplements with degraded DNA contained ten key medicinal components. CONCLUSION: Quality control of herbal supplements should utilize a synergetic approach targeting both DNA and bioactive components, especially for standardized extracts with degraded DNA. The NGS workflow developed in this study enables reliable detection of plant and fungal DNA and can be utilized by manufacturers for quality assurance of raw plant materials, contamination control during the production process, and the final product. Interpretation of results should involve an interdisciplinary approach taking into account the processes involved in production of herbal supplements, as well as biocomplexity of plant-plant and plant-fungal biological interactions. Public Library of Science 2016-05-26 /pmc/articles/PMC4882080/ /pubmed/27227830 http://dx.doi.org/10.1371/journal.pone.0156426 Text en © 2016 Ivanova et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ivanova, Natalia V.
Kuzmina, Maria L.
Braukmann, Thomas W. A.
Borisenko, Alex V.
Zakharov, Evgeny V.
Authentication of Herbal Supplements Using Next-Generation Sequencing
title Authentication of Herbal Supplements Using Next-Generation Sequencing
title_full Authentication of Herbal Supplements Using Next-Generation Sequencing
title_fullStr Authentication of Herbal Supplements Using Next-Generation Sequencing
title_full_unstemmed Authentication of Herbal Supplements Using Next-Generation Sequencing
title_short Authentication of Herbal Supplements Using Next-Generation Sequencing
title_sort authentication of herbal supplements using next-generation sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882080/
https://www.ncbi.nlm.nih.gov/pubmed/27227830
http://dx.doi.org/10.1371/journal.pone.0156426
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