Ivanova Natalia V, Kuzmina Maria L, Braukmann Thomas W A, Borisenko Alex V, Zakharov Evgeny V
Centre for Biodiversity Genomics, Biodiversity Institute of Ontario, University of Guelph, Guelph, Ontario, Canada.
PLoS One. 2016 May 26;11(5):e0156426. doi: 10.1371/journal.pone.0156426. eCollection 2016.
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.
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.
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.
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.
基于DNA的检测作为一种用于多种食品认证的工具已逐渐被接受;然而,其在草药补充剂检测中的适用性仍存在争议。
我们利用桑格测序法和新一代测序(NGS)对来自三种不同生产商的15种草药补充剂进行分类鉴定,这些补充剂源自五种药用植物:紫锥菊、缬草、银杏、贯叶连翘和胡芦巴。实验设计包括DNA提取的三种改进方法、两种裂解液稀释方法、内部扩增对照以及多个阴性对照以排除背景污染。还使用高效液相色谱 - 质谱联用(HPLC - MS)分析银杏补充剂中活性药用成分的存在情况。
所有补充剂均产生了来自多个物种的DNA,使得rbcL和ITS2区域的桑格测序结果在实验重复之间无法解读或不可重复。总体而言,在八种干草药形式的补充剂中,有七种成功检测到了制造商列出的药用植物的DNA;然而,在大多数植物提取物中观察到由于降解导致的DNA回收率低或不佳(桑格测序法未检测到任何DNA;NGS法在七种中有三种检测到)。NGS还揭示了一个多样的真菌群落,已知这些真菌与活植物材料和/或植物提取物生产中使用的发酵过程有关。HPLC - MS检测表明,DNA降解的银杏补充剂含有十种关键药用成分。
草药补充剂的质量控制应采用针对DNA和生物活性成分的协同方法,特别是对于DNA降解的标准化提取物。本研究中开发的NGS工作流程能够可靠地检测植物和真菌DNA,制造商可将其用于原材料的质量保证、生产过程中的污染控制以及最终产品。结果的解释应采用跨学科方法,考虑到草药补充剂生产过程中涉及的过程以及植物 - 植物和植物 - 真菌生物相互作用的生物复杂性。