School of Biosciences, Cardiff University, The Sir Martin Evans Building, Museum Avenue, Cardiff, CF10 3AX, UK.
RSPB Centre for Conservation Science, Royal Society for the Protection of Birds, The Lodge, Potton Road, Sandy, Bedfordshire, SG19 2DL, UK.
Sci Rep. 2018 Jun 4;8(1):8542. doi: 10.1038/s41598-018-26648-2.
DNA metabarcoding is a rapidly growing technique for obtaining detailed dietary information. Current metabarcoding methods for herbivory, using a single locus, can lack taxonomic resolution for some applications. We present novel primers for the second internal transcribed spacer of nuclear ribosomal DNA (ITS2) designed for dietary studies in Mauritius and the UK, which have the potential to give unrivalled taxonomic coverage and resolution from a short-amplicon barcode. In silico testing used three databases of plant ITS2 sequences from UK and Mauritian floras (native and introduced) totalling 6561 sequences from 1790 species across 174 families. Our primers were well-matched in silico to 88% of species, providing taxonomic resolution of 86.1%, 99.4% and 99.9% at the species, genus and family levels, respectively. In vitro, the primers amplified 99% of Mauritian (n = 169) and 100% of UK (n = 33) species, and co-amplified multiple plant species from degraded faecal DNA from reptiles and birds in two case studies. For the ITS2 region, we advocate taxonomic assignment based on best sequence match instead of a clustering approach. With short amplicons of 187-387 bp, these primers are suitable for metabarcoding plant DNA from faecal samples, across a broad geographic range, whilst delivering unparalleled taxonomic resolution.
DNA 代谢组学是一种获取详细饮食信息的快速发展技术。目前,使用单一基因座的食草动物代谢组学方法在某些应用中缺乏分类分辨率。我们提出了一种新的核核糖体 DNA(ITS2)内转录间隔区的引物,用于毛里求斯和英国的饮食研究,该引物具有从短扩增子条码获得无与伦比的分类覆盖和分辨率的潜力。计算机测试使用了来自英国和毛里求斯植物区系(本地和引入)的三个植物 ITS2 序列数据库,共有来自 174 个科的 1790 个物种的 6561 个序列。我们的引物在计算机上与 88%的物种很好地匹配,提供了 86.1%、99.4%和 99.9%的物种、属和科分类分辨率。在体外,引物扩增了 99%的毛里求斯(n=169)和 100%的英国(n=33)物种,并且在两项案例研究中,从爬行动物和鸟类的降解粪便 DNA 中共同扩增了多个植物物种。对于 ITS2 区域,我们主张基于最佳序列匹配而不是聚类方法进行分类分配。这些引物的扩增子长度为 187-387bp,适合对粪便样本中的植物 DNA 进行代谢组学分析,适用于广泛的地理范围,同时提供无与伦比的分类分辨率。