Department of Population Health and Pathobiology, North Carolina State University, College of Veterinary Medicine, Raleigh, North Carolina, United States of America.
PLoS One. 2020 Apr 16;15(4):e0231436. doi: 10.1371/journal.pone.0231436. eCollection 2020.
Molecular-based taxonomy, specifically DNA barcoding, has streamlined organism identification. For land plants, the recommended 2-locus barcode of rbcL and matK is not suitable for all groups, thus the second subunit of the nuclear internal transcribed spacer (ITS2) has received attention as a possible alternative. To date, evaluations of ITS2 have mostly been limited in scope to specific plant orders/families and single source material. Prior to using ITS2 to routinely characterize land plants present in environmental samples (i.e., DNA metabarcoding), a wet lab protocol optimized for bulk sample types is needed. To address this gap, in this study we determined the broad recoverability across land plants when using published ITS2 primer pairs, and subsequently optimized the PCR reaction constituents and cycling conditions for the best two performing primer pairs (ITS2F/ITSp4 and ITSp3/ITSu4). Using these conditions, both primer pairs were used to characterize land plants present in 17 diverse soils collected from across the US. The resulting PCR amplicons were prepared into libraries and pooled for sequencing on an Illumina® MiniSeq. Our existing bioinformatics workflow was used to process raw sequencing data and taxonomically assign unique ITS2 plant sequences by comparison to GenBank. Given strict quality criteria were imposed on sequences for inclusion in data analysis, only 43.6% and 7.5% of sequences from ITS2F/ITSp4 and ITSp3/ITSu4 respectively remained for taxonomic comparisons; ~7-11% of sequences originated from fungal co-amplification. The number of orders and families recovered did differ between primer pairs, with ITS2F/ITSp4 consistently outperforming ITSp3/ITSu4 by >15%. Primer pair bias was observed in the recovery of certain taxonomic groups; ITS2F/ITSp4 preferentially recovered flowering plants and grasses, whereas ITSp3/ITSu4 recovered more moss taxa. To maximize data recovery and reduce potential bias, we advocate that studies using ITS2 to characterize land plants from environmental samples such as soil use a multiple primer pair approach.
基于分子的分类学,特别是 DNA 条形码,简化了生物鉴定。对于陆地植物,推荐的 rbcL 和 matK 双基因条形码并不适合所有类群,因此核内转录间隔区(ITS2)的第二个亚基受到关注,可能成为替代方法。迄今为止,对 ITS2 的评估大多仅限于特定的植物目/科和单一来源材料。在使用 ITS2 对环境样本中的陆地植物进行常规特征描述(即 DNA 宏条形码)之前,需要优化适用于批量样本类型的实验室方案。为了解决这一差距,本研究确定了使用已发表的 ITS2 引物对时陆地植物的广泛可恢复性,随后优化了最佳的两个表现引物对(ITS2F/ITSp4 和 ITSp3/ITSu4)的 PCR 反应成分和循环条件。使用这些条件,我们使用这两个引物对来描述来自美国各地的 17 种不同土壤中的陆地植物。所得 PCR 扩增子被制备成文库,并在 Illumina®MiniSeq 上进行测序。我们现有的生物信息学工作流程用于处理原始测序数据,并通过与 GenBank 比较对唯一的 ITS2 植物序列进行分类分配。由于对包括在数据分析中的序列施加了严格的质量标准,只有 ITS2F/ITSp4 和 ITSp3/ITSu4 的序列分别有 43.6%和 7.5%保留用于分类比较;~7-11%的序列源自真菌的共同扩增。引物对之间回收的目和科的数量确实不同,ITS2F/ITSp4 的表现始终优于 ITSp3/ITSu4,超过 15%。在某些分类群的回收中观察到引物对的偏好性;ITS2F/ITSp4 优先回收开花植物和草类,而 ITSp3/ITSu4 回收了更多的苔藓类群。为了最大限度地提高数据恢复并减少潜在偏差,我们主张使用 ITS2 对土壤等环境样本中的陆地植物进行特征描述的研究使用多引物对方法。