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PacBio amplicon sequencing for metabarcoding of mixed DNA samples from lichen herbarium specimens

机译:PacBio扩增子测序用于对地衣标本中的混合DNA样品进行超条形码编码

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摘要

The detection and identification of species of fungi in the environment using molecular methods heavily depends on reliable reference sequence databases. However, these databases are largely incomplete in terms of taxon coverage, and a significant effort is required from herbaria and living fungal collections for the mass-barcoding of well-identified and well-curated fungal specimens or strains. Here, a PacBio amplicon sequencing approach is applied to recent lichen herbarium specimens for the sequencing of the fungal ITS barcode, allowing a higher throughput sample processing than Sanger sequencing, which often required the use of cloning. Out of 96 multiplexed samples, a full-length ITS sequence of the target lichenised fungal species was recovered for 85 specimens. In addition, sequences obtained for co-amplified fungi gave an interesting insight into the diversity of endolichenic fungi. Challenges encountered at both the laboratory and bioinformatic stages are discussed, and cost and quality are compared with Sanger sequencing. With increasing data output and reducing sequencing cost, PacBio amplicon sequencing is seen as a promising approach for the generation of reference sequences for lichenised fungi as well as the characterisation of lichen-associated fungal communities.
机译:使用分子方法检测和鉴定环境中的真菌种类在很大程度上取决于可靠的参考序列数据库。但是,这些数据库在分类单元覆盖方面基本上是不完整的,需要大量的草药和活真菌收集物进行大量鉴定和精心挑选的真菌标本或菌株的大规模条形码编码。在此,将PacBio扩增子测序方法应用于最近的地衣植物标本室标本,以对真菌ITS条码进行测序,与通常需要使用克隆的Sanger测序相比,可提供更高的通量样品处理。在96个多重样本中,从85个样本中回收了目标苔藓样真菌物种的全长ITS序列。此外,获得的共扩增真菌序列对内分泌真菌的多样性提供了有趣的见解。讨论了在实验室和生物信息学阶段都遇到的挑战,并将成本和质量与Sanger测序进行了比较。随着数据输出的增加和测序成本的降低,PacBio扩增子测序被视为一种有前途的方法,可用于生成苔藓真菌的参考序列以及表征苔藓相关真菌群落。

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