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A broadly applicable COI primer pair and an efficient single‐tube amplicon library preparation protocol for metabarcoding

机译:适用于元条形码的广泛适用的COI引物对和有效的单管扩增子文库制备方案

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摘要

The nucleotide variation in the cytochrome c oxidase subunit I (COI) gene makes it ideal for assigning sequences to species. However, this variability also makes it difficult to design truly universal primers. Here, we present the forward primer “Sauron‐S878,” specifically designed to facilitate library preparation for metabarcoding. This primer is modified to improve the coverage of terrestrial species compared to the primer mCOIintF, optimized for aquatic systems, which raised the in silico coverage from 74.4% to 98.3% of available NCBI sequences (perfect match in 3′ region, up to three mismatches in remaining primer). When paired with the reverse primer “jgHCO2198” (fragment length ~313 bp), these primers amplified 98.4% of 255 tested DNA extracts from various taxa, which are better than many other common COI barcoding primers. Furthermore, a single‐tube protocol was developed, wherein these primers amplify the target gene, and attach MIDs and Illumina sequencing adapters in one reaction. This eliminates the need for re‐amplification or enzymatic ligation during library preparation while keeping the flexibility to modularly combine primers and MIDs. Using the single‐tube approach, three replicates of three mock samples were sequenced on a MiSeq platform with no adverse effects compared to commercial Nextera indexing kits. From this run, 75% of all included taxa could be recovered, with no considerable bias among taxonomic groups. Despite the fact that 98.4% of the extracts were confirmed to amplify in vitro, this number was lower than expected. A reason for this discrepancy was a clear link between the relative concentration of a specific DNA type in the template and the number of returned reads for this DNA. We would argue that such a bias may be especially problematic in metabarcoding where samples usually contain trace DNA in unknown amounts. However, how this affects the completeness of metabarcoding results has yet been poorly investigated.
机译:细胞色素C氧化酶亚基I(COI)基因的核苷酸变异使其非常适合为物种分配序列。然而,这种可变性也使得难以设计真正的通用引物。在这里,我们介绍了正向引物“ Sauron-S878”,该引物是专门为促进元条形码的文库制备而设计的。与为水生系统优化的引物mCOIintF相比,对该引物进行了改良以提高陆地物种的覆盖率,该引物对水生系统进行了优化,从而将计算机覆盖率从可用NCBI序列的74.4%提高到98.3%(在3'区域完全匹配,最多三个错配在剩余的底漆中)。当与反向引物“ jgHCO2198”(片段长度〜313 bp)配对时,这些引物扩增了255种来自各种分类群的DNA提取物的98.4%,比许多其他常见的COI条形码引物要好。此外,还开发了单管方案,其中这些引物可扩增靶基因,并在一个反应​​中连接MID和Illumina测序接头。这消除了文库制备过程中对重新扩增或酶促连接的需求,同时保持了灵活组合引物和MID的灵活性。使用单管方法,在MiSeq平台上对三个模拟样品的三个重复样品进行了测序,与商业Nextera索引试剂盒相比,没有不利影响。通过此操作,可以恢复所有包含的分类单元的75%,而分类组之间没有明显的偏差。尽管已确认有98.4%的提取物可在体外扩增,但这一数字低于预期。出现这种差异的原因是,模板中特定DNA类型的相对浓度与该DNA返回的读段数之间存在明确的联系。我们认为,这种偏向可能在元条形码中特别成问题,在条形码中,样品通常含有未知量的痕量DNA。但是,这如何影响元条形码结果的完整性尚未得到充分研究。

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