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A new versatile primer set targeting a short fragment of the mitochondrial COI region for metabarcoding metazoan diversity: application for characterizing coral reef fish gut contents

机译:一种针对线粒体COI区短片段的新通用引物组,用于metabarcoding后生动物多样性:表征珊瑚礁鱼肠内容物的应用

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Introduction The PCR-based analysis of homologous genes has become one of the most powerful approaches for species detection and identification, particularly with the recent availability of Next Generation Sequencing platforms (NGS) making it possible to identify species composition from a broad range of environmental samples. Identifying species from these samples relies on the ability to match sequences with reference barcodes for taxonomic identification. Unfortunately, most studies of environmental samples have targeted ribosomal markers, despite the fact that the mitochondrial Cytochrome c Oxidase subunit I gene (COI) is by far the most widely available sequence region in public reference libraries. This is largely because the available versatile (“universal”) COI primers target the 658 barcoding region, whose size is considered too large for many NGS applications. Moreover, traditional barcoding primers are known to be poorly conserved across some taxonomic groups. Results We first design a new PCR primer within the highly variable mitochondrial COI region, the “mlCOIintF” primer. We then show that this newly designed forward primer combined with the “jgHCO2198” reverse primer to target a 313 bp fragment performs well across metazoan diversity, with higher success rates than versatile primer sets traditionally used for DNA barcoding (i.e. LCO1490/HCO2198). Finally, we demonstrate how the shorter COI fragment coupled with an efficient bioinformatics pipeline can be used to characterize species diversity from environmental samples by pyrosequencing. We examine the gut contents of three species of planktivorous and benthivorous coral reef fish (family: Apogonidae and Holocentridae). After the removal of dubious COI sequences, we obtained a total of 334 prey Operational Taxonomic Units (OTUs) belonging to 14 phyla from 16 fish guts. Of these, 52.5% matched a reference barcode (>98% sequence similarity) and an additional 32% could be assigned to a higher taxonomic level using Bayesian assignment. Conclusions The molecular analysis of gut contents targeting the 313 COI fragment using the newly designed mlCOIintF primer in combination with the jgHCO2198 primer offers enormous promise for metazoan metabarcoding studies. We believe that this primer set will be a valuable asset for a range of applications from large-scale biodiversity assessments to food web studies.
机译:引言基于PCR的同源基因分析已成为物种检测和鉴定的最有力方法之一,尤其是随着近来下一代测序平台(NGS)的出现,使得可以从各种环境样品中鉴定物种组成。从这些样品中鉴定物种依赖于将序列与参考条形码进行匹配以进行生物分类鉴定的能力。不幸的是,尽管事实上线粒体细胞色素c氧化酶亚基I基因(COI)是迄今为止在公共参考文库中可获得的最广泛的序列区域,但大多数环境样品的研究都针对核糖体标记物。这主要是因为可用的通用(“通用”)COI引物靶向658条码区域,对于许多NGS应用来说,其大小被认为太大。此外,已知传统的条形码引物在某些分类学组中保守性很差。结果我们首先在高度可变的线粒体COI区域内设计了一种新的PCR引物,即“ mlCOIintF”引物。然后,我们表明,这种新设计的正向引物与“ jgHCO2198”反向引物结合,靶向313 bp片段,在后生动物多样性方面表现良好,比传统上用于DNA条形码的通用引物组(即LCO1490 / HCO2198)的成功率更高。最后,我们演示了如何将较短的COI片段与有效的生物信息学流水线相结合,通过焦磷酸测序来表征环境样品中的物种多样性。我们检查了三种食藻和底食珊瑚礁鱼(家族:A目科和鳞翅目科)的肠道含量。除去可疑的COI序列后,我们从16个鱼肠中获得了总共334个猎物操作分类单位(OTU),它们属于14个门。其中52.5%匹配参考条形码(> 98%的序列相似性),另外32%可以使用贝叶斯分配分配给更高的分类标准。结论使用新设计的mlCOIintF引物与jgHCO2198引物结合,对靶向313 COI片段的肠内容物进行分子分析,为后生超条形码研究提供了广阔的前景。我们认为,这套引物对从大规模生物多样性评估到食物网研究的一系列应用将是宝贵的资产。

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