Asemaninejad Asma, Weerasuriya Nimalka, Gloor Gregory B, Lindo Zoë, Thorn R Greg
The University of Western Ontario, Department of Biology, London, Ontario, Canada N6A 5B7.
The University of Western Ontario, Department of Biochemistry, London, Ontario, Canada N6A 5B7.
PLoS One. 2016 Jul 8;11(7):e0159043. doi: 10.1371/journal.pone.0159043. eCollection 2016.
Metabarcoding has become an important tool in the discovery of biodiversity, including fungi, which are the second most speciose group of eukaryotes, with diverse and important ecological roles in terrestrial ecosystems. We have designed and tested new PCR primers that target the D1 variable region of nuclear large subunit (LSU) ribosomal DNA; one set that targets the phylum Ascomycota and another that recovers all other fungal phyla. The primers yield amplicons compatible with the Illumina MiSeq platform, which is cost-effective and has a lower error rate than other high throughput sequencing platforms. The new primer set LSU200A-F/LSU476A-R (Ascomycota) yielded 95-98% of reads of target taxa from environmental samples, and primers LSU200-F/LSU481-R (all other fungi) yielded 72-80% of target reads. Both primer sets have fairly low rates of data loss, and together they cover a wide variety of fungal taxa. We compared our results with these primers by amplifying and sequencing a subset of samples using the previously described ITS3_KYO2/ITS4_KYO3 primers, which amplify the internal transcribed spacer 2 (ITS2) of Ascomycota and Basidiomycota. With approximately equivalent read depth, our LSU primers recovered a greater number and phylogenetic diversity of sequences than the ITS2 primers. For instance, ITS3_KYO2/ITS4_KYO3 primers failed to pick up any members of Eurotiales, Mytilinidiales, Pezizales, Saccharomycetales, or Venturiales within Ascomycota, or members of Exobasidiomycetes, Microbotryomycetes, Pucciniomycetes, or Tremellomycetes within Basidiomycota, which were retrieved in good numbers from the same samples by our LSU primers. Among the OTUs recovered using the LSU primers were 127 genera and 28 species that were not obtained using the ITS2 primers, although the ITS2 primers recovered 10 unique genera and 16 species that were not obtained using either of the LSU primers These features identify the new primer sets developed in this study as useful complements to other universal primers for the study of fungal diversity and community composition.
代谢条形码已成为发现生物多样性的重要工具,其中包括真菌。真菌是第二大物种丰富的真核生物类群,在陆地生态系统中具有多样且重要的生态作用。我们设计并测试了针对核大亚基(LSU)核糖体DNA的D1可变区的新型PCR引物;一组针对子囊菌门,另一组可扩增所有其他真菌门。这些引物产生的扩增子与Illumina MiSeq平台兼容,该平台具有成本效益且错误率低于其他高通量测序平台。新引物组LSU200A - F/LSU476A - R(子囊菌门)从环境样本中获得了目标分类群95 - 98%的读数,引物LSU200 - F/LSU481 - R(所有其他真菌)获得了72 - 80%的目标读数。两组引物的数据丢失率都相当低,并且它们共同覆盖了广泛的真菌分类群。我们通过使用先前描述的ITS3_KYO2/ITS4_KYO3引物对一部分样本进行扩增和测序,将我们使用这些引物的结果进行了比较,ITS3_KYO2/ITS4_KYO3引物可扩增子囊菌门和担子菌门的内部转录间隔区2(ITS2)。在大致相同的读数深度下,我们的LSU引物比ITS2引物回收的序列数量更多且系统发育多样性更高。例如,ITS3_KYO2/ITS4_KYO3引物未能检测到子囊菌门中的散囊菌目、肉座菌目、盘菌目、酵母目或散囊菌目,或担子菌门中的外担菌纲、微黑粉菌纲、柄锈菌纲或银耳纲的任何成员,而我们的LSU引物从相同样本中大量检索到了这些成员。在使用LSU引物回收的操作分类单元(OTU)中,有127个属和28个物种未通过ITS2引物获得,尽管ITS2引物回收了10个独特的属和16个物种,这些物种未通过任何一组LSU引物获得。这些特性表明,本研究中开发的新引物组是研究真菌多样性和群落组成的其他通用引物的有用补充。