Biodiversity Institute of Ontario, Department of Integrative Biology, University of Guelph, Guelph, Ontario, Canada.
PLoS One. 2011 Apr 13;6(4):e17497. doi: 10.1371/journal.pone.0017497.
Timely and accurate biodiversity analysis poses an ongoing challenge for the success of biomonitoring programs. Morphology-based identification of bioindicator taxa is time consuming, and rarely supports species-level resolution especially for immature life stages. Much work has been done in the past decade to develop alternative approaches for biodiversity analysis using DNA sequence-based approaches such as molecular phylogenetics and DNA barcoding. On-going assembly of DNA barcode reference libraries will provide the basis for a DNA-based identification system. The use of recently introduced next-generation sequencing (NGS) approaches in biodiversity science has the potential to further extend the application of DNA information for routine biomonitoring applications to an unprecedented scale. Here we demonstrate the feasibility of using 454 massively parallel pyrosequencing for species-level analysis of freshwater benthic macroinvertebrate taxa commonly used for biomonitoring. We designed our experiments in order to directly compare morphology-based, Sanger sequencing DNA barcoding, and next-generation environmental barcoding approaches. Our results show the ability of 454 pyrosequencing of mini-barcodes to accurately identify all species with more than 1% abundance in the pooled mixture. Although the approach failed to identify 6 rare species in the mixture, the presence of sequences from 9 species that were not represented by individuals in the mixture provides evidence that DNA based analysis may yet provide a valuable approach in finding rare species in bulk environmental samples. We further demonstrate the application of the environmental barcoding approach by comparing benthic macroinvertebrates from an urban region to those obtained from a conservation area. Although considerable effort will be required to robustly optimize NGS tools to identify species from bulk environmental samples, our results indicate the potential of an environmental barcoding approach for biomonitoring programs.
及时准确的生物多样性分析是生物监测计划成功的持续挑战。基于形态的生物指标类群鉴定既费时又费力,而且很少支持物种水平的分辨率,尤其是对于未成熟的生命阶段。在过去的十年中,已经做了大量的工作来开发替代方法,通过基于 DNA 序列的方法,如分子系统发育学和 DNA 条形码,进行生物多样性分析。正在进行的 DNA 条形码参考文库的组装将为基于 DNA 的鉴定系统提供基础。在生物多样性科学中使用最近引入的下一代测序(NGS)方法有可能将 DNA 信息的应用进一步扩展到常规生物监测应用,达到前所未有的规模。在这里,我们展示了使用 454 焦磷酸测序进行淡水底栖大型无脊椎动物生物监测常用类群的物种水平分析的可行性。我们设计了实验,以便直接比较基于形态的、Sanger 测序 DNA 条形码和下一代环境条形码方法。我们的结果表明,454 焦磷酸测序迷你条形码能够准确识别混合池中丰度超过 1%的所有物种。虽然该方法未能识别混合体中的 6 个稀有物种,但混合体中不存在个体的 9 个物种的序列提供了证据,表明基于 DNA 的分析可能在寻找大量环境样本中的稀有物种方面提供了有价值的方法。我们进一步通过比较城市地区和保护区的底栖大型无脊椎动物来展示环境条形码方法的应用。尽管需要大量的努力来稳健地优化 NGS 工具以从大量环境样本中识别物种,但我们的结果表明,环境条形码方法在生物监测计划中有应用潜力。