California Department of Water Resources, Sacramento, CA, USA.
Department of Animal Science, University of California Davis, Davis, CA, USA.
Mol Ecol Resour. 2020 Jul;20(4):961-970. doi: 10.1111/1755-0998.13186. Epub 2020 Jun 13.
One of the most fundamental aspects of ecological research and monitoring is accurate species identification, but cryptic speciation and observer error can confound phenotype-based identification. The CRISPR-Cas toolkit has facilitated remarkable advances in many scientific disciplines, but the fields of ecology and conservation biology have yet to fully embrace this powerful technology. The recently developed CRISPR-Cas13a platform SHERLOCK (Specific High-sensitivity Enzymatic Reporter unLOCKing) enables highly accurate taxonomic identification and has all the characteristics needed to transition to ecological and environmental disciplines. Here we conducted a series of "proof of principle" experiments to characterize SHERLOCK's ability to accurately, sensitively and rapidly distinguish three fish species of management interest co-occurring in the San Francisco Estuary that are easily misidentified in the field. We improved SHERLOCK's ease of field deployment by combining the previously demonstrated rapid isothermal amplification and CRISPR genetic identification with a minimally invasive and extraction-free DNA collection protocol, as well as the option of instrument-free lateral flow detection. This approach opens the door for redefining how, where and by whom genetic identifications occur in the future.
生态研究和监测中最基本的方面之一是准确的物种鉴定,但隐种形成和观察者误差会混淆基于表型的鉴定。CRISPR-Cas 工具包促成了许多科学学科的显著进步,但生态学和保护生物学领域尚未完全接受这项强大的技术。最近开发的 CRISPR-Cas13a 平台 SHERLOCK(Specific High-sensitivity Enzymatic Reporter unLOCKing)可实现高度准确的分类鉴定,并且具有过渡到生态和环境学科所需的所有特征。在这里,我们进行了一系列“原理验证”实验,以表征 SHERLOCK 区分在旧金山湾同时存在的三种具有管理意义的鱼类物种的能力,这些鱼类在野外很容易被错误识别。我们通过将以前展示的快速等温扩增和 CRISPR 基因鉴定与微创且无需提取的 DNA 收集方案以及无仪器的侧流检测选项相结合,提高了 SHERLOCK 在野外的部署便利性。这种方法为重新定义未来在何处、如何以及由谁进行基因鉴定开辟了道路。