用于水生入侵物种监测的高通量qPCR芯片SmartScreen-AIS

IF 6.2 Q1 Agricultural and Biological Sciences
John A. Kronenberger, Taylor M. Wilcox, Michael K. Schwartz
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引用次数: 0

摘要

有效的野生动物保护需要频繁和广泛的物种发生数据。随着基于eDNA的监测技术的成熟——现在被广泛认为是敏感的、成本有效的和合法的——全国协调的eDNA战略开始形成。这种雄心勃勃的计划将需要eDNA分析,其吞吐量和灵敏度需要在广泛的地理范围内监测许多受保护的,致病的和入侵的物种。在这里,我们通过SmartScreen-AIS来满足这一需求:一种高通量qPCR (HT-qPCR)芯片,具有46项针对广泛关注的水生入侵物种的检测。经过验证,SmartScreen-AIS可以在美国大陆使用,并且可以根据需要细分为更小的芯片格式,用于特定地区或生物群系。与传统qPCR相比,HT-qPCR的检测性能较强,在某些情况下特异性略低(由于预扩增),但灵敏度明显较高。污染是罕见的,PCR抑制最小到不存在,并且在三个军事设施的演示中检测到芯片上已知存在的所有物种的eDNA,以及以前未记录的一个物种。成本的节省将取决于所使用的分析方法的数量和测试的样品,但在这项研究中,我们估计使用HT-qPCR进行eDNA分析比使用我们的传统qPCR方案便宜75%。为了方便使用,我们提供了分析细节的附录、工作台协议、处理结果的脚本和包含国家级分析特异性信息的在线应用程序。SmartScreen-AIS有潜力在美国推进入侵物种的早期检测,我们希望我们的HT-qPCR工作流程能激发芯片的开发和全球使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

SmartScreen-AIS: A High-Throughput qPCR Chip for Nationwide Surveillance of Aquatic Invasive Species

SmartScreen-AIS: A High-Throughput qPCR Chip for Nationwide Surveillance of Aquatic Invasive Species

Effective wildlife conservation requires frequent and widespread data on species occurrence. With the maturation of eDNA-based monitoring—now widely recognized as sensitive, cost effective, and legally defensible—nationally coordinated eDNA strategies are beginning to take shape. Such ambitious initiatives will require eDNA analytics with the throughput and sensitivity required for surveillance of many protected, pathogenic, and invasive species across broad geographic scales. Here, we help meet this need with SmartScreen-AIS: a high-throughput qPCR (HT-qPCR) chip with 46 assays targeting aquatic invasive species of widespread concern. SmartScreen-AIS was validated for use throughout the continental United States and can be subdivided into smaller chip formats as desired for use in specific regions or biomes. Assay performance in HT-qPCR was strong relative to conventional qPCR, with slightly lower specificity in some cases (due to pre-amplification) but significantly higher sensitivity. Contamination was rare, PCR inhibition was minimal to nonexistent, and demonstration at three military installations detected eDNA from all species on the chip that were known to be present and one species that was previously undocumented. Cost savings will depend on the number of assays used and samples tested, but in this study we estimate that eDNA analyses were 75% cheaper using HT-qPCR than they would be with our conventional qPCR protocol. To facilitate use, we provide appendices with assay details, bench protocols, a script for processing results, and an online app with state-level assay specificity information. SmartScreen-AIS has the potential to advance early detection of invasive species in the United States, and we hope our HT-qPCR workflow inspires chip development and use globally.

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来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
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