在浑浊水域中处理环境DNA样本的不同方法对鱼类、细菌和古菌群落有不同的影响

Rachel Turba, Glory H. Thai, David K. Jacobs
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引用次数: 0

摘要

沿海泻湖是加州特有物种和濒危物种的重要栖息地,这些物种受到城市化和日益严重的干旱的影响。环境DNA已被推广为一种有助于监测生物群落的方法,但为了克服所研究的独特系统所带来的挑战,不同的方案所引入的偏差仍有待了解。浑浊的水是这些系统中eDNA回收的一个方法挑战,因为它会迅速堵塞过滤器,阻止及时处理样品。我们调查了两种解决方案对群落组成的偏差,以克服由于浑浊而导致的缓慢过滤:过滤前冻结水(用于储存和长期处理),以及使用沉积物(与水样相反)。对两组引物12S(鱼)和16S(细菌和古菌)进行下游eDNA分析中群落组成的偏倚评估。结果表明,过滤前的冷冻水对每个引物的群落组成有不同的影响,当使用孔径较大(3 μm)的过滤器时,对16S的影响尤甚。然而,当关注鱼类群落时,冷冻前水样仍然可以作为储存和处理浑浊水样的可行选择(12S)。应谨慎使用沉积物样品作为处理水样的替代方法,并应至少增加生物重复的数量和/或取样量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Different approaches to processing environmental DNA samples in turbid waters have distinct effects for fish, bacterial and archaea communities
Coastal lagoons are an important habitat for endemic and threatened species in California that have suffered impacts from urbanization and increased drought. Environmental DNA has been promoted as a way to aid in the monitoring of biological communities, but much remains to be understood on the biases introduced by different protocols meant to overcome challenges presented by unique systems under study. Turbid water is one methodologic challenge to eDNA recovery in these systems as it quickly clogs filters, preventing timely processing of samples. We investigated biases in community composition produced by two solutions to overcome slow filtration due to turbidity: freezing of water prior to filtration (for storage purposes and long-term processing), and use of sediment (as opposed to water samples). Bias assessments of community composition in downstream eDNA analysis was conducted for two sets of primers, 12S (fish) and 16S (bacteria and archaea). Our results show that freezing water prior to filtration had different effects on community composition for each primer, especially for the 16S, when using a filter of larger pore size (3 μm). Nevertheless, pre-freezing water samples can still be a viable alternative for storage and processing of turbid water samples when focusing on fish communities (12S). The use of sediment samples as an alternative to processing water samples should be done with caution, and at minimum the number of biological replicates and/or volume sampled should be increased.
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