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阮惠婷, 王瑞丽, 李红婷, 刘丽, 匡天旭, 李敏, 邹柯姝. 2022: 不同采样方法和DNA提取方法对eDNA宏条形码技术监测河口鱼类多样性的影响. 动物学研究, 43(2): 192-204. DOI: 10.24272/j.issn.2095-8137.2021.331
引用本文: 阮惠婷, 王瑞丽, 李红婷, 刘丽, 匡天旭, 李敏, 邹柯姝. 2022: 不同采样方法和DNA提取方法对eDNA宏条形码技术监测河口鱼类多样性的影响. 动物学研究, 43(2): 192-204. DOI: 10.24272/j.issn.2095-8137.2021.331
Hui-Ting Ruan, Rui-Li Wang, Hong-Ting Li, Li Liu, Tian-Xu Kuang, Min Li, Ke-Shu Zou. 2022: Effects of sampling strategies and DNA extraction methods on eDNA metabarcoding: A case study of estuarine fish diversity monitoring. Zoological Research, 43(2): 192-204. DOI: 10.24272/j.issn.2095-8137.2021.331
Citation: Hui-Ting Ruan, Rui-Li Wang, Hong-Ting Li, Li Liu, Tian-Xu Kuang, Min Li, Ke-Shu Zou. 2022: Effects of sampling strategies and DNA extraction methods on eDNA metabarcoding: A case study of estuarine fish diversity monitoring. Zoological Research, 43(2): 192-204. DOI: 10.24272/j.issn.2095-8137.2021.331

不同采样方法和DNA提取方法对eDNA宏条形码技术监测河口鱼类多样性的影响

Effects of sampling strategies and DNA extraction methods on eDNA metabarcoding: A case study of estuarine fish diversity monitoring

  • 摘要: 环境DNA(eDNA)宏条形码技术是评估水生生态系统中物种组成和生物多样性的强有力工具,并已广泛应用于鱼类多样性的监测。然而,目前,用于监测鱼类多样性的eDNA技术尚未标准化。该研究分别比较了两种过滤方法、三种过滤水样体积以及三种DNA提取方法的DNA产出效果,以期为珠江口等人为干扰频繁的河口生态系统提供一种合适的基于eDNA的鱼类多样性监测方法。结果表明,与基于过滤的沉淀法相比,直接过滤法更适用于珠江口的eDNA宏条形码技术研究;DNeasy Blood and Tissue Kit(BT)和苯酚/氯仿(PC)提取方法具有较高的DNA产量、扩增子序列变体(ASV)丰度和香农多样性指数,并可以获得更均匀和一致的鱼类群落组成;其中,PC和BT分别在提取过滤水样体积为1000 mL和2000 mL时,获得更高的物种检测率、鱼类多样性和种类组成一致性。与底拖网相比,eDNA宏条形码技术在珠江口鱼类多样性调查中具有更高的灵敏度,监测到的种类数量更多,但两种方法在种类组成上具有一定的差异,二者的结合有利于提高鱼类多样性监测的准确性。这些结果表明,在河口生态系统的鱼类群落监测中,eDNA宏条形码技术流程中相关步骤的方法选择需要慎重考虑。

     

    Abstract: Environmental DNA (eDNA) integrated with metabarcoding is a promising and powerful tool for species composition and biodiversity assessment in aquatic ecosystems and is increasingly applied to evaluate fish diversity. To date, however, no standardized eDNA-based protocol has been established to monitor fish diversity. In this study, we investigated and compared two filtration methods and three DNA extraction methods using three filtration water volumes to determine a suitable approach for eDNA-based fish diversity monitoring in the Pearl River Estuary (PRE), a highly anthropogenically disturbed estuarine ecosystem. Compared to filtration-based precipitation, direct filtration was a more suitable method for eDNA metabarcoding in the PRE. The combined use of DNeasy Blood and Tissue Kit (BT) and traditional phenol/chloroform (PC) extraction produced higher DNA yields, amplicon sequence variants (ASVs), and Shannon diversity indices, and generated more homogeneous and consistent community composition among replicates. Compared to the other combined protocols, the PC and BT methods obtained better species detection, higher fish diversity, and greater consistency for the filtration water volumes of 1 000 and 2 000 mL, respectively. All eDNA metabarcoding protocols were more sensitive than bottom trawling in the PRE fish surveys and combining two techniques yielded greater taxonomic diversity. Furthermore, combining traditional methods with eDNA analysis enhanced accuracy. These results indicate that methodological decisions related to eDNA metabarcoding should be made with caution for fish community monitoring in estuarine ecosystems.

     

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