Nanopore environmental DNA sequencing of catch water for estimating species composition in demersal bottom trawl fisheries

Q1 Agricultural and Biological Sciences
Environmental DNA Pub Date : 2024-05-07 DOI:10.1002/edn3.555
Sara Maggini, Magnus Wulff Jacobsen, Paulina Urban, Brian Klitgaard Hansen, Jos Kielgast, Dorte Bekkevold, Ernesto Jardim, Jann T. Martinsohn, Gary R. Carvalho, Einar E. Nielsen, Alexander S. T. Papadopulos
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引用次数: 0

Abstract

Bycatch and discards, representing unwanted catches, undermine sustainable fisheries and hinder the conservation of vulnerable and endangered species. To effectively monitor bycatch and enhance the effectiveness of management measures while promoting sustainable fishing practices, reliable data is essential. Here, we explore the use of Nanopore metabarcoding to analyze the catch composition in demersal bottom fisheries. We collected eDNA samples directly from an onboard catch holding tank (catch water) for 10 fishing hauls from a fishing vessel operating in the Skagerrak (North-East Atlantic). The approach involved sequencing a combination of long (~2 kb) and short (~170–313 bp) mitochondrial amplicons and was validated by analyzing a fishery-related mock community sample and fishing haul replicates. Overall, the detection rate accuracy was 95% for landed species, and replicates obtained from the same fishing haul showed consistent results, validating the robustness of this approach. The detection rate accuracy for all caught species observed on board (including the non-landed fraction) was 81%. Undetected species were always limited to species in low abundance, but may also be attributed to problems with identifying closely related species due to the impact of sequencing errors and limited diagnostic variation in the genetic regions used. In the future, such biases may be reduced by using additional markers to increase species discrimination power and applying newly available technological advantages in flow cell chemistry to improve sequencing accuracy. In conclusion, this study demonstrates the effectiveness of Nanopore eDNA sequencing of catch water for estimating species composition in demersal bottom trawl fisheries, including catches of non-commercial and threatened and vulnerable species, without disrupting fishing activities. Incorporating eDNA analysis of catch water may therefore help facilitate effective monitoring, leading to better-informed fisheries management, biodiversity conservation efforts, and the implementation of relevant legislation such as the EU landing obligation.

Abstract Image

对捕捞水进行纳米孔环境 DNA 测序,以估算底层拖网渔业的物种组成
兼捕渔获物和弃鱼代表无用的渔获物,它们破坏了可持续渔业,阻碍了对脆弱和濒危物种的保护。为了有效监测副渔获物,提高管理措施的有效性,同时促进可持续渔业实践,可靠的数据至关重要。在此,我们探索使用纳米孔代谢编码来分析底层捕捞的渔获物组成。我们直接从一艘在斯卡格拉克海峡(东北大西洋)作业的渔船上的渔获物储藏箱(渔获水)中收集了 10 次捕捞的 eDNA 样本。该方法包括对长的(约 2 kb)和短的(约 170-313 bp)线粒体扩增子进行测序,并通过分析与渔业相关的模拟群落样本和捕捞重复样本进行验证。总体而言,上岸物种的检测准确率为 95%,从同一渔场获得的重复样本显示出一致的结果,验证了该方法的稳健性。船上观察到的所有捕获物种(包括未上岸部分)的检测准确率为 81%。未检测到的物种总是局限于丰度较低的物种,但也可能是由于测序错误的影响和所使用基因区域的有限诊断变异导致的近缘物种识别问题。今后,可通过使用更多标记物来提高物种鉴别力,并应用流式细胞化学的新技术优势来提高测序准确性,从而减少此类偏差。总之,本研究证明了纳米孔 eDNA 测序对底层底拖网渔业物种组成(包括非商业物种和受威胁及脆弱物种的渔获量)估算的有效性,且不会干扰渔业活动。因此,对渔获水进行 eDNA 分析有助于促进有效监测,从而实现更明智的渔业管理、生物多样性保护工作以及相关法律(如欧盟上岸义务)的实施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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