From DNA to biomass: opportunities and challenges in species quantification of bulk fisheries products

Author:

Hansen Brian Klitgaard1ORCID,Farrant Gregory Kevin2,Ogden Rob34,Humble Emily4,Ólafsdóttir Guðbjörg2,Bekkevold Dorte1ORCID,Knudsen Steen Wilhelm56,Møller Peter Rask5,Nielsen Einar Eg1

Affiliation:

1. Section for Marine Living Resources, National Institute of Aquatic Resources, Technical University of Denmark, Vejlsøvej 39, 8600 Silkeborg, Denmark

2. Matís ltd, Vínlandsleið 12, 113 Reykjavík, Iceland

3. TRACE Wildlife Forensics Network, 16 Corstorphine Hill Avenue, Edinburgh EH12 6LE, UK

4. Royal (Dick) School of Veterinary Studies and the Roslin Institute, University of Edinburgh, Easter Bush Campus, Edinburgh EH25 9RG, UK

5. Natural History Museum of Denmark, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen Ø, Denmark

6. NIVA Denmark Water Research, Njalsgade 76, 2300 Copenhagen S, Denmark

Abstract

Abstract Fisheries enforcement relies on visual catch identification and quantification at sea or when landed. Silage (fish dissolved in acid) and fish blocks (block frozen fish) are promising methods for on-board processing and storage of low-value catches. We examined the use of non-destructive sampling and two DNA-based methods, quantitative PCR (qPCR) and metabarcoding, to assess species composition and relative abundance in industrial grade experimental silage and fish blocks. We demonstrate the ability to identify and quantify DNA from fish species in both products. qPCR analysis of small silage samples collected over 21 days detected all target control species. DNA from one species (Atlantic wolffish) was consistently overrepresented while, for three species of gadoids (Atlantic cod, haddock and whiting), the DNA content matched input tissue proportions with high accuracy. qPCR and metabarcoding of fish blocks, sampled as run-off water and exterior swabs, provided consistent species detection, with the highest variance observed in quantification from swab samples. Our analysis shows that DNA-based methods have significant potential as a tool for species identification and quantification of complex on-board-processed seafood products and are readily applicable to taxonomically and morphologically similar fish. There is, however, a need for establishing DNA/weight calibration factors for primary fisheries species.

Funder

European Union’s Horizon 2020

Publisher

Oxford University Press (OUP)

Subject

Ecology,Aquatic Science,Ecology, Evolution, Behavior and Systematics,Oceanography

Reference38 articles.

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2. Development of a qPCR method for the identification and quantification of two closely related tuna species, Bigeye tuna (Thunnus obesus) and Yellowfin tuna (Thunnus albacares), in canned tuna;Bojolly;Journal of Agricultural and Food Chemistry,2017

3. The evolution of per-cell organelle number;Cole;Frontiers in Cell and Developmental Biology,2016

4. Long-range PCR allows sequencing of mitochondrial genomes from environmental DNA;Deiner;Methods in Ecology and Evolution,2017

5. European Commission. 2013. Regulation (EU) No 1380/2013 of the European Parliament and of the Council of 11 December 2013. Official Journal of the European Union. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32013R1380.

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