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Comparison of materials for rapid passive collection of environmental DNA

Passive collection is an emerging sampling method for environmental DNA (eDNA) in aquatic systems. Passive eDNA collection is inexpensive and efficient, and requires minimal equipment, making it suited to high‐density sampling and remote deployment. Here, we compare the effectiveness of nine membran...

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Autores principales: Bessey, Cindy, Gao, Yuan, Truong, Yen Bach, Miller, Haylea, Jarman, Simon Neil, Berry, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544503/
https://www.ncbi.nlm.nih.gov/pubmed/35570323
http://dx.doi.org/10.1111/1755-0998.13640
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author Bessey, Cindy
Gao, Yuan
Truong, Yen Bach
Miller, Haylea
Jarman, Simon Neil
Berry, Oliver
author_facet Bessey, Cindy
Gao, Yuan
Truong, Yen Bach
Miller, Haylea
Jarman, Simon Neil
Berry, Oliver
author_sort Bessey, Cindy
collection PubMed
description Passive collection is an emerging sampling method for environmental DNA (eDNA) in aquatic systems. Passive eDNA collection is inexpensive and efficient, and requires minimal equipment, making it suited to high‐density sampling and remote deployment. Here, we compare the effectiveness of nine membrane materials for passively collecting fish eDNA from a 3‐million‐litre marine mesocosm. We submerged materials (cellulose, cellulose with 1% and 3% chitosan, cellulose overlayed with electrospun nanofibres and 1% chitosan, cotton fibres, hemp fibres, and sponge with either zeolite or active carbon) for intervals between 5 and 1080 min. We show that for most materials, with as little as 5 min of submersion, mitochondrial fish eDNA measured with qPCR, and fish species richness measured with metabarcoding, was comparable to that collected by conventional filtering. Furthermore, PCR template DNA concentrations and species richness were generally not improved significantly by longer submersion. Species richness detected for all materials ranged between 11 and 37 species, with a median of 27, which was comparable to the range for filtered eDNA (19–32). Using scanning electron microscopy, we visualized biological matter adhering to the surface of materials, rather than entrapped, with images also revealing a diversity in size and structure of putative eDNA particles. eDNA can be collected rapidly from seawater with a passive approach and using a variety of materials. This will suit cost‐ and time‐sensitive biological surveys, and where access to equipment is limited.
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spelling pubmed-95445032022-10-14 Comparison of materials for rapid passive collection of environmental DNA Bessey, Cindy Gao, Yuan Truong, Yen Bach Miller, Haylea Jarman, Simon Neil Berry, Oliver Mol Ecol Resour RESOURCE ARTICLES Passive collection is an emerging sampling method for environmental DNA (eDNA) in aquatic systems. Passive eDNA collection is inexpensive and efficient, and requires minimal equipment, making it suited to high‐density sampling and remote deployment. Here, we compare the effectiveness of nine membrane materials for passively collecting fish eDNA from a 3‐million‐litre marine mesocosm. We submerged materials (cellulose, cellulose with 1% and 3% chitosan, cellulose overlayed with electrospun nanofibres and 1% chitosan, cotton fibres, hemp fibres, and sponge with either zeolite or active carbon) for intervals between 5 and 1080 min. We show that for most materials, with as little as 5 min of submersion, mitochondrial fish eDNA measured with qPCR, and fish species richness measured with metabarcoding, was comparable to that collected by conventional filtering. Furthermore, PCR template DNA concentrations and species richness were generally not improved significantly by longer submersion. Species richness detected for all materials ranged between 11 and 37 species, with a median of 27, which was comparable to the range for filtered eDNA (19–32). Using scanning electron microscopy, we visualized biological matter adhering to the surface of materials, rather than entrapped, with images also revealing a diversity in size and structure of putative eDNA particles. eDNA can be collected rapidly from seawater with a passive approach and using a variety of materials. This will suit cost‐ and time‐sensitive biological surveys, and where access to equipment is limited. John Wiley and Sons Inc. 2022-06-01 2022-10 /pmc/articles/PMC9544503/ /pubmed/35570323 http://dx.doi.org/10.1111/1755-0998.13640 Text en © 2022 The Authors. Molecular Ecology Resources published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle RESOURCE ARTICLES
Bessey, Cindy
Gao, Yuan
Truong, Yen Bach
Miller, Haylea
Jarman, Simon Neil
Berry, Oliver
Comparison of materials for rapid passive collection of environmental DNA
title Comparison of materials for rapid passive collection of environmental DNA
title_full Comparison of materials for rapid passive collection of environmental DNA
title_fullStr Comparison of materials for rapid passive collection of environmental DNA
title_full_unstemmed Comparison of materials for rapid passive collection of environmental DNA
title_short Comparison of materials for rapid passive collection of environmental DNA
title_sort comparison of materials for rapid passive collection of environmental dna
topic RESOURCE ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9544503/
https://www.ncbi.nlm.nih.gov/pubmed/35570323
http://dx.doi.org/10.1111/1755-0998.13640
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