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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9544503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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
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title_full | Comparison of materials for rapid passive collection of environmental DNA
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title_fullStr | Comparison of materials for rapid passive collection of environmental DNA
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title_full_unstemmed | Comparison of materials for rapid passive collection of environmental DNA
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title_short | Comparison of materials for rapid passive collection of environmental DNA
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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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