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Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities
Environmental DNA (eDNA) metabarcoding has been used increasingly to assess biodiversity of aquatic vertebrates. However, there still remains to be developed a sampling design of eDNA metabarcoding that can ensure high detection rates of species with minimum total survey effort, especially for large...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665893/ https://www.ncbi.nlm.nih.gov/pubmed/29093520 http://dx.doi.org/10.1038/s41598-017-14978-6 |
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author | Sato, Hirotoshi Sogo, Yuki Doi, Hideyuki Yamanaka, Hiroki |
author_facet | Sato, Hirotoshi Sogo, Yuki Doi, Hideyuki Yamanaka, Hiroki |
author_sort | Sato, Hirotoshi |
collection | PubMed |
description | Environmental DNA (eDNA) metabarcoding has been used increasingly to assess biodiversity of aquatic vertebrates. However, there still remains to be developed a sampling design of eDNA metabarcoding that can ensure high detection rates of species with minimum total survey effort, especially for large-scale surveys of aquatic organisms. We here tested whether pooling of eDNA samples can be used to evaluate biodiversity of freshwater fishes in four satellite lakes of Lake Biwa, Japan. Fish communities detected by eDNA metabarcoding of the mitochondrial 12S region were compared between the individual and pooled samples. In the individual samples, 31, 22, 33, and 31 fish lineages (proxies for species) were observed at the respective sites, within which moderate spatial autocorrelation existed. In the pooled samples, 30, 20, 29, and 27, lineages were detected, respectively, even after 15 PCR replicates. Lineages accounting for < 0.05% of the total read count of each site’s individual samples were mostly undetectable in the pooled samples. Moreover, fish communities detected were similar among PCR replicates in the pooled samples. Because of the decreased detection rates, the pooling strategy is unsuitable for estimating fish species richness. However, this procedure is useful potentially for among-site comparison of representative fish communities. |
format | Online Article Text |
id | pubmed-5665893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56658932017-11-08 Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities Sato, Hirotoshi Sogo, Yuki Doi, Hideyuki Yamanaka, Hiroki Sci Rep Article Environmental DNA (eDNA) metabarcoding has been used increasingly to assess biodiversity of aquatic vertebrates. However, there still remains to be developed a sampling design of eDNA metabarcoding that can ensure high detection rates of species with minimum total survey effort, especially for large-scale surveys of aquatic organisms. We here tested whether pooling of eDNA samples can be used to evaluate biodiversity of freshwater fishes in four satellite lakes of Lake Biwa, Japan. Fish communities detected by eDNA metabarcoding of the mitochondrial 12S region were compared between the individual and pooled samples. In the individual samples, 31, 22, 33, and 31 fish lineages (proxies for species) were observed at the respective sites, within which moderate spatial autocorrelation existed. In the pooled samples, 30, 20, 29, and 27, lineages were detected, respectively, even after 15 PCR replicates. Lineages accounting for < 0.05% of the total read count of each site’s individual samples were mostly undetectable in the pooled samples. Moreover, fish communities detected were similar among PCR replicates in the pooled samples. Because of the decreased detection rates, the pooling strategy is unsuitable for estimating fish species richness. However, this procedure is useful potentially for among-site comparison of representative fish communities. Nature Publishing Group UK 2017-11-01 /pmc/articles/PMC5665893/ /pubmed/29093520 http://dx.doi.org/10.1038/s41598-017-14978-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sato, Hirotoshi Sogo, Yuki Doi, Hideyuki Yamanaka, Hiroki Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title | Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title_full | Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title_fullStr | Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title_full_unstemmed | Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title_short | Usefulness and limitations of sample pooling for environmental DNA metabarcoding of freshwater fish communities |
title_sort | usefulness and limitations of sample pooling for environmental dna metabarcoding of freshwater fish communities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665893/ https://www.ncbi.nlm.nih.gov/pubmed/29093520 http://dx.doi.org/10.1038/s41598-017-14978-6 |
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