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New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla
Freshwater eels of the genus Anguilla comprise 16 species that include three subspecies and are characterized by their unique catadromous life cycles. Their life histories and nocturnal life styles make it difficult to observe them in freshwater and marine habitats. To investigate their distribution...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538671/ https://www.ncbi.nlm.nih.gov/pubmed/31138865 http://dx.doi.org/10.1038/s41598-019-44402-0 |
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author | Takeuchi, Aya Sado, Tetsuya Gotoh, Ryo O. Watanabe, Shun Tsukamoto, Katsumi Miya, Masaki |
author_facet | Takeuchi, Aya Sado, Tetsuya Gotoh, Ryo O. Watanabe, Shun Tsukamoto, Katsumi Miya, Masaki |
author_sort | Takeuchi, Aya |
collection | PubMed |
description | Freshwater eels of the genus Anguilla comprise 16 species that include three subspecies and are characterized by their unique catadromous life cycles. Their life histories and nocturnal life styles make it difficult to observe them in freshwater and marine habitats. To investigate their distribution and ecology in aquatic environments, we developed new PCR primers for metabarcoding environmental DNA (eDNA) from Anguilla. The new primers (MiEel) were designed for two conserved regions of the mitochondrial ATP6 gene, which amplify a variable region with sufficient interspecific variations ranging from five to 22 nucleotide differences (one to three nucleotide differences between three subspecies pairs). We confirmed the versatility of the MiEel primers for all freshwater eels using tissue DNA extracts when analyzed separately. The metabarcoding combined with the MiEel primers using mock communities enabled simultaneous detection of Anguilla at the species level. Analysis of eDNA samples from aquarium tanks, a controlled pond and natural rivers demonstrated that the MiEel metabarcoding could successfully detect the correct Anguilla species from water samples. These results suggested that eDNA metabarcoding with MiEel primers would be useful for non-invasively monitoring the presence of the endangered anguillid eels in aquatic environments where sampling surveys are difficult. |
format | Online Article Text |
id | pubmed-6538671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65386712019-06-07 New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla Takeuchi, Aya Sado, Tetsuya Gotoh, Ryo O. Watanabe, Shun Tsukamoto, Katsumi Miya, Masaki Sci Rep Article Freshwater eels of the genus Anguilla comprise 16 species that include three subspecies and are characterized by their unique catadromous life cycles. Their life histories and nocturnal life styles make it difficult to observe them in freshwater and marine habitats. To investigate their distribution and ecology in aquatic environments, we developed new PCR primers for metabarcoding environmental DNA (eDNA) from Anguilla. The new primers (MiEel) were designed for two conserved regions of the mitochondrial ATP6 gene, which amplify a variable region with sufficient interspecific variations ranging from five to 22 nucleotide differences (one to three nucleotide differences between three subspecies pairs). We confirmed the versatility of the MiEel primers for all freshwater eels using tissue DNA extracts when analyzed separately. The metabarcoding combined with the MiEel primers using mock communities enabled simultaneous detection of Anguilla at the species level. Analysis of eDNA samples from aquarium tanks, a controlled pond and natural rivers demonstrated that the MiEel metabarcoding could successfully detect the correct Anguilla species from water samples. These results suggested that eDNA metabarcoding with MiEel primers would be useful for non-invasively monitoring the presence of the endangered anguillid eels in aquatic environments where sampling surveys are difficult. Nature Publishing Group UK 2019-05-28 /pmc/articles/PMC6538671/ /pubmed/31138865 http://dx.doi.org/10.1038/s41598-019-44402-0 Text en © The Author(s) 2019 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 Takeuchi, Aya Sado, Tetsuya Gotoh, Ryo O. Watanabe, Shun Tsukamoto, Katsumi Miya, Masaki New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title | New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title_full | New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title_fullStr | New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title_full_unstemmed | New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title_short | New PCR primers for metabarcoding environmental DNA from freshwater eels, genus Anguilla |
title_sort | new pcr primers for metabarcoding environmental dna from freshwater eels, genus anguilla |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538671/ https://www.ncbi.nlm.nih.gov/pubmed/31138865 http://dx.doi.org/10.1038/s41598-019-44402-0 |
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