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Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding
Environmental DNA (eDNA) analysis is a novel approach for biomonitoring and has been mostly used in clear water. It is difficult to detect eDNA in turbid water as filter clogging occurs, and environmental samples contain various substances that inhibit the polymerase chain reaction (PCR) and affect...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104373/ https://www.ncbi.nlm.nih.gov/pubmed/33961651 http://dx.doi.org/10.1371/journal.pone.0250162 |
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author | Takasaki, Kazuto Aihara, Hiroki Imanaka, Takanobu Matsudaira, Takahiro Tsukahara, Keita Usui, Atsuko Osaki, Sora Doi, Hideyuki |
author_facet | Takasaki, Kazuto Aihara, Hiroki Imanaka, Takanobu Matsudaira, Takahiro Tsukahara, Keita Usui, Atsuko Osaki, Sora Doi, Hideyuki |
author_sort | Takasaki, Kazuto |
collection | PubMed |
description | Environmental DNA (eDNA) analysis is a novel approach for biomonitoring and has been mostly used in clear water. It is difficult to detect eDNA in turbid water as filter clogging occurs, and environmental samples contain various substances that inhibit the polymerase chain reaction (PCR) and affect the accuracy of eDNA analysis. Therefore, we applied a pre-filtration method to better detect the fish species (particularly pale chub, Opsariichthys platypus) present in a water body by measuring eDNA in environmental samples containing PCR inhibitors. Upon conducting 12S rRNA metabarcoding analysis (MiFish), we found that pre-filtration did not affect the number or identities of fish species detected in our samples, but pre-filtration through pore sizes resulted in significantly reduced variance among replicate samples. Additionally, PCR amplification was improved by the pre-filtration of environmental samples containing PCR inhibitors such as humic substances. Although this study may appear to be a conservative and ancillary experiment, pre-filtration is a simple technique that can not only improve the physical properties of water, such as turbidity, but also the quality of eDNA biomonitoring. |
format | Online Article Text |
id | pubmed-8104373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-81043732021-05-18 Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding Takasaki, Kazuto Aihara, Hiroki Imanaka, Takanobu Matsudaira, Takahiro Tsukahara, Keita Usui, Atsuko Osaki, Sora Doi, Hideyuki PLoS One Research Article Environmental DNA (eDNA) analysis is a novel approach for biomonitoring and has been mostly used in clear water. It is difficult to detect eDNA in turbid water as filter clogging occurs, and environmental samples contain various substances that inhibit the polymerase chain reaction (PCR) and affect the accuracy of eDNA analysis. Therefore, we applied a pre-filtration method to better detect the fish species (particularly pale chub, Opsariichthys platypus) present in a water body by measuring eDNA in environmental samples containing PCR inhibitors. Upon conducting 12S rRNA metabarcoding analysis (MiFish), we found that pre-filtration did not affect the number or identities of fish species detected in our samples, but pre-filtration through pore sizes resulted in significantly reduced variance among replicate samples. Additionally, PCR amplification was improved by the pre-filtration of environmental samples containing PCR inhibitors such as humic substances. Although this study may appear to be a conservative and ancillary experiment, pre-filtration is a simple technique that can not only improve the physical properties of water, such as turbidity, but also the quality of eDNA biomonitoring. Public Library of Science 2021-05-07 /pmc/articles/PMC8104373/ /pubmed/33961651 http://dx.doi.org/10.1371/journal.pone.0250162 Text en © 2021 Takasaki et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Takasaki, Kazuto Aihara, Hiroki Imanaka, Takanobu Matsudaira, Takahiro Tsukahara, Keita Usui, Atsuko Osaki, Sora Doi, Hideyuki Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title | Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title_full | Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title_fullStr | Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title_full_unstemmed | Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title_short | Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding |
title_sort | water pre-filtration methods to improve environmental dna detection by real-time pcr and metabarcoding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104373/ https://www.ncbi.nlm.nih.gov/pubmed/33961651 http://dx.doi.org/10.1371/journal.pone.0250162 |
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