GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.

Here we describe GoFish, a strategy for single-species environmental DNA (eDNA) presence/absence assays using nested PCR. The assays amplify a mitochondrial 12S rDNA segment with vertebrate metabarcoding primers, followed by nested PCR with M13-tailed, species-specific primers. Sanger sequencing con...

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Main Authors: Mark Y Stoeckle, Mithun Das Mishu, Zachary Charlop-Powers
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0198717
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spelling doaj-741db599363143b2bc61f823fe8550aa2021-03-03T21:03:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011312e019871710.1371/journal.pone.0198717GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.Mark Y StoeckleMithun Das MishuZachary Charlop-PowersHere we describe GoFish, a strategy for single-species environmental DNA (eDNA) presence/absence assays using nested PCR. The assays amplify a mitochondrial 12S rDNA segment with vertebrate metabarcoding primers, followed by nested PCR with M13-tailed, species-specific primers. Sanger sequencing confirms positives detected by gel electrophoresis. We first obtained 12S sequences from 77 fish specimens for 36 northwestern Atlantic taxa not well documented in GenBank. Using these and existing 12S records, we designed GoFish assays for 11 bony fish species common in the lower Hudson River estuary and tested seasonal abundance and habitat preference at two sites. Additional assays detected nine cartilaginous fish species and a marine mammal, bottlenose dolphin, in southern New York Bight. GoFish sensitivity was equivalent to Illumina MiSeq metabarcoding. Unlike quantitative PCR (qPCR), GoFish does not require tissues of target and related species for assay development and a basic thermal cycler is sufficient. Unlike Illumina metabarcoding, indexing and batching samples are unnecessary and advanced bioinformatics expertise is not needed. From water collection to Sanger sequencing results, the assay can be carried out in three days. The main limitations to this approach, which employs metabarcoding primers, are the same as for metabarcoding, namely, inability to distinguish species with shared target sequences and inconsistent amplification of rarer eDNA. In addition, the performance of the 20 assays reported here as compared to other single-species eDNA assays is not known. This approach will be a useful addition to current eDNA methods when analyzing presence/absence of known species, when turnaround time is important, and in educational settings.https://doi.org/10.1371/journal.pone.0198717
collection DOAJ
language English
format Article
sources DOAJ
author Mark Y Stoeckle
Mithun Das Mishu
Zachary Charlop-Powers
spellingShingle Mark Y Stoeckle
Mithun Das Mishu
Zachary Charlop-Powers
GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
PLoS ONE
author_facet Mark Y Stoeckle
Mithun Das Mishu
Zachary Charlop-Powers
author_sort Mark Y Stoeckle
title GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
title_short GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
title_full GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
title_fullStr GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
title_full_unstemmed GoFish: A versatile nested PCR strategy for environmental DNA assays for marine vertebrates.
title_sort gofish: a versatile nested pcr strategy for environmental dna assays for marine vertebrates.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Here we describe GoFish, a strategy for single-species environmental DNA (eDNA) presence/absence assays using nested PCR. The assays amplify a mitochondrial 12S rDNA segment with vertebrate metabarcoding primers, followed by nested PCR with M13-tailed, species-specific primers. Sanger sequencing confirms positives detected by gel electrophoresis. We first obtained 12S sequences from 77 fish specimens for 36 northwestern Atlantic taxa not well documented in GenBank. Using these and existing 12S records, we designed GoFish assays for 11 bony fish species common in the lower Hudson River estuary and tested seasonal abundance and habitat preference at two sites. Additional assays detected nine cartilaginous fish species and a marine mammal, bottlenose dolphin, in southern New York Bight. GoFish sensitivity was equivalent to Illumina MiSeq metabarcoding. Unlike quantitative PCR (qPCR), GoFish does not require tissues of target and related species for assay development and a basic thermal cycler is sufficient. Unlike Illumina metabarcoding, indexing and batching samples are unnecessary and advanced bioinformatics expertise is not needed. From water collection to Sanger sequencing results, the assay can be carried out in three days. The main limitations to this approach, which employs metabarcoding primers, are the same as for metabarcoding, namely, inability to distinguish species with shared target sequences and inconsistent amplification of rarer eDNA. In addition, the performance of the 20 assays reported here as compared to other single-species eDNA assays is not known. This approach will be a useful addition to current eDNA methods when analyzing presence/absence of known species, when turnaround time is important, and in educational settings.
url https://doi.org/10.1371/journal.pone.0198717
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