2021
DOI: 10.1080/03014223.2020.1858880
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Detecting the pest fish,Gambusia affinisfrom environmental DNA in New Zealand: a comparison of methods

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Cited by 6 publications
(7 citation statements)
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“…While both qPCR and ddPCR have been found to produce either similar estimates of DNA concentrations (Nathan et al, 2014) or strong relationships between marker copy numbers and abundances (Wood et al, 2019b), most studies found ddPCR more sensitive than qPCR. This may be because in ddPCR each sample is partitioned into 15,000-20,000 microfluidic droplets (see above), where the amplification reaction occurs independently and concentrations of PCR inhibitors can be strongly reduced (Banks et al, 2021;Brys et al, 2021;Doi et al, 2015; (which was not certified by peer review) is the author/funder. All rights reserved.…”
Section: 4mentioning
confidence: 99%
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“…While both qPCR and ddPCR have been found to produce either similar estimates of DNA concentrations (Nathan et al, 2014) or strong relationships between marker copy numbers and abundances (Wood et al, 2019b), most studies found ddPCR more sensitive than qPCR. This may be because in ddPCR each sample is partitioned into 15,000-20,000 microfluidic droplets (see above), where the amplification reaction occurs independently and concentrations of PCR inhibitors can be strongly reduced (Banks et al, 2021;Brys et al, 2021;Doi et al, 2015; (which was not certified by peer review) is the author/funder. All rights reserved.…”
Section: 4mentioning
confidence: 99%
“…In this approach, sequences belonging to multiple species are obtained from complex environmental samples via HTS, using short regions of one or a few marker genes, which are targeted with broad-spectrum or group-specific primers (Deiner et al, 2017;Taberlet et al, 2012a). Comparisons between metabarcoding and targeted approaches indicated that qPCR or cPCR or ddPCR are more sensitive in the detection of single species or a small set of species, in particular when the target DNA occurs at low densities (Banks et al, 2021;Blackman et al, 2020Blackman et al, , 2018Harper et al, 2018a;Moss et al, 2022;Roy et al, 2018). For instance, qPCR was highly effective in detecting the invasive tunicate Didemnum vexillum Kott, 2002 from seawater eDNA, whereas metabarcoding was unable to recover it, even at locations where it is known to be present, but detected several other established invasive species (Gargan et al, 2022).…”
Section: 4mentioning
confidence: 99%
“…These filters were kept at room temperature until time of extraction. Smith-Root conducted a study showing that DNA did not degrade within 6 months at room temperature (Thomas et al, 2019) and these filters have also been used in other studies (Loeza-Quintana et al, 2020;Skinner et al, 2020;Banks et al, 2021;Nolan et al, 2022). These self-preserving eDNA filters are made of hydrophilic plastic which absorbs any remaining moisture into the package and preserves the DNA and prokaryotes via desiccation which has been shown as an effective preservation technique in other studies (Garcıá, 2011;Manzanera, 2021).…”
Section: Microbiome Analysesmentioning
confidence: 99%
“…Single-species detection using eDNA was one of the earlier established applications of this technology for vertebrate species. In particular, the use of eDNA in detecting invasive species has been particularly popular and Banks et al (2021) has demonstrated this applicability for the detection of Gambusia affinis. This study compared various workflows from collection of the sample through to the laboratory processes and how these impacted on the sensitivity of eDNA for detecting this invasive.…”
Section: Editorialmentioning
confidence: 99%