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A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK

Segmentina nitida Müller 1774 is a freshwater snail which was formerly widespread throughout England and south Wales. Since the 1840s it has seen a rapid decline in its range which has been attributed to deteriorating water quality due to nutrient enrichment, lowering of water tables and over-manage...

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Autores principales: Rees, Helen C., Cousins, Mags E., Baker, Claire A., Maddison, Ben C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651049/
https://www.ncbi.nlm.nih.gov/pubmed/37967121
http://dx.doi.org/10.1371/journal.pone.0288267
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author Rees, Helen C.
Cousins, Mags E.
Baker, Claire A.
Maddison, Ben C.
author_facet Rees, Helen C.
Cousins, Mags E.
Baker, Claire A.
Maddison, Ben C.
author_sort Rees, Helen C.
collection PubMed
description Segmentina nitida Müller 1774 is a freshwater snail which was formerly widespread throughout England and south Wales. Since the 1840s it has seen a rapid decline in its range which has been attributed to deteriorating water quality due to nutrient enrichment, lowering of water tables and over-management of the ditches in which it resides. S. nitida has therefore been identified as a UK Biodiversity Action Plan (UKBAP) priority species which recommends further research for its conservation. Here we have developed a Taqman based qPCR eDNA assay for the detection of S. nitida at the Stodmarsh National Nature Reserve and compared the results with a manual survey of the ditches at this location. 32 ditches were surveyed in November 2020 (22 at Stodmarsh) and February 2021 (10 outside the known range of S.nitida). Our eDNA analysis exhibited an observed percentage agreement of 84% with a kappa coefficient of agreement between manual and eDNA surveys of 0.56 (95% CI 0.22 to 0.92). Three ditches determined to be negative for S. nitida by eDNA analysis were manual survey positive, and a further two ditches that were negative by manual survey were positive by eDNA analysis revealing the potential for improved overall detection rates using a combination of manual and eDNA methodologies. eDNA analysis could therefore augment manual survey techniques for S. nitida as a relatively quick and inexpensive tool for collecting presence and distribution data that could be used to inform manual surveys and management of ditches.
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spelling pubmed-106510492023-11-15 A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK Rees, Helen C. Cousins, Mags E. Baker, Claire A. Maddison, Ben C. PLoS One Research Article Segmentina nitida Müller 1774 is a freshwater snail which was formerly widespread throughout England and south Wales. Since the 1840s it has seen a rapid decline in its range which has been attributed to deteriorating water quality due to nutrient enrichment, lowering of water tables and over-management of the ditches in which it resides. S. nitida has therefore been identified as a UK Biodiversity Action Plan (UKBAP) priority species which recommends further research for its conservation. Here we have developed a Taqman based qPCR eDNA assay for the detection of S. nitida at the Stodmarsh National Nature Reserve and compared the results with a manual survey of the ditches at this location. 32 ditches were surveyed in November 2020 (22 at Stodmarsh) and February 2021 (10 outside the known range of S.nitida). Our eDNA analysis exhibited an observed percentage agreement of 84% with a kappa coefficient of agreement between manual and eDNA surveys of 0.56 (95% CI 0.22 to 0.92). Three ditches determined to be negative for S. nitida by eDNA analysis were manual survey positive, and a further two ditches that were negative by manual survey were positive by eDNA analysis revealing the potential for improved overall detection rates using a combination of manual and eDNA methodologies. eDNA analysis could therefore augment manual survey techniques for S. nitida as a relatively quick and inexpensive tool for collecting presence and distribution data that could be used to inform manual surveys and management of ditches. Public Library of Science 2023-11-15 /pmc/articles/PMC10651049/ /pubmed/37967121 http://dx.doi.org/10.1371/journal.pone.0288267 Text en © 2023 Rees 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
Rees, Helen C.
Cousins, Mags E.
Baker, Claire A.
Maddison, Ben C.
A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title_full A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title_fullStr A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title_full_unstemmed A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title_short A qPCR assay for the rapid and specific detection of Shining ram’s-horn snail (Segmentina nitida) eDNA from Stodmarsh National Nature Reserve, UK
title_sort qpcr assay for the rapid and specific detection of shining ram’s-horn snail (segmentina nitida) edna from stodmarsh national nature reserve, uk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651049/
https://www.ncbi.nlm.nih.gov/pubmed/37967121
http://dx.doi.org/10.1371/journal.pone.0288267
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