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Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA
Identifying species occupying an area is essential for many ecological and conservation studies. Faecal DNA is a potentially powerful method for identifying cryptic mammalian species. In New Zealand, 10 species of ungulate (Order: Artiodactyla) have established wild populations and are managed as pe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956866/ https://www.ncbi.nlm.nih.gov/pubmed/24637802 http://dx.doi.org/10.1371/journal.pone.0092043 |
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author | Ramón-Laca, Ana Gleeson, Dianne Yockney, Ivor Perry, Michael Nugent, Graham Forsyth, David M. |
author_facet | Ramón-Laca, Ana Gleeson, Dianne Yockney, Ivor Perry, Michael Nugent, Graham Forsyth, David M. |
author_sort | Ramón-Laca, Ana |
collection | PubMed |
description | Identifying species occupying an area is essential for many ecological and conservation studies. Faecal DNA is a potentially powerful method for identifying cryptic mammalian species. In New Zealand, 10 species of ungulate (Order: Artiodactyla) have established wild populations and are managed as pests because of their impacts on native ecosystems. However, identifying the ungulate species present within a management area based on pellet morphology is unreliable. We present a method that enables reliable identification of 10 ungulate species (red deer, sika deer, rusa deer, fallow deer, sambar deer, white-tailed deer, Himalayan tahr, Alpine chamois, feral sheep, and feral goat) from swabs of faecal pellets. A high resolution melting (HRM) assay, targeting a fragment of the 12S rRNA gene, was developed. Species-specific primers were designed and combined in a multiplex PCR resulting in fragments of different length and therefore different melting behaviour for each species. The method was developed using tissue from each of the 10 species, and was validated in blind trials. Our protocol enabled species to be determined for 94% of faecal pellet swabs collected during routine monitoring by the New Zealand Department of Conservation. Our HRM method enables high-throughput and cost-effective species identification from low DNA template samples, and could readily be adapted to discriminate other mammalian species from faecal DNA. |
format | Online Article Text |
id | pubmed-3956866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39568662014-03-18 Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA Ramón-Laca, Ana Gleeson, Dianne Yockney, Ivor Perry, Michael Nugent, Graham Forsyth, David M. PLoS One Research Article Identifying species occupying an area is essential for many ecological and conservation studies. Faecal DNA is a potentially powerful method for identifying cryptic mammalian species. In New Zealand, 10 species of ungulate (Order: Artiodactyla) have established wild populations and are managed as pests because of their impacts on native ecosystems. However, identifying the ungulate species present within a management area based on pellet morphology is unreliable. We present a method that enables reliable identification of 10 ungulate species (red deer, sika deer, rusa deer, fallow deer, sambar deer, white-tailed deer, Himalayan tahr, Alpine chamois, feral sheep, and feral goat) from swabs of faecal pellets. A high resolution melting (HRM) assay, targeting a fragment of the 12S rRNA gene, was developed. Species-specific primers were designed and combined in a multiplex PCR resulting in fragments of different length and therefore different melting behaviour for each species. The method was developed using tissue from each of the 10 species, and was validated in blind trials. Our protocol enabled species to be determined for 94% of faecal pellet swabs collected during routine monitoring by the New Zealand Department of Conservation. Our HRM method enables high-throughput and cost-effective species identification from low DNA template samples, and could readily be adapted to discriminate other mammalian species from faecal DNA. Public Library of Science 2014-03-17 /pmc/articles/PMC3956866/ /pubmed/24637802 http://dx.doi.org/10.1371/journal.pone.0092043 Text en © 2014 Ramón-Laca et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ramón-Laca, Ana Gleeson, Dianne Yockney, Ivor Perry, Michael Nugent, Graham Forsyth, David M. Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title | Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title_full | Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title_fullStr | Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title_full_unstemmed | Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title_short | Reliable Discrimination of 10 Ungulate Species Using High Resolution Melting Analysis of Faecal DNA |
title_sort | reliable discrimination of 10 ungulate species using high resolution melting analysis of faecal dna |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956866/ https://www.ncbi.nlm.nih.gov/pubmed/24637802 http://dx.doi.org/10.1371/journal.pone.0092043 |
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