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Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats
Large carnivore feeding ecology plays a crucial role for management and conservation for predators and their prey. One of the keys to this kind of research is to identify the species composition in the predator diet, for example, prey determination from scat content. DNA‐based methods applied to det...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427573/ https://www.ncbi.nlm.nih.gov/pubmed/34522337 http://dx.doi.org/10.1002/ece3.7918 |
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author | Di Bernardi, Cecilia Wikenros, Camilla Hedmark, Eva Boitani, Luigi Ciucci, Paolo Sand, Håkan Åkesson, Mikael |
author_facet | Di Bernardi, Cecilia Wikenros, Camilla Hedmark, Eva Boitani, Luigi Ciucci, Paolo Sand, Håkan Åkesson, Mikael |
author_sort | Di Bernardi, Cecilia |
collection | PubMed |
description | Large carnivore feeding ecology plays a crucial role for management and conservation for predators and their prey. One of the keys to this kind of research is to identify the species composition in the predator diet, for example, prey determination from scat content. DNA‐based methods applied to detect prey in predators’ scats are viable alternatives to traditional macroscopic approaches, showing an increased reliability and higher prey detection rate. Here, we developed a molecular method for prey species identification in wolf (Canis lupus) scats using multiple species‐specific marker loci on the cytochrome b gene for 18 target species. The final panel consisted of 80 assays, with a minimum of four markers per target species, and that amplified specifically when using a high‐throughput Nanofluidic array technology (Fluidigm Inc.). As a practical example, we applied the method to identify target prey species DNA in 80 wolf scats collected in Sweden. Depending on the number of amplifying markers required to obtain a positive species call in a scat, the success in determining at least one prey species from the scats ranged from 44% to 92%. Although we highlight the need to evaluate the optimal number of markers for sensitive target species detection, the developed method is a fast and cost‐efficient tool for prey identification in wolf scats and it also has the potential to be further developed and applied to other areas and large carnivores as well. |
format | Online Article Text |
id | pubmed-8427573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84275732021-09-13 Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats Di Bernardi, Cecilia Wikenros, Camilla Hedmark, Eva Boitani, Luigi Ciucci, Paolo Sand, Håkan Åkesson, Mikael Ecol Evol Original Research Large carnivore feeding ecology plays a crucial role for management and conservation for predators and their prey. One of the keys to this kind of research is to identify the species composition in the predator diet, for example, prey determination from scat content. DNA‐based methods applied to detect prey in predators’ scats are viable alternatives to traditional macroscopic approaches, showing an increased reliability and higher prey detection rate. Here, we developed a molecular method for prey species identification in wolf (Canis lupus) scats using multiple species‐specific marker loci on the cytochrome b gene for 18 target species. The final panel consisted of 80 assays, with a minimum of four markers per target species, and that amplified specifically when using a high‐throughput Nanofluidic array technology (Fluidigm Inc.). As a practical example, we applied the method to identify target prey species DNA in 80 wolf scats collected in Sweden. Depending on the number of amplifying markers required to obtain a positive species call in a scat, the success in determining at least one prey species from the scats ranged from 44% to 92%. Although we highlight the need to evaluate the optimal number of markers for sensitive target species detection, the developed method is a fast and cost‐efficient tool for prey identification in wolf scats and it also has the potential to be further developed and applied to other areas and large carnivores as well. John Wiley and Sons Inc. 2021-08-01 /pmc/articles/PMC8427573/ /pubmed/34522337 http://dx.doi.org/10.1002/ece3.7918 Text en © 2021 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Di Bernardi, Cecilia Wikenros, Camilla Hedmark, Eva Boitani, Luigi Ciucci, Paolo Sand, Håkan Åkesson, Mikael Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title | Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title_full | Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title_fullStr | Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title_full_unstemmed | Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title_short | Multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey DNA from carnivore scats |
title_sort | multiple species‐specific molecular markers using nanofluidic array as a tool to detect prey dna from carnivore scats |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427573/ https://www.ncbi.nlm.nih.gov/pubmed/34522337 http://dx.doi.org/10.1002/ece3.7918 |
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