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High-throughput sequencing of nematode communities from total soil DNA extractions
BACKGROUND: Nematodes are extremely diverse and numbers of species are predicted to be more than a million. Studies on nematode diversity are difficult and laborious using classical methods and therefore high-throughput sequencing is an attractive alternative. Primers that have been used in previous...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331302/ https://www.ncbi.nlm.nih.gov/pubmed/25880249 http://dx.doi.org/10.1186/s12898-014-0034-4 |
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author | Sapkota, Rumakanta Nicolaisen, Mogens |
author_facet | Sapkota, Rumakanta Nicolaisen, Mogens |
author_sort | Sapkota, Rumakanta |
collection | PubMed |
description | BACKGROUND: Nematodes are extremely diverse and numbers of species are predicted to be more than a million. Studies on nematode diversity are difficult and laborious using classical methods and therefore high-throughput sequencing is an attractive alternative. Primers that have been used in previous sequence-based studies are not nematode specific but also amplify other groups of organisms such as fungi and plantae, and thus require a nematode enrichment step that may introduce biases. RESULTS: In this study an amplification strategy which selectively amplifies a fragment of the SSU from nematodes without the need for enrichment was developed. Using this strategy on DNA templates from a set of 22 agricultural soils, we obtained 64.4% sequences of nematode origin in total, whereas the remaining sequences were almost entirely from other metazoans. The nematode sequences were derived from a broad taxonomic range and most sequences were from nematode taxa that have previously been found to be abundant in soil such as Tylenchida, Rhabditida, Dorylaimida, Triplonchida and Araeolaimida. CONCLUSIONS: Our amplification and sequencing strategy for assessing nematode diversity was able to collect a broad diversity without prior nematode enrichment and thus the method will be highly valuable in ecological studies of nematodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12898-014-0034-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4331302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43313022015-02-19 High-throughput sequencing of nematode communities from total soil DNA extractions Sapkota, Rumakanta Nicolaisen, Mogens BMC Ecol Methodology Article BACKGROUND: Nematodes are extremely diverse and numbers of species are predicted to be more than a million. Studies on nematode diversity are difficult and laborious using classical methods and therefore high-throughput sequencing is an attractive alternative. Primers that have been used in previous sequence-based studies are not nematode specific but also amplify other groups of organisms such as fungi and plantae, and thus require a nematode enrichment step that may introduce biases. RESULTS: In this study an amplification strategy which selectively amplifies a fragment of the SSU from nematodes without the need for enrichment was developed. Using this strategy on DNA templates from a set of 22 agricultural soils, we obtained 64.4% sequences of nematode origin in total, whereas the remaining sequences were almost entirely from other metazoans. The nematode sequences were derived from a broad taxonomic range and most sequences were from nematode taxa that have previously been found to be abundant in soil such as Tylenchida, Rhabditida, Dorylaimida, Triplonchida and Araeolaimida. CONCLUSIONS: Our amplification and sequencing strategy for assessing nematode diversity was able to collect a broad diversity without prior nematode enrichment and thus the method will be highly valuable in ecological studies of nematodes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12898-014-0034-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-12 /pmc/articles/PMC4331302/ /pubmed/25880249 http://dx.doi.org/10.1186/s12898-014-0034-4 Text en © Sapkota and Nicolaisen; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Sapkota, Rumakanta Nicolaisen, Mogens High-throughput sequencing of nematode communities from total soil DNA extractions |
title | High-throughput sequencing of nematode communities from total soil DNA extractions |
title_full | High-throughput sequencing of nematode communities from total soil DNA extractions |
title_fullStr | High-throughput sequencing of nematode communities from total soil DNA extractions |
title_full_unstemmed | High-throughput sequencing of nematode communities from total soil DNA extractions |
title_short | High-throughput sequencing of nematode communities from total soil DNA extractions |
title_sort | high-throughput sequencing of nematode communities from total soil dna extractions |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331302/ https://www.ncbi.nlm.nih.gov/pubmed/25880249 http://dx.doi.org/10.1186/s12898-014-0034-4 |
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