High-throughput amplicon sequencing of rRNA genes requires a copy number correction to accurately reflect the effects of management practices on soil nematode community structure

dc.citation.doidoi:10.1111/mec.12480en_US
dc.citation.epage5471en_US
dc.citation.issue21en_US
dc.citation.jtitleMolecular Ecologyen_US
dc.citation.spage5456en_US
dc.citation.volume22en_US
dc.contributor.authorDarby, B. J.
dc.contributor.authorTodd, Timothy C.
dc.contributor.authorHerman, Michael A.
dc.contributor.authoreidnemaen_US
dc.contributor.authoreidmhermanen_US
dc.date.accessioned2014-06-12T20:16:14Z
dc.date.available2014-06-12T20:16:14Z
dc.date.issued2014-06-12
dc.date.published2013en_US
dc.description.abstractNematodes are abundant consumers in grassland soils, but more sensitive and specific methods of enumeration are needed to improve our understanding of how different nematode species affect, and are affected by, ecosystem processes. High‐throughput amplicon sequencing is used to enumerate microbial and invertebrate communities at a high level of taxonomic resolution, but the method requires validation against traditional specimen‐based morphological identifications. To investigate the consistency between these approaches, we enumerated nematodes from a 25‐year field experiment using both morphological and molecular identification techniques in order to determine the long‐term effects of annual burning and nitrogen enrichment on soil nematode communities. Family‐level frequencies based on amplicon‐sequencing were not initially consistent with specimen‐based counts, but correction for differences in rRNA gene copy number using a genetic algorithm improved quantitative accuracy. Multivariate analysis of corrected sequence‐based abundances of nematode families was consistent with, but not identical to, analysis of specimen‐based counts. In both cases, herbivores, fungivores, and predator/omnivores generally were more abundant in burned than non‐burned plots, while bacterivores generally were more abundant in non-burned or nitrogen enriched plots. Discriminate analysis of sequence‐based abundances identified putative indicator species representing each trophic group. We conclude that high-throughput amplicon sequencing can be a valuable method for characterizing nematode communities at high taxonomic resolution as long as rRNA gene copy number variation is accounted for and accurate sequence databases are available.en_US
dc.identifier.urihttp://hdl.handle.net/2097/17844
dc.language.isoen_USen_US
dc.relation.urihttp://onlinelibrary.wiley.com/doi/10.1111/mec.12480/abstracten_US
dc.rightsThis is the peer reviewed version of the following article: Darby, B. J., Todd, T. C., & Herman, M. A. (2013). High-throughput amplicon sequencing of rRNA genes requires a copy number correction to accurately reflect the effects of management practices on soil nematode community structure. Molecular Ecology, 22(21), 5456–5471, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1111/mec.12480/abstracten_US
dc.subjectTallgrass prairieen_US
dc.subjectNematodesen_US
dc.subjectKonza prairieen_US
dc.subjectBar‐codingen_US
dc.subjectNitrogen enrichmenten_US
dc.subjectBurningen_US
dc.titleHigh-throughput amplicon sequencing of rRNA genes requires a copy number correction to accurately reflect the effects of management practices on soil nematode community structureen_US
dc.typeArticle (author version)en_US

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