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dc.contributor.authorIwaszkiewicz-Eggebrecht, Elzbieta
dc.contributor.authorGranqvist, Emma
dc.contributor.authorBuczek, Mateusz
dc.contributor.authorPrus, Monika
dc.contributor.authorKudlicka, Jan
dc.contributor.authorRoslin, Tomas
dc.contributor.authorTack, Ayco J. M.
dc.contributor.authorAndersson, Anders F.
dc.contributor.authorMiraldo, Andreia
dc.contributor.authorRonquist, Fredrik
dc.contributor.authorŁukasik, Piotr
dc.date.accessioned2023-07-18T07:18:20Z
dc.date.available2023-07-18T07:18:20Z
dc.date.created2023-05-08T15:05:56Z
dc.date.issued2023
dc.identifier.citationMethods in Ecology and Evolution. 2023, 14 (4), 1130-1146.en_US
dc.identifier.issn2041-210X
dc.identifier.urihttps://hdl.handle.net/11250/3079669
dc.description.abstractMetabarcoding (high-throughput sequencing of marker gene amplicons) has emerged as a promising and cost-effective method for characterizing insect community samples. Yet, the methodology varies greatly among studies and its performance has not been systematically evaluated to date. In particular, it is unclear how accurately metabarcoding can resolve species communities in terms of presence-absence, abundance and biomass. Here we use mock community experiments and a simple probabilistic model to evaluate the effect of different DNA extraction protocols on metabarcoding performance. Specifically, we ask four questions: (Q1) How consistent are the recovered community profiles across replicate mock communities?; (Q2) How does the choice of lysis buffer affect the recovery of the original community?; (Q3) How are community estimates affected by differing lysis times and homogenization? and (Q4) Is it possible to obtain adequate species abundance estimates through the use of biological spike-ins? We show that estimates are quite variable across community replicates. In general, a mild lysis protocol is better at reconstructing species lists and approximate counts, while homogenization is better at retrieving biomass composition. Small insects are more likely to be detected in lysates, while some tough species require homogenization to be detected. Results are less consistent across biological replicates for lysates than for homogenates. Some species are associated with strong PCR amplification bias, which complicates the reconstruction of species counts. Yet, with adequate spike-in data, species abundance can be determined with roughly 40% standard error for homogenates, and with roughly 50% standard error for lysates, under ideal conditions. In the latter case, however, this often requires species-specific reference data, while spike-in data generalize better across species for homogenates. We conclude that a non-destructive, mild lysis approach shows the highest promise for the presence/absence description of the community, while also allowing future morphological or molecular work on the material. However, homogenization protocols perform better for characterizing community composition, in particular in terms of biomass.en_US
dc.language.isoengen_US
dc.publisherBritish Ecological Societyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectabundance estimationen_US
dc.subjecthomogenizationen_US
dc.subjectMalaise trapen_US
dc.subjectmetabarcodingen_US
dc.subjectmock communitiesen_US
dc.subjectnon- destructive mild lysisen_US
dc.subjectspike-insen_US
dc.titleOptimizing insect metabarcoding using replicated mock communitiesen_US
dc.title.alternativeOptimizing insect metabarcoding using replicated mock communitiesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1130-1146en_US
dc.source.volume14en_US
dc.source.journalMethods in Ecology and Evolutionen_US
dc.source.issue4en_US
dc.identifier.doi10.1111/2041-210X.14073
dc.identifier.cristin2146224
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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