| Literature DB >> 31293086 |
Yinqiu Ji1, Tea Huotari2, Tomas Roslin2,3, Niels Martin Schmidt4,5, Jiaxin Wang1, Douglas W Yu1,6,7, Otso Ovaskainen8,9.
Abstract
The accurate quantification of eukaryotic species abundances from bulk samples remains a key challenge for community ecology and environmental biomonitoring. We resolve this challenge by combining shotgun sequencing, mapping to reference DNA barcodes or to mitogenomes, and three correction factors: (a) a percent-coverage threshold to filter out false positives, (b) an internal-standard DNA spike-in to correct for stochasticity during sequencing, and (c) technical replicates to correct for stochasticity across sequencing runs. The SPIKEPIPE pipeline achieves a strikingly high accuracy of intraspecific abundance estimates (in terms of DNA mass) from samples of known composition (mapping to barcodes R2 = .93, mitogenomes R2 = .95) and a high repeatability across environmental-sample replicates (barcodes R2 = .94, mitogenomes R2 = .93). As proof of concept, we sequence arthropod samples from the High Arctic, systematically collected over 17 years, detecting changes in species richness, species-specific abundances, and phenology. SPIKEPIPE provides cost-efficient and reliable quantification of eukaryotic communities.Keywords: Araneae; Arthropoda; COI internal standard; DNA barcoding; biomonitoring; community composition; insecta; metagenomics; mitogenomes; mitogenomics
Mesh:
Substances:
Year: 2019 PMID: 31293086 DOI: 10.1111/1755-0998.13057
Source DB: PubMed Journal: Mol Ecol Resour ISSN: 1755-098X Impact factor: 7.090