benthic communities bacterial in Antarctica and the arctic
Citation
Kleinteich J, Hildebrand F, Bahram M, Voigt A, Wood S, Jungblut A, Küpper F, Quesada A, Camacho A, Pearce D, Convey P, Vincent W, Zarfl C, Bork P, Dietrich D, Sweetlove M (2019). benthic communities bacterial in Antarctica and the arctic. Version 1.2. SCAR - Microbial Antarctic Resource System. Metadata dataset https://doi.org/10.15468/bqwxdt accessed via GBIF.org on 2024-11-22.Description
Amplicon sequencing dataset of benthic Bacteria (16S ssh rRNA gene) occurring in pools, streams and wet soils of (sub-)Arctic and (sub-)Antarctic regionsSampling Description
Study Extent
Samples from microbial communities growing on wet soil, in small streams and ponds were collected during several field campaigns (three in each of the Arctic, the Antarctic and non-polar regions) between 2007 and 2014.Sampling
Samples were collected in sterile tubes or bags using a sterile spatula or similar equipment. All samples were stored frozen (−20°C) or freeze-dried and stored frozen until further use.Method steps
- Microbial DNA was extracted from 0.05 to 0.1 g subsamples using the PowerSoil® DNA Isolation Kit (Qiagen, Germantown, USA) following the manufacturer's recommendations and DNA eluted in sterile DNAse-free water. The DNA quality and quantity was assessed using a NanoDrop (NanoDrop 3300 Fluorospectrometer, ThermoScientific). DNA extracts were stored frozen (−20°C) for no longer than three months before subsequent processing. Samples from Northern Canada were extracted as described in Jungblut et al. (2010), dried and stored frozen.
- DNA obtained from 90 environmental samples was amplified using primers targeting the V3-V4 region of the 16S rRNA gene (F319 5′-ACTCCTACGGGAGGCAGCAG-3′, R806 5′-GGACTACHVGGGTWTCTAAT-3′)., using a dual multiplexing approach and a “heterogeneity spacer” of 0–3 bp length between the Illumina adapter and the forward/reverse primer sequence to increase read quality. PCR was carried out according to the manual of the Q5 high-fidelity polymerase (New England BioLabs, Ipswich, USA) with a final primer concentration of 0.2 μM and an annealing temperature of 65°C for 15 cycles.
- The PCR product (1 μl) was used in the second PCR. This PCR was performed using the forward and barcoded reverse primers from the NEXTflex™ 16S V1-V3 Amplicon-Seq Kit (Bioo Scientific, Austin, Texas, USA) at final concentrations of 0.15 μM and an annealing temperature of 65°C for 25 cycles. The remaining PCR conditions were as indicated in manufacturer's instructions for the Q5 high-fidelity polymerase. PCR products were cleaned up with the Agencourt AMPure XP—PCR Purification system (Beckman Coulter, Brea, USA) according to the manufacturer's instructions, and multiplexed at equal concentration. Sequencing was performed using a 300 bp paired-end sequencing protocol on the Illumina MiSeq platform (Illumina, San Diego, USA) at the Genomics Core Facility, European Molecular Biology Laboratory, Heidelberg.
Taxonomic Coverages
Amplicon sequencing dataset of Bacteria 16S ssu rRNA gene
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Bacteriacommon name: Bacteria rank: domain
Geographic Coverages
pond, stream and wet soil samples from Sweden, Bulgaria, Antarctica, New Zealand, Canada and Svalbard
Bibliographic Citations
- Kleinteich, J., Hildebrand, F., Bahram, M., Voigt, A. Y., Wood, S. A., Jungblut, A. D., ... & Convey, P. (2017). Pole-to-pole connections: Similarities between Arctic and Antarctic microbiomes and their vulnerability to environmental change. Frontiers in Ecology and Evolution, 5, 137. -
Contacts
Julia Kleinteichoriginator
University of Tübingen
Tübingen
DE
Falk Hildebrand
originator
European Molecular Biology Laboratory
Heidelberg
DE
Mohammad Bahram
originator
Uppsala University
Uppsala
SE
email: Mohammad.Bahram@ebc.uu.se
Anita Voigt
originator
European Molecular Biology Laboratory
Heidelberg
DE
Susanna Wood
originator
Cawthron Institute
Nelson
NZ
Anne Jungblut
originator
London Natural History Museum
London
GB
Frithjof Küpper
originator
Scottish Association for Marine Science
Oban
GB
email: fkuepper@abdn.ac.uk
Antonio Quesada
originator
Autonomous University of Madrid
Madrid
ES
Antonio Camacho
originator
University of Valencia
Valencia
ES
David Pearce
originator
University of Northumbria at Newcastle
Newcastle
GB
Peter Convey
originator
British Antarctic Survey
Cambridge
GB
Warwick Vincent
originator
Université Laval
Quebec
CA
Christiane Zarfl
originator
University of Tübingen
Tübingen
DE
Peer Bork
originator
European Molecular Biology Laboratory
Heidelberg
DE
Daniel Dietrich
originator
University of Konstanz
Konstanz
DE
Maxime Sweetlove
metadata author
position: Research assistent
Royal Belgian Institute for Natural Sciences
Rue Vautier 29
Brussels
1000
email: msweetlove@naturalsciences.be
Julia Kleinteich
administrative point of contact
University of Tübingen
Tübingen
DE