Microbial diversity (Bacteria and Archaea 16S rRNA gene) in geothermal sites of Deception Island volcano, Antarctica
Citation
Bendia A, Signori C, Franco D, Duarte R, Bohannan B, Pellizari V, Sweetlove M (2019). Microbial diversity (Bacteria and Archaea 16S rRNA gene) in geothermal sites of Deception Island volcano, Antarctica. Version 1.1. SCAR - Microbial Antarctic Resource System. Metadata dataset https://doi.org/10.15468/fbdsva accessed via GBIF.org on 2024-09-01.Description
Amplicon sequencing dataset (Illumina MiSeq) of Bacterial and Archaea microbial diversity (based on the 16S ssu rRNA gene) in surface sediment samples, taken along a temperature gradient (three points, each with three replicates) on two different geothermal active sites (+-10km apart) on Deception Island, Antarctica.Sampling Description
Study Extent
Sampling was performed on Deception Island (62°58′ S, 60°39′ W) during the XXXII Brazilian Antarctic Expedition (December 2013–January 2014), with logistical support from the polar vessel Npo. Almirante Maximiano. Surface sediment samples (ca. 5 cm) were collected in fumaroles and glaciers at the geothermally active sites of Fumarole Bay (62°58′02.7′′ S, 60°42′36.4′′ W) and Whalers Bay (62°58′45.1′′ S, 60°33′27.3′′ W).Sampling
In each site, three sediment samples were collected in each of three points with distinct temperatures: Points A and B were defined as samples collected in fumaroles, while point C was glacier samples, collected below the glacier’s edge. Distances between fumaroles and glaciers at each site were approximately 15 m, and the Whalers Bay and Fumarole Bay transects were approximately 10 km apart. All fumaroles were in the intertidal zone, with exception of point B from FB, which was in the subtidal (submerged at 50 cm depth in water column). Samples were stored at -20°C until arrival at the University of São Paulo, Brazil, in April 2014.Method steps
- Total genomic DNA was extracted from 10 g of sediment using a PowerMax Soil DNA Kit (MoBio, United States), according to the manufacturer’s protocol. Extracted DNA was concentrated and purified with PCR OneStep Inhibitor Removal Kit (Zymo Research, United States), and further quantified using Qubit dsDNA HS Assay (Thermo-Fisher Scientific, United States) and Qubit Fluorimeter 1.0 (Thermo-Fisher Scientific, United States). Microbial 16S rRNA gene fragments were amplified using the primers S-D-Bact-0341-b-S-17 and S-D-Bact-0785-a-A-21 for Bacteria, and S-D-Arch-0519-a-S-15 and S-D-Arch-1041-a-A-18 for Archaea (Klindworth et al., 2013), targeting the V3–V4 regions of the gene. The first PCR reaction was carried out with a thermal cycler (Thermo-Fisher Scientific, United States), using 25 μL of KAPA HiFi HotStart Ready Mix (KAPA Biosystems) polymerase, 5 ng of DNA, and 0.2 μM of each primer, under the following conditions: 95°C for 3 min, 30 cycles of 95°C for 30 s, 55 or 67°C for 30 s (for Bacteria and Archaea, respectively), 72°C for 30 s, and a final extension of 72°C for 5 min. After purification (QIAquick Gel Extraction Kit – QIAGEN, United States) and quantification, 50 ng of amplicons was amplified and used for library preparation, under the following conditions: 95°C for 3 min, eight cycles of 95°C for 30 s, 55 and 72°C for 30 s, and 72°C for 5 min. The libraries were purified using an AMPure XP beads kit (Beckman Coulter, United States).
- After quality checking (Bioanalyzer 2100, Agilent Technologies, United States), the amplicons from each sample were mixed at equimolar concentrations and then sequenced using the Illumina Miseq platform at the Facilities Center for Research Support (CEFAP, Institute of Biomedical Sciences, University of São Paulo).
Taxonomic Coverages
Bacteria (v3-v4 of the 16S ssu rRNA, targeted with the primer pair S-D-Bact-0341-b-S-17 and S-D-Bact-0785-a-A-21) and Archaea (v3-v4 of the 16S ssu rRNA, targeted with the primer pair S-D-Arch-0519-a-S-15 and S-D-Arch-1041-a-A-18)
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Bacteriacommon name: Bacteria rank: domain
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Archaeacommon name: Archaea rank: domain
Geographic Coverages
Geothermal anomalies at Fumarole Bay and Whalers Bay, Deception Island, Antarctica
Bibliographic Citations
- Bendia, A. G., Signori, C. N., Franco, D. C., Duarte, R. T., Bohannan, B. J., & Pellizari, V. H. (2018). A Mosaic of Geothermal and Marine Features Shapes Microbial Community Structure on Deception Island Volcano, Antarctica. Frontiers in Microbiology, 9. -
Contacts
Amanda Bendiaoriginator
Universidade de São Paulo
São Paulo
BR
Camila Signori
originator
Universidade de São Paulo
São Paulo
BR
Diego Franco
originator
Universidade de São Paulo
São Paulo
BR
Rubens Duarte
originator
Universidade de São Paulo
São Paulo
BR
Brendan Bohannan
originator
University of Oregon
Eugene
US
Vivian Pellizari
originator
Universidade de São Paulo
São Paulo
BR
Maxime Sweetlove
metadata author
position: Research assistent
Royal Belgian Institute for Natural Sciences
Rue Vautier 29
Brussels
1000
email: msweetlove@naturalsciences.be
Amanda Bendia
administrative point of contact
Universidade de São Paulo
São Paulo
BR
Vivian Pellizari
administrative point of contact
Universidade de São Paulo
São Paulo
BR