virome_antarctic_lakes_2010
Citation
de Carcer D A, Lopez-Bueno A, Alonso-Lobo J, Quesada A, Alcami A, Sweetlove M (2021). virome_antarctic_lakes_2010. SCAR - Microbial Antarctic Resource System. Metadata dataset https://doi.org/10.15468/gcysrw accessed via GBIF.org on 2024-12-11.Description
Virome dataset based on shotgun 454 sequencing of virus-concentrated samples from lakes in the Antarctic Peninsula (2010).Sampling Description
Study Extent
Samples were taken from several freshwater bodies in the Antarctic Peninsula during the Austral summer 2010.Sampling
Water samples were preserved at 4°C and viral particles purified within the first 24 h of sampling. From each water body, 60–90 l were first filtered through a 30 μm nylon mesh to remove large particles, and then by tangential flow filtration (TFF) using a peristaltic pump coupled to a Centramate holder (Pall) with two cassettes of 0.45 μm (2 × 0.019 m2, PES) to remove bacteria and smaller eukaryotes.Method steps
- The filtrated viral fraction was concentrated 100 times by TFF with two cassettes of 70 kDa exclusion size at pressures below 10 p.s.i., in order to maintain viral particle integrity. Viral stocks were preserved at −20°C for transportation, and finally stored at −80°C before subsequent processing. All material was acid-rinsed (0.1 N HCl) and extensively washed with Milli Q or 70 kDa-filtered lake water.
- Frozen stocks were thawed at 4°C with gentle rocking, and then passed through a 25% sucrose cushion by centrifugation for 16 h at 60 000 g and 4°C. The resulting pellets were resuspended in TE buffer (10 mM Tris pH 8, 1 mM EDTA), and filtered using a sterile 0.45 μm syringe filter. Viral concentrates were then treated with DNAse I (500 U ml−1), Nuclease S7 (500 U ml−1), RNAse A (100 μg ml−1) and RNAse H (2 U per reaction) for 30 min at room temperature to remove free nucleic acids. Nuclease reactions were stopped with EDTA and EGTA (12 and 2 mM, respectively), and viral capsids and envelopes were then disrupted with SDS (0.5%) and proteinase K (200 μg ml−1) treatment.
- Viral DNA was extracted with phenol–chloroform, ethanol precipitated and randomly amplified using Phi29 polymerase and modified random hexamers (GenomiPhi HY, GE Healthcare) for 2.5 h, according to the manufacturer's instructions. The samples were subsequently shot-gun sequenced with a Roche 454 FLX sequencer (Parque Científico de Madrid).
Taxonomic Coverages
Geographic Coverages
Antarctic Peninsula: Caleta Cierva, Avian Island, Green Island, Pourquoi Pas Island and Livingston Island (South Shetland Islands)
Bibliographic Citations
- de Cárcer A. D., López-Bueno A., Alonso-Lobo J. M., Quesada A., & Alcamí A. (2016). Metagenomic analysis of lacustrine viral diversity along a latitudinal transect of the Antarctic Peninsula. FEMS microbiology ecology, 92(6), fiw074. -
Contacts
Daniel Aguire de Carceroriginator
Universidad Autónoma de Madrid
Madrid
ES
Alberto Lopez-Bueno
originator
Universidad Autónoma de Madrid
Madrid
ES
Juan Alonso-Lobo
originator
Universidad Autónoma de Madrid
Madrid
ES
Antonio Quesada
originator
Universidad Autónoma de Madrid
Madrid
ES
Antonio Alcami
originator
Universidad Autónoma de Madrid
Madrid
ES
Maxime Sweetlove
metadata author
Royal Belgian Institute of Natural Sciences
Brussels
BE
email: msweetlove@naturalsciences.be
Antonio Alcami
user
Universidad Autónoma de Madrid
Madrid
ES
Antonio Alcami
administrative point of contact
Universidad Autónoma de Madrid
Madrid
ES