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  DNA/RNA Preservation in Glacial Snow and Ice Samples

Trivedi, C. B., Keuschnig, C., Larose, C., Rissi, D., Mourot, R., Bradley, J., Winkel, M., Benning, L. G. (2022): DNA/RNA Preservation in Glacial Snow and Ice Samples. - Frontiers in Microbiology, 13, 894893.
https://doi.org/10.3389/fmicb.2022.894893

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 Creators:
Trivedi, Christopher B.1, Author              
Keuschnig, Christoph2, Author              
Larose, Catherine3, Author
Rissi, Daniel1, Author              
Mourot, Rey1, Author              
Bradley, James1, Author              
Winkel, Matthias1, Author              
Benning, Liane G.1, Author              
Affiliations:
13.5 Interface Geochemistry, 3.0 Geochemistry, Departments, GFZ Publication Database, Deutsches GeoForschungsZentrum, ou_754888              
20 Pre-GFZ, Departments, GFZ Publication Database, Deutsches GeoForschungsZentrum, ou_146023              
3External Organizations, ou_persistent22              

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 Abstract: The preservation of nucleic acids for high-throughput sequencing is an ongoing challenge for field scientists. In particular, samples that are low biomass, or that have to be collected and preserved in logistically challenging environments (such as remote sites or during long sampling campaigns) can pose exceptional difficulties. With this work, we compare and assess the effectiveness of three preservation methods for DNA and RNA extracted from microbial communities of glacial snow and ice samples. Snow and ice samples were melted and filtered upon collection in Iceland, and filters were preserved using: (i) liquid nitrogen flash freezing, (ii) storage in RNAlater, or (iii) storage in Zymo DNA/RNA Shield. Comparative statistics covering nucleic acid recovery, sequencing library preparation, genome assembly, and taxonomic diversity were used to determine best practices for the preservation of DNA and RNA samples from these environments. Our results reveal that microbial community composition based on DNA was comparable at the class level across preservation types. Based on extracted RNA, the taxonomic composition of the active community was primarily driven by the filtered sample volume (i.e., biomass content). In low biomass samples (where <200 ml of sample volume was filtered) the taxonomic and functional signatures trend toward the composition of the control samples, while in samples where a larger volume (more biomass) was filtered our data showed comparable results independent of preservation type. Based on all comparisons our data suggests that flash freezing of filters containing low biomass is the preferred method for preserving DNA and RNA (notwithstanding the difficulties of accessing liquid nitrogen in remote glacial field sites). Generally, RNAlater and Zymo DNA/RNA Shield solutions work comparably well, especially for DNA from high biomass samples, but Zymo DNA/RNA Shield is favored due to its higher yield of preserved RNA. Biomass quantity from snow and ice samples appears to be the most important factor in regards to the collection and preservation of samples from glacial environments.

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 Dates: 2022-05-232022
 Publication Status: Finally published
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 Identifiers: DOI: 10.3389/fmicb.2022.894893
GFZPOF: p4 T5 Future Landscapes
GFZPOFCCA: p4 CTA Extrems
OATYPE: Gold Open Access
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Project name : "Gefördert im Rahmen des Förderprogramms "Open Access Publikationskosten" durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491075472".
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Funding program : Open-Access-Publikationskosten (491075472)
Funding organization : Deutsche Forschungsgemeinschaft (DFG)

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Title: Frontiers in Microbiology
Source Genre: Journal, SCI, Scopus, oa
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Pages: - Volume / Issue: 13 Sequence Number: 894893 Start / End Page: - Identifier: CoNE: https://gfzpublic.gfz-potsdam.de/cone/journals/resource/131115
Publisher: Frontiers