Comparison of Niskin vs. in situ approaches for analysis of gene expression in deep Mediterranean Sea water samples

dc.contributor.author Edgcomb, Virginia P.
dc.contributor.author Taylor, Craig D.
dc.contributor.author Pachiadaki, Maria G.
dc.contributor.author Honjo, Susumu
dc.contributor.author Engstrom, Ivory B.
dc.contributor.author Yakimov, Michail M.
dc.date.accessioned 2014-12-03T19:25:03Z
dc.date.available 2014-12-03T19:25:03Z
dc.date.issued 2014-10
dc.description Author Posting. © The Author(s), 2014. This is the author's version of the work. It is posted here by permission of Elsevier for personal use, not for redistribution. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 129 (2016): 213-222, doi:10.1016/j.dsr2.2014.10.020. en_US
dc.description.abstract Obtaining an accurate picture of microbial processes occurring in situ is essential for our understanding of marine biogeochemical cycles of global importance. Water samples are typically collected at depth and returned to the sea surface for processing and downstream experiments. Metatranscriptome analysis is one powerful approach for investigating metabolic activities of microorganisms in their habitat and which can be informative for determining responses of microbiota to disturbances such as the Deepwater Horizon oil spill. For studies of microbial processes occurring in the deep sea, however, sample handling, pressure, and other changes during sample recovery can subject microorganisms to physiological changes that alter the expression profile of labile messenger RNA. Here we report a comparison of gene expression profiles for whole microbial communities in a bathypelagic water column sample collected in the Eastern Mediterranean Sea using Niskin bottle sample collection and a new water column sampler for studies of marine microbial ecology, the Microbial Sampler – In Situ Incubation Device (MS-SID). For some taxa, gene expression profiles from samples collected and preserved 33 in situ were significantly different from potentially more stressful Niskin sampling and 34 preservation on deck. Some categories of transcribed genes also appear to be affected by sample 35 handling more than others. This suggests that for future studies of marine microbial ecology, 36 particularly targeting deep sea samples, an in situ sample collection and preservation approach 37 should be considered. en_US
dc.description.sponsorship This research was funded by NSF OCE-1061774 to VE and CT, NSF DBI-0424599 to CT and NSF OCE-0849578 to VE and colleague J. Bernhard. Cruise participation was partially supported by Deutsche Forschungsgemeinschaft (DFG) grant STO414/10-1 to T. Stoeck. en_US
dc.format.mimetype application/pdf
dc.identifier.uri https://hdl.handle.net/1912/6967
dc.language.iso en_US en_US
dc.relation.uri https://doi.org/10.1016/j.dsr2.2014.10.020
dc.subject Metatranscriptomics en_US
dc.subject Microbial sampler en_US
dc.subject In Situ icubation device en_US
dc.subject Pressure effects en_US
dc.title Comparison of Niskin vs. in situ approaches for analysis of gene expression in deep Mediterranean Sea water samples en_US
dc.type Preprint en_US
dspace.entity.type Publication
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