Marine oxygen minimum zones (OMZs) are widespread regions of the ocean that are currently expanding due to global warming. While inhospitable to most metazoans, OMZs are hotspots for microbial mediated biogeochemical cycling of carbon, nitrogen and sulphur, contributing disproportionately to marine nitrogen loss and climate active trace gas production. Our current understanding of microbial community responses to OMZ expansion is limited by a lack of time-resolved data sets linking multi-omic sequence information (DNA, RNA, protein) to geochemical parameters and process rates. Here, we present six years of time-resolved multi-omic observations in Saanich Inlet, a seasonally anoxic fjord on the coast of Vancouver Island, British Columbia, Canada that undergoes recurring changes in water column oxygenation status. This compendium provides a unique multi-omic framework for studying microbial community responses to ocean deoxygenation along defined geochemical gradients in OMZ waters.
Machine-accessible metadata file describing the reported data (ISA-tab format)
Background & Summary
Marine oxygen minimum zones (OMZs), areas of low dissolved oxygen (O2) in
subsurface waters, result from a combination of microbial respiration of organic
matter raining down from surface waters and increased water column
Advances in sequencing technology are enabling the study of microbial communities at
unprecedented scales16. Tag
sequencing uses primers to amplify specific target genes and subsequently sequence
them on high-throughput platforms, generating molecular barcodes that can be used to
study microbial community structure and function depending on the marker. The small
subunit ribosomal RNA (SSU rRNA) gene is a universally conserved marker commonly
used to compare microbial communities among and between samples in a quantitative
sequencing enables reconstruction of microbial community metabolic potential at the
level of genes and pathways over relatively long time scales reflecting persistent
information storage in the environment. However, metabolic potential does not
necessarily indicate active processes as different genes may be expressed under
changing environmental conditions18. Metatranscriptomic sequencing opens a window into microbial
community gene expression patterns on relatively short time scales reflecting
environmental response patterns18.
Similarly, metaproteomics identifies proteins present in the microbial community on
intermediate times scales, providing an alternative perspective on
post-translational regulation and catalysis18. Collectively, multi-omic methods (DNA, RNA and protein)
can be used to chart microbial metabolism at individual, population and community
levels along defined geochemical gradients in OMZs19,
Saanich Inlet, a seasonally anoxic fjord on the coast of Vancouver Island, British
Columbia is a model ecosystem for studying microbial community responses to changing
levels of water column O2-deficiency8,20,
Here we present a compendium of multi-omic sequence information from the Saanich Inlet water column (Fig. 1) encompassing 412 SSU rRNA pyrotag (V6-V8 region) samples (Data Citation 1: NCBI Sequence Read Archive SRP043213), 82 SSU rRNA iTag (V4 region) samples (Data Citation 1: NCBI Sequence Read Archive SRP043213) (Table 1), 90 metagenomes (Data Citation 1: NCBI Sequence Read Archive SRP043213) (totalling 4.1 TB of cleaned reads or 16.2 GB of assembled data), 62 metatranscriptomes (Data Citation 1: NCBI Sequence Read Archive SRP043213) (including 46 unique samples and 16 replicates, totalling 1.7 TB of cleaned reads or 2.88 GB of assembled data) and 68 metaproteomes (64 unique samples, totalling 5.2 million unique proteins) (Data Citation 2: PRIDE PXD004433) (Table 2). Together sequence read data is approximately 5.9 TB of data, comparable to nearly 2,000 human genome equivalents. These data sets, in combination with a cognate geochemical compendium35 comprise a unique time-resolved framework for reconstructing microbial community metabolism along defined geochemical gradients and promoting the development of models to predict microbial community responses to changing levels of water column oxygen-deficiency11,22,36.
Time-series monitoring in Saanich Inlet was conducted on a monthly basis aboard the MSV John Strickland at station S3 (48°35.500 N, 123°30.300 W) as described in ref. 8. Samples for large volume (LV) SSU rRNA gene tags, metagenomics, metatranscriptomics, and metaproteomics were taken from six major depths spanning the oxycline (10, 100, 120, 135, 150, and 200 m). Samples for high-resolution (HR) SSU rRNA gene tag sequencing were taken at 16 depths along the oxycline (10, 20, 40, 60, 75, 80, 90, 97, 100, 110, 120, 135, 150, 165, 185 and 200 meters). A detailed seawater sampling video protocol can be found online at http://www.jove.com/video/1159/seawater-sampling-and-collection37.
During sampling procedure, large volume waters were collected in 2×12 l Go-Flow bottles on a wire separated by less than one meter. Waters for metatranscriptomics and metaproteomics (2 l each) were collected consecutively from the Go-Flow into 2 l Nalgene bottles with sterile silicon tubing immediately following sampling for dissolved gases to minimise changes in microbial gene expression. Waters for metatranscriptomics were filtered on-board within 8 min of collection on deck, followed immediately by filtering waters for metaproteomics. For both metatranscriptomics and metaproteomics, a peristaltic pump was used to filter waters through a 0.22 μm Sterivex filter with an in-line 2.7 μm GDF pre-filter. Following removal of residual seawater by extrusion using a 10 cc or 60 cc syringe, 1.8 ml of RNAlater (Ambion) was added to metatranscriptomic sample filters and 1.8 ml of sucrose lysis buffer was added to metaproteomic sample filters. Filters were placed on dry ice, returned to lab and stored at −80 °C until processing. A detailed small volume filtration protocol can be found online at http://www.jove.com/video/1163/small-volume-1-3l-filtration-of-coastal-seawater-samples37.
Waters for LV SSU rRNA gene tags and metagenomics were combined from two Go-Flows into a 20 l carboy using sterile silicon tubing. Carboys were then transported back to the lab for filtration approximately 6–10 h after collection. Approximately 10 l was filtered through 2 Sterivex filters per depth as described above. Following removal of residual seawater by extrusion, 1.8 ml of sucrose lysis buffer was added to LV sample filters. Filters were placed on dry ice, returned to lab and stored at −80 °C until processing. A detailed large volume filtration protocol can be found online at http://www.jove.com/video/1161/large-volume-20l-filtration-of-coastal-seawater-samples38.
Waters for high resolution (HR) SSU rRNA gene tags were collected in 12 l Go-Flow or 8 l Niskin bottles and transferred into 1 l (February 2006—September 2009) or 2 l (September 2009 onward) Nalgene bottle with sterile silicon tubing and stored on ice. Bottles were then transported back to the lab for filtration approximately 12–16 h after collection. A peristaltic pump was used to filter waters through a 0.22 μm Sterivex filter without a pre-filter. Following removal of residual seawater by extrusion, 1.8 ml of sucrose lysis buffer was added to HV sample filters. Filters were placed on dry ice, returned to lab and stored at −80 °C until processing. A detailed small volume filtration protocol can be found online at http://www.jove.com/video/1163/small-volume-1-3l-filtration-of-coastal-seawater-samples37.
Environmental DNA, RNA and protein extraction
Genomic DNA (HR and LV) was extracted from Sterivex filters as described in27. Video protocols describing the extraction process in detail can be found online at http://www.jove.com/video/1352/dna-extraction-from-022-m-sterivex-filters-cesium-chloride-density39. Briefly, after thawing Sterivex filters on ice, lysozyme (Sigma) was added and incubated at 37 °C for 1 h with rotation followed by addition of Proteinase K (Sigma) and 20% SDS and incubation at 55 °C for 2 h with rotation. Lysate was removed by extrusion and then filters were rinsed with sucrose lysis buffer. Combined lysate was extracted with phenol:chloroform followed by chloroform and the aqueous layer collected and loaded onto a 10 K Amicon filter (Millipore) cartridge, washed three times with TE buffer (pH 8.0) and concentrated to a final volume between 150–400 μl by centrifugation.
Total RNA was extracted from Sterivex filters using the mirVana miRNA Isolation kit (Ambion)19,25 modified for Sterivex filters. Briefly, after thawing filters on ice, RNAlater was removed by extrusion, followed by rinsing with Ringer’s solution (Sigma) and incubation at room temperature for 20 min with rotation. Ringer’s solution was removed by extrusion, followed by addition of lysozyme and incubation at 37 °C for 30 min with rotation. Lysate was removed by extrusion into 15 ml tube and subjected to organic extraction as described in the mirVana kit protocol, adjusting for total volume of lysate. Removal of DNA and purification of total RNA were conducted using the TURBO DNA-free kit (Thermofisher) and the RNeasy MinElute Cleanup kit (Qiagen) protocols respectively.
Total protein was extracted from Sterivex as described in Hawley et al.40. Briefly, after thawing Sterivex filters on ice, Bugbuster (Novagen) was added and incubated at room temperature for 20–30 min with rotation. Lysate was removed by extrusion and filters were rinsed with 1 ml lysis buffer. Buffer exchange was carried out on combined lysate using Amicon Ultra 10 K (Millipore) with 100 mM NH4HCO3 a total of three times with a final volume between 200–500 μl. Protein concentration was determined using the 2-(4-carboxyquinolin-2-yl) quinoline-4-carboxylic acid (Bicinchoninic acid or BCA) assay. Urea was added to a final concentration of 8 M and dithiothreitol added to a final concentration of 5 mM and incubated at 60 °C for 30 min, followed by 10-fold dilution with 100 mM NH4HCO3. Samples were then subject to trypsin digest at 37 °C for 6 h followed by C18 solid phase extraction and strong cation exchange.
Environmental DNA and RNA sequencing
Extracted genomic DNA was used to generate small subunit ribosomal RNA (SSU or 16S/18S rRNA) gene pyrotag libraries20,41. Pyrotag datasets from HR and LV samples were generated by PCR amplification using universal three-domain forward and reverse bar-coded primers targeting the V6-V8 hypervariable region of the SSU rRNA gene42: 926F (5′- AAA CTY AAA KGA ATT GRC GG-3′) and 1392R (5′- ACG GGC GGT GTG TRC-3′). Samples were purified using the QIAquick PCR Purification Kit (Qiagen), and sequenced by 454-pyrosequencing43 at the DOE Joint Genome Institute (JGI), or Génome Québec Innovation Centre at McGill University (Table 3 and Supplementary Table 1). iTag datasets from HR and LV samples were generated by PCR amplification using forward and reverse bar-coded primers targeting the V4-V5 hypervariable region of the bacterial and archaeal SSU rRNA gene: 515F (5′- Y GTG YCA GCM GCC GCG GTAA—3′) and 806R (5′- CCG YCA ATT YMT TTR AGT TT -3′)44,45. Samples were sequenced according to the standard operating protocol on an Illumina MiSeq platform at the JGI46.
Ilumina metagenomic shotgun libraries from LV samples were generated at the JGI
and paired end sequenced on the Illumina HiSeq platform43,47,
Environmental protein sequencing
Extracted environmental protein was sequenced using tandem mass spectrometry (MS/MS) as described previously40. Samples were analysed by capillary liquid chromatography-tandem mass spectrometry (Thermo, LTQ ion trap mass spectrometer or Thermo LTQ-Orbitrap mass spectrometer) in data-dependent mode. Spectra were matched to peptide sequences using the search tool MSGFDBPlus54. The amino acid sequence database used for matching spectra to protein sequences was constructed from metagenomic information from Saanich Inlet and the Line P transect in the Northeastern subarctic Pacific Ocean with additional full-length fosmid libraries20, and single cell genomes from Saanich Inlet55 totalling over 23 million protein sequences.
Small subunit rRNA gene tag sequences
Small subunit rRNA gene pyrotag and iTag sequences are available from the National Center for Biotechnology Information (NCBI) Sequence Read Archive (Data Citation 1: NCBI Sequence Read Archive SRP043213). A summary of Pyrotag and iTag samples can be located in Table 1, key to the Pyrotag and iTag data files is located in Table 3 and NCBI BioSample IDs and sequencing centre information for individual samples are located in Supplementary Table 1. In addition, previously published full length small subunit rRNA gene libraries27 are archived at GenBank.
Metagenomes and Metatranscriptomes
Metagenomic and metatranscriptomic data sets are accessible through the JGI IMG/M portal (https://img.jgi.doe.gov/cgi-bin/m/main.cgi) under the study name Marine microbial communities from expanding oxygen minimum zones in the northeastern subarctic Pacific Ocean (Data Citation 1: NCBI Sequence Read Archive SRP043213). A unifying inventory of metagenomes, metatranscriptomes and metaproteomes sequenced for the Saanich Inlet time-series is summarised in Table 2, with key in Supplementary Table 2 (Data Citation 1: NCBI Sequence Read Archive SRP043213). Sanger sequenced fosmid library28, 454 and Illumina sequenced metagenomic libraries20,21 and 454 sequenced viral metagenomes33 have been previously published.
Metaproteomic datasets have been deposited in the ProteomeXchange Consortium via the PRIDE56 partner repository with the dataset identifier PXD004433 (Data Citation 2: PRIDE PXD004433). The key detailing the file types available on the PRIDE repository is located in Table 5. Previously published metaproteomic data sets20 were archived at Mass Spectrometry Interactive Virtual Environment.
Small subunit ribosomal RNA gene tag sequences
For SSU rRNA gene pyrotags and iTags the quality of extracted genomic DNA was verified on 0.8% agarose gels stained with ethidium bromide or SYBR Safe DNA dye (Thermofisher). Samples were run at 16 V overnight with molecular ladders (10 μl of 50 ngml−1 of 1 kb+; 2, 5 and 10 μl of 50 ngml−1 HindIII ladder) to determine size and estimate concentration of extracted sample DNA (5 μl of extract run on gel). After running, the gel was observed under a UV gel documentation system to check for approximate molecular weight (>36 kb) and evidence of shearing or degradation. In addition, DNA concentration was quantified and corrected to volume filtered using PicoGreen (Thermofisher) following the vendor’s protocol.
Quality control for 454-pyrosequencing entails accurate quantification of prepared library fragments to optimize the sequencing run output, therefore JGI has developed custom qPCR methods to quantify 454 libraries43. In addition, an optimized emulsion PCR protocol was developed to significantly improve the coverage in high GC regions that otherwise would be biased49. Génome Québec Innovation Centre quality control protocol for 454 pyrosequencing entails the use of the default parameters assigned to the signal processing software for Long Amplicon #3 pipeline as indicated in the Roche ‘454 Sequencing System Software Manual’ V3.0 Section 1.353. For produced 454 pyrotag datasets for both high resolution (HR) and large volume (LV) samples a histogram of raw read counts versus read length (Fig. 2a) was used to determine the success of a run e.g. a majority of reads exceeding 450 base pairs. A plot of read counts versus read length for all HR and LV samples is provided in Fig. 2a.
Quality control protocol for iTag sequencing entails QC amplification with V4-V5 primers prior to sample submission to ensure that samples will be successful in JGI sample prep and that there are no contaminants present that will inhibit amplification. Amplified products are run on agarose gel or Bioanalyzer to ensure sample amplification occurred with the expected band size, ~450 bp for bacterial and archaeal SSU rRNA gene V4-V5 region (including primers). Samples showing proper amplification and sizing are passed for Amplification QC and approved to ship to the JGI for processing. All data from the sequencer were demultiplexed and stored in JGI’s archiving and metadata organizer system (JAMO). Read data was processed through JGI’s centralized rolling quality control system verifying that there were no sequencing issues and removing known contaminant reads using a kmer filter in bbduk. Quality controlled reads were processed by iTagger45,46.
Metagenomic and metatranscriptomic data validation
The quality of DNA used for metagenomic sequencing was determined at the same time as verification for SSU rRNA gene pyrotag and iTag amplification as described above. JGI quality control protocol for metagenomic sequences prior to assembly entails rolling QC, an in-house sequence QC pipeline that performs a set collection of analyses and produces a summary report for each lane of Illumina data produced by the sequencing group. This set of analyses calculates read quality, measures sequence uniqueness, and detects abnormal sequence motifs. An assembly, using Velvet, was used to measure coverage and detect contamination48. For individual sample assemblies the average fold coverage versus the contig length (Fig. 2b) was plotted and should have a distinct shape for different samples where peaks in contig length representing at a specific coverage represent a given closely related microbial population. Additionally, the percent GC versus average coverage can be plotted, again with distinct shapes for different samples and clusters representing divergent microbial populations.
The quality of purified RNA was verified on the Bioanalyzer using a RNA nano Analysis Kit (Agilent Technologies) in order to check on the RNA integrity and sample quantification before cDNA library production and sequencing at JGI. Due to variation inherent in environmental samples the RNA integrity number (RIN) varied between 5.5 and 9 for the sample sand averaged 7.3. JGI quality control protocol for metatranscriptomic sequencing preparation follows the ‘TruSeq Stranded Total RNA Sample Preparation Guide’ (Illumina). Briefly this protocol removed ribosomal rRNA with RiboZero, followed by RNA fragmentation for first strand cDNA synthesis. This was followed by second strand synthesis and subsequent ligation of adapters. After PCR amplification library quality was checked using Bioanalyzer for fragment size (260 bp) and purity. Indexed (barcoded) libraries were normalized to 10 nM and pooled in equal volumes. Transcriptomes were assembled de novo and or mapped to a corresponding metagenome. For Additional quality assessment of sequencing run for each sample, histograms of percentage of reads verse average read quality and of reads per percent GC were generated (Fig. 3a). Information on run quality for individual samples is available via the JGI genome portal.
Metaproteomic data validation
The quality of LC-MS runs were monitored visually by the instrument operator by individually inspecting each analytical run for instrument response, retention time characteristics, and background interference. QC was further monitored using a whole cell digest of Shewanella oneidensis that is prepared in bulk and routinely used across all LC-MS systems in the EMSL production labs. Analysis of this QC standard is fully automated once uploaded to an in-house data management system and reports back unique peptide identifications, chromatographic peak width, and mass error within ~1 h. Additionally, these data are subjected to dozens of other analytical metrics that can be further assessed as needed (i.e., when the first pass visual and 1 h results are in question). This QC standard was run at least once per week but generally more often, between sample batches (a single project), and sometimes between sample blocks (when a batch is relatively large and a blocking scheme has been utilized) due to the large diversity of samples analysed in-house. New LC columns were conditioned and tested prior to use on project samples by running a minimum of three QC standards. Blanks were always run between QC standards and between sample batches, but not necessarily between sample blocks. For peptide mapping to full length protein sequences the False Discovery Rate (FDR) was calculated using the spectra to peptide matches that resulted in reversed hits from the on-the-fly reversed database search and a filter on the MSGF value. Number of peptides and proteins detected varies between samples (Fig. 3b). Due to the large size of metagenomic dataset used and redundancy in protein sequences because of multiple sampling of the same environment in the Saanich Inlet time series most peptides mapped to multiple identical proteins, resulting in a greater number of proteins identified then peptides.
Suggested modes of downstream data analysis
In brief we describe the main workflow used in the analysis of SSU rRNA gene pyrotag and iTag datasets. Tag sequences were clustered into operational taxonomic units (OTUs) using the Quantitative Insights Into Microbial Ecology (QIIME) software package57 and annotated using the SILVA or GreenGenes databases58,59. Community structure was determined using relative abundance and distribution of obtained microbial OTUs along with statistical analyses such as hierarchical clustering and indicator species analysis to identify characteristic groups of OTUs occurring under specific water column conditions such as different water column O2 concentrations.
Illumina metagenomes, metatranscriptomes and metaproteomes were analysed using MetaPathways (version 2.0 and 2.5), an open source pipeline for functional annotation and prediction of reactions and pathways in metagenomes and metatranscriptomes60. Direct link to software download and specifications can be found online on the Hallam Lab Github repository (https://github.com/hallamlab/metapathways2).
With respect to the metaproteomic datasets there is redundancy in the protein database used for peptide mapping in that amino acid sequences will have different names but identical sequences, and thus a given peptide may map to multiple sequences. To manage this one could cluster the proteins by sequence identity at the amino acid level prior to mapping. In previous publications we have calculated a normalised spectral abundance factor (NSAF) as a pseudo-quantative metric to compare abundance of the same proteins between samples40.
How to cite this article: Hawley, A. K. et al. A compendium of multi-omic sequence information from the Saanich Inlet water column. Sci. Data 4:170160 doi: 10.1038/sdata.2017.160 (2017).
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Hallam, S., & Monroe, M. PRIDE PXD004433 (2017)
We thank Captain Ken Brown and his crew for their engaged effort on every cruise aboard the RSV Strickland. We also thank past and present members of the Hallam lab and the many undergraduate trainees, aka minions, for contributions to cruise preparation and clean up, water filtration, DNA extraction and QC. We also thank Tortell lab members for logistical support. This work was performed under the auspices of the US Department of Energy (DOE) Joint Genome Institute an Office of Science User Facility, supported by the Office of Science of the U.S. Department of Energy under Contract DE-AC02- 05CH11231, the G. Unger Vetlesen and Ambrose Monell Foundations, the Tula Foundation-funded Centre for Microbial Diversity and Evolution, the Natural Sciences and Engineering Research Council of Canada, Genome British Columbia, the Canada Foundation for Innovation, and the Canadian Institute for Advanced Research through grants awarded to S.J.H. Ship time support was provided by NSERC between 2007-2014 through grants awarded to S.J.H. and P.D.T. Metaproteomics support came from the intramural research and development program of the W.R. Wiley Environmental Molecular Sciences Laboratory (EMSL). EMSL is a national scientific user facility sponsored by the US DOE’s Office of Biological and Environmental Research and located at the Pacific Northwest National Laboratory operated by Battelle for the US DOE. M.T-B. was funded by Consejo Nacional de Ciencia y Tecnología (CONACyT) and the Tula Foundation. A.K.H. was supported by the Tula Foundation.