Dataset: 16S microbiome metadata collected from shallow artificial reef sponges and seawater in the Florida Keys, USA from Apr 2021 to Aug 2021

ValidatedFinal with updates expectedDOI: 10.26008/1912/bco-dmo.953999.1Version 1 (2025-02-21)Dataset Type:Other Field Results

Principal Investigator: Cole G. Easson (Middle Tennessee State University)

Co-Principal Investigator: Cara L. Fiore (Appalachian State University)

Co-Principal Investigator: Christopher J. Freeman (College of Charleston)

Co-Principal Investigator: Robert W. Thacker (Stony Brook University)

BCO-DMO Data Manager: Audrey Mickle (Woods Hole Oceanographic Institution)


Project: Collaborative Research: Investigations into microbially mediated ecological diversification in sponges (Ecological Diversification in Sponges)


Abstract

Sponges are a dominant component of coral reefs worldwide and in the Caribbean, where their biomass exceeds that of reef-building corals. For almost a quarter century, the success of sponges in the Caribbean has been linked to their filter-feeding ability. However, recent work demonstrated that coexisting sponges on Caribbean reefs host unique communities of bacteria that might allow sponges to access multiple pools of nutrients that are not available to other organisms. In this project, the inv...

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Location
Samples were collected on shallow reefs (<10m) in the Florida Keys, USA. The temporary artificial reef was constructed adjacent to patch reefs within the Looe Key special preservation area. At the conclusion of the experiment, the reef was completely dismantled. The environment was well mixed by wave action within minimal tidal influence.

Collection and Analysis

Seawater samples were collected via VacuSIP and filtered through 0.2 µm membranes with a peristaltic pump to collect samples of ambient microbes. Total genomic DNA was extracted from cross sections of sponge tissue (~0.25 grams) and ½ of seawater filter membranes using Qiagen PowerSoil Powerlyzer extraction kit and following the manufacturers protocol. After DNA extraction, polymerase chain reaction (PCR) was performed following the 16S Illumina Amplicon protocol of the Earth Microbiome project (Caporaso, 2018) with barcoded 16S rRNA primers (515F and 806R; (Apprill et al. 2015, Parada et al. 2016) and PCR products were cleaned using AMPure beads (Beckman Coulter). DNA concentration in cleaned products was measured using a Qubit fluorometer (Qubit). The concentration of each sample was diluted to 4 nM and then all samples were pooled in equal volumes. Pooled samples were then sequenced on an Illumina MiSeq platform following standard Illumina protocols for sample preparation and loading except that custom sequencing primers from the EMP protocol were used. A 500 cycle V2 chemistry MiSeq kit was used during sequencing, which yielded paired-end 250 base pair (bp) amplicons.


Related Datasets

Related Research

Dataset: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1179970
Middle Tennessee State University (2024). InEx and Sponge microbiome samples. 2024/10. NCBI:BioProject: PRJNA1179970. Bethesda, MD: National Library of Medicine (US), National Center for Biotechnology Information. Available from: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1179970.

Related Publications

Methods

Apprill, A., McNally, S., Parsons, R., & Weber, L. (2015). Minor revision to V4 region SSU rRNA 806R gene primer greatly increases detection of SAR11 bacterioplankton. Aquatic Microbial Ecology, 75(2), 129–137. doi:10.3354/ame01753
Methods

Greg Caporaso, J., Ackermann, G., Apprill, A., Bauer, M., Berg-Lyons, D., Betley, J., Fierer, N., Fraser, L., A. Fuhrman, J., A. Gilbert, J., Gormley, N., Humphrey, G., Huntley, J., K. Jansson, J., Knight, R., L. Lauber, C., A. Lozupone, C., McNally, S., M. Needham, D., … Weber, L. (2018). EMP 16S Illumina Amplicon Protocol v1. https://doi.org/10.17504/protocols.io.nuudeww
Methods

Morganti, T., Yahel, G., Ribes, M., & Coma, R. (2016). VacuSIP, an Improved InEx Method for &lt;em&gt;In Situ&lt;/em&gt; Measurement of Particulate and Dissolved Compounds Processed by Active Suspension Feeders. Journal of Visualized Experiments, 114. https://doi.org/10.3791/54221
Methods

Parada, A. E., Needham, D. M., & Fuhrman, J. A. (2016). Every base matters: assessing small subunit rRNA primers for marine microbiomes with mock communities, time series and global field samples. Environmental Microbiology, 18(5), 1403–1414. doi:10.1111/1462-2920.13023