| Contributors | Affiliation | Role |
|---|---|---|
| Apprill, Amy | Woods Hole Oceanographic Institution (WHOI) | Co-Principal Investigator |
| Brandt, Marilyn | University of the Virgin Islands Center for Marine and Environmental Studies (UVI) | Co-Principal Investigator |
| Becker, Cynthia Carroll | Woods Hole Oceanographic Institution (WHOI) | Student |
| Bloomberg, Jeanne | Woods Hole Oceanographic Institution (WHOI) | Student |
| Meiling, Sonora | University of the Virgin Islands Center for Marine and Environmental Studies (UVI) | Technician |
| Rauch, Shannon | Woods Hole Oceanographic Institution (WHOI BCO-DMO) | BCO-DMO Data Manager |
Samples were collected on day-trips aboard a University of the Virgin Islands powerboat in the U.S. Virgin Islands from July 2020 through March 2024. On SCUBA, 60 milliliters (mL) of seawater was collected 2-5 centimeters (cm) above the colony surface, then the coral fragment was collected; upon surfacing, samples were put on ice. Seawater was passed through 0.2-micrometer (µm) filters, and the tissue was removed from the skeleton using PBS solution and an airbrush. DNA was extracted from the coral tissue, seawater filters, and processing controls using the Qiagen DNeasy PowerBiofilm Kit. PCR was used to amplify the V4 region of the small subunit rRNA gene of bacteria and archaea using primers 515FY and 806RB with standard barcodes. To purify the PCR product from seawater, the Qiagen PCR Purification Kit was used. Purification of PCR products from coral tissue proceeded by running products in a 1.5% agarose gel and excising bands of 450 bp. Gel excisions were purified using the Qiagen Gel Extraction Kit. PCR products were diluted to 1 nanogram per microliter (ng/μL) and sequenced on an Illumina MiSeq (paired reads, 2x250 nt) at the University of Georgia's Georgia Genomics and Bioinformatics Core and University of Illinois Urbana-Champaign's Roy J. Carver Biotechnology Center.
- Imported original file "sra_result.csv" into the BCO-DMO system.
- Renamed fields to comply with BCO-DMO naming conventions.
- Saved the final file as "986592_v1_ncbi_sra.csv".
| File |
|---|
986592_v1_ncbi_sra.csv (Comma Separated Values (.csv), 36.40 KB) MD5:01b778f9b8d15875af642be2015d8644 Primary data file for dataset ID 986592, version 1 |
| Parameter | Description | Units |
| Experiment_Accession | NCBI experiment accession number | unitless |
| Instrument | Sequencing instrument used | unitless |
| Study_Accession | NCBI study accession number | unitless |
| Study_Title | Title of study on NCBI | unitless |
| Sample_Accession | NCBI sample accession number | unitless |
| Library_Name | Sample name used during the experiment | unitless |
| Collection_date | Date that the sample was collected from reef site | unitless |
| Latitude | Latitude of reef site | decimal degrees |
| Longitude | Latitude of reef site | decimal degrees |
| Dataset-specific Instrument Name | agarose gel |
| Generic Instrument Name | Agarose Gel Electrophoresis System |
| Dataset-specific Description | Purification of PCR products from coral tissue proceeded by running products in a 1.5% agarose gel and excising bands of 450 bp. |
| Generic Instrument Description | A gel electrophoresis system that is used to separate DNA or RNA molecules by size, achieved by moving negatively charged nucleic acid molecules through an agarose matrix with an electric field. |
| Dataset-specific Instrument Name | Illumina MiSeq V2 |
| Generic Instrument Name | Automated DNA Sequencer |
| Dataset-specific Description | Samples were sequenced on an Illumina MiSeq V2. |
| Generic Instrument Description | A DNA sequencer is an instrument that determines the order of deoxynucleotides in deoxyribonucleic acid sequences. |
| Dataset-specific Instrument Name | SCUBA |
| Generic Instrument Name | Self-Contained Underwater Breathing Apparatus |
| Dataset-specific Description | Samples were collected by SCUBA divers. |
| Generic Instrument Description | The self-contained underwater breathing apparatus or scuba diving system is the result of technological developments and innovations that began almost 300 years ago. Scuba diving is the most extensively used system for breathing underwater by recreational divers throughout the world and in various forms is also widely used to perform underwater work for military, scientific, and commercial purposes.
Reference: https://oceanexplorer.noaa.gov/technology/technical/technical.html |
| Dataset-specific Instrument Name | PCR |
| Generic Instrument Name | Thermal Cycler |
| Dataset-specific Description | PCR was used to amplify the V4 region of the small subunit rRNA gene of bacteria and archaea using primers 515FY and 806RB with standard barcodes. |
| Generic Instrument Description | A thermal cycler or "thermocycler" is a general term for a type of laboratory apparatus, commonly used for performing polymerase chain reaction (PCR), that is capable of repeatedly altering and maintaining specific temperatures for defined periods of time. The device has a thermal block with holes where tubes with the PCR reaction mixtures can be inserted. The cycler then raises and lowers the temperature of the block in discrete, pre-programmed steps. They can also be used to facilitate other temperature-sensitive reactions, including restriction enzyme digestion or rapid diagnostics.
(adapted from http://serc.carleton.edu/microbelife/research_methods/genomics/pcr.html) |
NSF Award Abstract:
Marine diseases have devastating impacts on ocean ecosystems and this work will directly examine the framework for understanding disease transmission in the ocean. A team of ecologists, ocean connectivity and disease modelers, microbiologists, and coral immunologists (from the University of Virgin Islands (UVI), Louisiana State University (LSU), Rice University, University of Texas-Arlington and the Woods Hole Oceanographic Institution) will develop a model that predicts transmission of a devastating Caribbean coral disease that has the potential to impact the economic value of coral reefs, including those located in the U.S. This project will support multidisciplinary field and laboratory research experiences of graduate students at multiple minority-serving institutions, and will provide undergraduate students with hands-on training in modeling, ecological and molecular analysis techniques. UVI and LSU are in EPSCoR jurisdictions and have diverse student bodies, including numerous under-represented minority (URM) students. The research team will collaboratively provide URM students with research experiences in STEM fields. Project findings will be broadly communicated through virtual public programming, and through the Virgin Islands Coral Disease Advisory Committee with updates on the vicoraldisease.org website. A coral disease response workshop for the U.S. Virgin Islands will also be held, in which project results will be presented and used to support disease response planning.
Over the last four decades, marine diseases have decimated ecosystem engineers in marine coastal ecosystems, including the rocky intertidal, seagrasses and coral reefs. The pathogens driving these diseases have frequently been challenging to isolate, characterize and confirm, in part because they affect multiple host species and can spread by ocean currents, as well as through individual contact. Here, we propose a multi-scale epidemic model for studying marine disease that addresses both within-host and within-patch disease dynamics, and explicitly acknowledges the dispersal of pathogens between populations. Our interdisciplinary research team of ecologists, connectivity and disease modelers, microbiologists, and coral immunologists will integrate the largest set of predictors of marine disease spread to date: individual host species traits that allow for disease resistance or susceptibility, local transmission within communities that may have unique community structure, and hydrodynamic connectivity among susceptible communities. Modeling will be supported with rich data sets of within- and among-patch population characteristics and disease dynamics as well as molecular data on species-level disease responses. This project will advance knowledge of infectious diseases by integrating multidimensional scales and differential host susceptibilities into existing epidemiological models. This model will particularly advance the framework for studying marine diseases and has the potential to elucidate the transmission properties of a devastating Caribbean coral disease (stony coral tissue loss disease) that fits the most confounding and notorious hallmarks of marine diseases: infection of multiple hosts by an elusive pathogen.
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
| Funding Source | Award |
|---|---|
| NSF Division of Ocean Sciences (NSF OCE) |