Developing Biomarkers for Bloom Growth and Death in Florida Red Tides
Project Status: This project began in January 2013 and was completed in December 2015
The microscopic alga Karenia brevis causes harmful algal blooms (red tides) in the Gulf of Mexico. By studying the processes regulating the life cycle of K. brevis, we developed biomarkers to identify actively growing blooms and signs of blooms in demise. Accurate knowledge of the status of a K. brevis bloom will allow coastal managers to better forecast the impacts of harmful algal blooms.
Why We Care
The occurrence of K. brevis blooms in the northern Gulf of Mexico in the past decade has surpassed previous records, with blooms often persisting in coastal waters for many months. These coastal blooms cause human neurotoxic shellfish poisoning, respiratory irritation when toxin is aerosolized, and extensive fish and marine mammal kills. The impacts on public health, commercial shellfisheries, and tourism cause economic losses in the tens of millions per year. There is currently no simple method to determine the growth phase of a bloom that can be used by managers to better forecast the longevity and impacts of Florida red tides.
What We Are Doing
We are developing fluorescent biomarkers to measure the percentage of cells actively growing in a bloom patch and the percentage showing signs of stress or cell death. For the growth biomarker, we are using expression of the cell cycle protein “PCNA,” which is expressed only in actively dividing cells. To identify cells undergoing cellular stress, we are using a fluorescent tag that identifies cells with high loads of harmful reactive oxygen species inside. To identify cells actively undergoing programmed cell death, we are using an assay called “TUNEL,” which identifies cells suffering from damaged DNA. Using fluorescence detection, these biomarkers can be adapted to flow cytometry, which allows for ship-board application and automated quantification of samples from a bloom patch.
Once our biomarkers are validated in the laboratory, we will test the methods on natural bloom patches in the Gulf of Mexico in collaboration with the Florida Red Tide Monitoring Program. We will then transfer the methodology to regulators responsible for red tide monitoring and management.
Region of Study: Gulf of Mexico
Primary Contact: Fran VanDolah
Harmful Algal Blooms
Related NCCOS Center: CCEHBR
- Johnson, Jillian G. and Frances M. Van Dolah. 2014. Dual localization of Karenia brevis metacaspases (KbMC1) in the chloroplast and cytosol: implication in oxidative stress and cell death. Comparative Biochemistry and Physiology (submitted).
- Johnson, Jillian G., Michael G. Janech, and Frances M. Van Dolah. 2014. Caspase-like activity during aging and cell death in the toxic dinoflagellate Karenia brevis. Harmful Algae 31:41–53.
- Brunelle, Stephanie A. and Frances M. Van Dolah. 2011. Post-transcriptional regulation of S-phase genes in the dinoflagellate, Karenia brevis. Journal of Eukaryotic Microbiology 58(4):373–382.
- Van Dolah, Frances M., Kristy B. Lidie, Emily A. Monroe, Debashish Bhattacharya, Lisa Campbell, Gregory J. Doucette, and Daniel Kamykowski. 2009. The Florida red tide dinoflagellate Karenia brevis: New insights into cellular and molecular processes underlying bloom dynamics. Harmful Algae 8(4):562–572.
- Miller-Morey, Jeanine S. and Frances M. Van Dolah. 2004. Differential responses of stress proteins, antioxidant enzymes, and photosynthetic efficiency to physiological stresses in the Florida red tide dinoflagellate, Karenia brevis. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 138(4):493–505.
* Printed on October 22, 2016 at 7:00 AM from .