Development and application of molecular biomarkers for characterizing Caribbean Yellow Band Disease inOrbicella faveolata

Author:

Morgan Michael1,Goodner Kylia2,Ross James1,Poole Angela Z.3,Stepp Elizabeth4,Stuart Christopher H.5,Wilbanks Cydney1,Weil Ernesto6

Affiliation:

1. Department of Biology, Berry College, Mount Berry, GA, United States

2. Department of Genetics, Yale University, New Haven, CT, United States

3. Department of Biology, Western Oregon University, Monmouth, OR, United States

4. The Medical College of Georgia, Georgia Regents University, Augusta, GA, United States

5. Department of Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States

6. Department of Marine Sciences, University of Puerto Rico, Lajas, Puerto Rico, United States

Abstract

Molecular stress responses associated with coral diseases represent an under-studied area of cnidarian transcriptome investigations. Caribbean Yellow Band Disease (CYBD) is considered a disease ofSymbiodiniumwithin the tissues of the coral hostOrbicella faveolata. There is a paucity of diagnostic tools to assist in the early detection and characterization of coral diseases. The validity of a diagnostic test is determined by its ability to distinguish host organisms that have the disease from those that do not. The ability to detect and identify disease-affected tissue before visible signs of the disease are evident would then be a useful diagnostic tool for monitoring and managing disease outbreaks. Representational Difference Analysis (RDA) was utilized to isolate differentially expressed genes inO. faveolataexhibiting CYBD. Preliminary screening of RDA products identified a small number of genes of interest (GOI) which included an early growth response factor and ubiquitin ligase from the coral host as well as cytochrome oxidase from the algal symbiont. To further characterize the specificity of response, quantitative real-time PCR (qPCR) was utilized to compare the expression profiles of these GOIs within diseased tissues (visible lesions), tissues that precede visible lesions by 2–4 cm (transition area), and tissues from healthy-looking colonies with no signs of disease. Results show there are distinctive differences in the expression profiles of these three GOIs within each tissue examined. Collectively, this small suite of GOIs can provide a molecular “finger print” which is capable of differentiating between infected and uninfected colonies on reefs where CYBD is known to occur.

Funder

Berry College for the Richards Scholarships

NSF-REU

The Berry College Provost’s Office

NSF IOS

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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