Reef corals in the Mexican Reef System have been severely affected by the emergence of a white syndrome that resembles both White Plague II and SCTLD descriptions. Meandroid scleractinian coral species are among the most severely affected. To gain insight into this affliction we conducted a broad study in the brain coral Pseudodiploria strigosa at a rear reef site in the NE Mexican Caribbean. We describe macro and microscopical signals of the disease, characterize the outbreak dynamics, the tissue histopathology, explore immunological responses in the individuals, and compare microbial assemblages associated with the surface mucus layer of healthy and unhealthy colonies. At the study site, the white syndrome outbreak on P. strigosa showed a high incidence rate in summer-fall and a low one in winter, as well as low survival expectation of diseased colonies at the end of the study. After 306 days of observation, out of 96 tracked colonies, eight remained apparently healthy and seven were diseased. No effective resistance to colony disease progression was observed once white syndrome signs developed. Tissue loss rate during the study varied among colonies (mean = 10.8 cm2, s.d. = 7.8 cm2) suggesting a complex relation between causal agents and colony resistance. The deterioration of tissues was evidenced from the basal to the surface body wall of polyps (up to 66% hypertrophy and liquefactive necrosis in unhealthy colonies), implying that microscopic alterations begin before macroscopic signals develop, suggesting this may be a systemic disease. We measured high levels of phenoloxidase (two orders of magnitude higher PO activity than P. strigosa affected by BBD) and antibacterial activity without significant reduction in unhealthy samples from the mucus layer, indicative of an enhanced immunological response. Results showed that opportunistic bacteria dominated damaged colonies, where six genera of the Bacteroidia class were found with significant changes in unhealthy colonies after DeSeq2 analysis. Nevertheless, histological observations did not support infection of the tissues. The opportunistic overload seems to be contained within the mucus layer but may be associated with the mortality of tissues in a yet unclear way. Future research should focus on experimental infections, the tracking of natural infections, and the immunocompetence of corals in the face of environmental pressures due to local, regional, and global impacts. If environmental deterioration is the primary cause of the continuing emergence and re-emergence of lethal coral diseases, as has been proposed by many authors, the only true option to effectively help preserve the coral reef biodiversity and services, is to restore the environmental quality of reef waters at the local scale and reduce greenhouse gases at the global scale.
Rivera-Ortega and Thomé Antibacterial Capabilities of SML in Symbiotic Cnidarians In this work, we show that the surface mucus layer itself has antibacterial properties not associated with the bacteria this layer houses; such properties diminished due to disease or bleaching, while immunological responses increased in the mucus of diseased animals.
Corals are an association between animals and plants that deposit a skeleton and build reefs. Coral reefs are now in danger because the marine environment around them is degrading, causing corals to get ill more often. Scientists have used fragments of healthy coral colonies or planted baby corals to help restore reefs that are in bad shape. But for these e orts to succeed, it is vital for the scientists to select healthy corals for planting. Corals use a substance called melanin to trap bacteria that grows in their tissues. We discovered that the enzyme phenoloxidase, which is responsible for making melanin, can be found in the snotty covering of corals, called mucus. We can take samples of this mucus to measure phenoloxidase without harming the corals. By doing so, we can detect whether a coral colony is responding to the presence of harmful bacteria even before it shows any signs of illness.
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