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Occurrence of ultraviolet radiation-absorbing mycosporine-like amino acids in coral mucus and whole corals of French Polynesia

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Specimens of six scleractinian species were gathered during the austral spring (October–November) 1994 on the external slope of the barrier reef of Arue, Tahiti, and in the lagoon of Arutua, a Tuamotu island. Mucus of each specimen was collected and the optical density and volume excreted were measured. After treatment, mucus was analysed for mycosporine-like amino acids (MAAs) by high-performance liquid chromatography (HPLC). Nine UV-absorbing compounds were present in coral mucus at concentrations between 1 and 500 ng g-1 mucus. Palythine and mycosporine–gly were found in all mucus studied. Mycosporine–2glycine was recovered in 71% of specimens and shinorine in 28%. Porphyra-334 and palythinol were identified as minor MAAs. Three recently identified MAAs, palythine–serine, mycosporine–methylamine:serine and mycosporine–methylamine:threonine, were also found in mucus from Pocillopora. Within a genus, there was a qualitative similarity in MAAs determined by HPLC, irrespective of locality. Values for optical density of the mucus showed the ability of MAAs to protect the animal host and endosymbiotic algae from UV-solar flux and, as inferred from the recent literature, from oxidative forms of oxygen (HO2 . , O 2- , HO.) derived from photosynthesis.
... This mechanism is critical for the survival of corals, as exposure to high levels of UV radiation can cause damage to coral DNA, resulting in a range of negative impacts on coral health and the overall health of the surrounding ecosystem. By providing this important protection against UV radiation, MAAs play a key role in maintaining the health and resilience of coral populations (Teai et al. 1998;Kageyama and Waditee-Sirisattha 2019). Mycosporine-glycine, mycosporine-2glycine, palythine, mycosporine-methylamine-serine, and mycosporine-methylamine-threonine, which were characterized from Lobophyllia, Acropora, Fungia, and Pocillopora species, have all been reported from coral mucus (Teai et al. 1998). ...
... By providing this important protection against UV radiation, MAAs play a key role in maintaining the health and resilience of coral populations (Teai et al. 1998;Kageyama and Waditee-Sirisattha 2019). Mycosporine-glycine, mycosporine-2glycine, palythine, mycosporine-methylamine-serine, and mycosporine-methylamine-threonine, which were characterized from Lobophyllia, Acropora, Fungia, and Pocillopora species, have all been reported from coral mucus (Teai et al. 1998). In addition to their ability to combat oxidative stress, MAAs can protect many marine organisms from the harmful effects of light (Shick and Dunlap 2002). ...
... In addition to their ability to combat oxidative stress, MAAs can protect many marine organisms from the harmful effects of light (Shick and Dunlap 2002). Similarly, mycosporine-glycine showed an additional antioxidant property in coral mucus along with sunscreen, probably protecting endosymbionts from oxidative damage produced through photosynthesis (Teai et al. 1998). Biologically harmful UV rays between 310 and 360 nm are absorbed by MAAs. ...
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Coral mucus secreted by mucocytes provides a protective physicochemical and physiological barrier between coral tissue and external environmental threats. The biomolecules and nutrients of the secreted mucus are derived from endosymbionts, coral polyps and support coral functions, such as feeding, sediment clearing and protection, against numerous biotic and abiotic stressors. The surface mucus layer also houses a diverse community of beneficial microorganisms that defend against pathogens. Enzymes including peptidases, esterases, and glycosidases were observed and described in mucus. Most importantly, the presence of phenoloxidase, an intracellular enzyme in secretory mucus, generally triggers melanin synthesis, providing fast-acting components of invertebrate immunity in disease resistance. However, the purpose and the mechanism of mucus release, effects of mucus components on defense properties, and functional roles in intra- and interspecific interactions are not well described. Thus, the present review aims to understand the mucus components and the complex roles played by mucus in microbial associations, feeding, and resilience that influence coral health.
... The bioactive compounds in coral mucus have been experimentally proven to have antimicrobial activity in the defense against infectious disease by inhibiting Bacillus subtilis, Staphylococcus aureus, Salmonella typhimurium, Vibrio species and Serratia marcescens (Brown and Bythell, 2005, Ritchie, 2006, Bakshani et al., 2018. Besides, Mycosporine-like amino acids (MAA), which act as a sunscreen that absorbs UV radiation (Teai et al., 1998), and phenoloxidase (PO) and melanin activity in mucus of healthy and diseased Pseudodiploria strigosa (Rivera-Ortega and Thome, 2018) have also been described. Prophenoloxidase (ProPO) is a major enzyme of coral innate immunity (Cerenius et al., 2008) which gets upregulated due to oxidative stress. ...
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... Abundance is denoted by intensity of color, ranging from no abundance = white to high abundance = dark green Coral Reefs the microbial structure of our SW samples was influenced by the corals. Mucus shedding is a natural phenomenon in corals (Brown and Bythell 2005) and can be deployed during stressed conditions like increased UV exposure (Teai et al. 1998) and pathogen regulation (Ritchie 2006) but has also been linked to holobiont health via regulation of microbial communities (Glasl et al. 2016). It is possible that exuded dissolved organic matter from the mucus was present in the seawater (Silveira et al. 2017;Weber et al. 2019) and influenced the microbial structure of our SW samples since seawater was collected [ 1 m of the focal corals. ...
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Microbiome studies across taxa have established the influence of host genotype on microbial recruitment and maintenance. However, research exploring host-specific epibionts in scleractinian corals is scant, and the influence of intraspecific differences across environments remains unclear. Here, we studied ten Acropora cervicornis genotypes to investigate the relative roles of host genotype and environment in structuring the epibiome. Coral mucus was sampled in a common garden nursery from replicate ramets of distinct genotypes (T0). Coral fragment replicates (n = 3) of each genotype were then transplanted to nine different field sites in the Lower Florida Keys, and mucus was again sampled one year later from surviving ramets (T12). 16S rRNA amplicon sequencing was used to assess microbial composition, richness, and beta-diversity. The most abundant and consistent amplicon sequencing variants (ASVs) in all samples belonged to Midichloriaceae (MD3-55 genus) and Cyanobacteria (Synechococccus). The relative abundances of these bacterial taxa varied consistently between genotypes, whereas neither the composition nor taxonomic relative abundance were significantly different among field sites. Interestingly, several high MD3-55 hosting genotypes showed rapid diversification and an increase in MD3-55 following transplantation. Overall, our results indicate healthy A. cervicornis genotypes retain distinct epibiome signatures through time, suggesting a strong host component. Lastly, our results show that differences in MD3-55 abundances can be consistently detected in the epibiome of distinct host genotypes of A. cervicornis. As this organism (sensu Aquarickettsia rohweri) has been implicated as a marker of disease resistance, this finding reinforces the potential use of microbial indicators in reef restoration efforts via non-invasive surface/mucus sampling.
... The concentration of MAA in marine organisms is linked with the duration and exposure level of UV radiation (Shick et al. 1995(Shick et al. , 1999Ferrier-Pagès et al. 2007) such as the depth Gleason and Wellington 1995;Shick et al. 1995;Corredor et al. 2000), water motion and photosynthetically active radiation (PAR) (Jokiel et al. 1997). Furthermore, the concentration of MAAs secreted by corals varies with coral species and parts (Teai et al. 1998). Even though many compounds from this class follow Lipinski rule of fives such as mycosporine-Gly, mycosporine-2Gly, palythine (Serine/Thr sulfate/Ser-sulfate), palythinol, and asterina-330, the current results have not used cell cultures nor animal models (with the exception of one study). ...
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