Desmocytes in the calicoblastic epithelium of the stony coral Mycetophyllia reesi and their attachment to the skeleton

Desmocytes scattered over the surface of the corallum of the scleractinian Mycetophyllia reesi attach the calicoblastic tissue to the skeleton. The structure of the desmocyte is generally consistent with that of other scleractinians except for their more rectangular profiles and greater size. However, the extent of attachment is distinctive, and the mode of attachment to mineral is described for the first time. The skeleton contains dual rows of interconnected pits between the septa, within and among which desmocytes form virtually uninterrupted sheets. Desmocytes terminate with hemidesmosomes that attach the epithelium to a fibrillar basal lamina. Fibrils extend from the basal lamina into the skeletal matrix anchoring tissue firmly to the skeleton. In addition, the basal lamina itself appears to be incorporated within the organic matrix during growth, partitioning the skeleton into compartments. Because the skeletal organic matrix is physicochemically labile during demineralization, these intraskeletal details cannot be observed unless polycationic dyes such as Ruthenium red or other glycan precipitating agents are employed in the fixative sequence.     

Gastrodermal structure and feeding responses in the scleractinian Mycetophyllia reesi,a coral with novel digestive filaments

Mycetophyllia reesi Wells is a colonial scleractinian coral whose outer surface consists of a series of oral-pharyngeal openings that lack tentacles. The polyps also lack a column and cannot protrude from the colonial surface. Correspondingly, there is no central digestive cavity. Instead, the pharynx is directly connected to a series of radially arranged mesenterial ducts lying parallel to the skeleton. The ducts, composed primarily of ciliated cells with small mucus inclusions and large, compartmentalized mucocytes, house filaments that protrude through the oral apertures during feeding. The filaments may or may not be directly connected with or originate from the mesenterial ducts and are histologically distinct from them. They are therefore referred to as digestive, rather than mesenterial filaments. In contrast with other scleractinians, the digestive filaments are thin, unequally bilobed stalks with spatulate ends. The cnidoglandular (CG) lobe, the larger of the two, exhibits a distinct cellular zonation. Large mastigophore cnidae and elongated zymogen-like cells are clustered at its distal end. Neither of these cells appear to respond to particulate food material, suggesting that they may be employed in alternative modes of nutrition and/or competition. Behind the distal region, the CG lobe exhibits typical zymogen, mucus, and collar cells as well as numerous atrichous nematocysts. The atrichs and zymogen cells discharge during particulate feeding. Tracts of collar cells with particularly well-defined cilia, elongated rootlets, and mucus inclusions are found at the outer edge of the CG lobe. These cells disgorge their contents during feeding and appear to function in food transport. The smaller lobe of the filament is a muscular sheet containing well-defined fields of circular and longitudinal myofibrils along with associated neurons. Collar cells with lysosome-like inclusions and large, compartmentalized mucocytes are also characteristic of this region. There are no zooxanthellae in the filaments, but these endosymbionts are present as a thin layer in the oral-most portion of the gastrodermis. The cellular zonation and multi-functionality of these digestive filaments suggest another example of a cnidarian structure at the organ level of complexity.     

Feeding behavior,epidermal structure and mucus cytochemistry of the scleractinian Mycetophyllia reesi,a coral without tentacles

The scleractinian Mycetophyllia reesi lacks even the vestiges of tentacles, but quickly captures particulate food by mucus entanglement. Mesenterial filaments emerge through the oral opening, collect the mucus-embedded particulates, and withdraw to the gastrovascular system within 15 min. Mucocytes dominate the outer epidermis with about 3,000 cells/mm(2) and are capable of apocrine discharge en masse. Mucocytes are spumous, typically with web-like inclusions, which for the most part lack electron opacity with ordinary staining, and are only weakly PAS positive. In contrast, the mucus reacts strongly to diamine and other reagents that suggest an appreciable acidic mucopolysaccharide component. The strongest staining reaction occurs in the presence of high iron diamine, suggesting with other tests that the mucus contains significant quantities of sulfated polysaccharides. Cells with cilia anchored by spiriliform microvilli flank the mucocytes and possess small, spumous inclusions that contain acidic, sulfated, and neutral polysaccharides that do not appear to discharge during feeding. These support cells are closely intertwined with narrow, sinuous, secretory cells containing an electron-opaque cytoplasm of unknown composition that is discharged along with mucus during feeding. The outer epidermis also contains scattered cnidae, rather than the clusters or batteries typical of tentacles. The overwhelming abundance of mucocytes is consistent with their importance in feeding. Likewise, the small number of epidermal cnidae suggest they play a minor role in acquiring food. An inner epidermal layer associated with the mesoglea contains epitheliomuscular cells, nerve cells and pigment cells. The two epidermal layers form an essentially pseudostratified, architecturally simple epithelium.     

Morphology of coral desmocytes, cells that anchor the calicoblastic epithelium to the skeleton

 We used light, scanning, and electron microscopy to investigate the ultrastructure of desmocytes in the scleractinian Stylophora pistillata from the Red Sea. Desmocytes are abundant on the calicoblastic epithelium, numbering up to 150 per mm² in the coenosarc. The surface of the skeleton bears shallow pits which may represent desmocyte attachment scars. Previously described as cell remnants or extracellular products, coral desmocytes appear to be bona fide cells as they manifest plasma membranes, organelles, and nuclei. Desmocytes attach to the mesoglea in mortise and tenon fashion. A field of 40 or more tenons protrude fingerlike from the proximal surface of the desmocyte and interdigitate with the mesoglea. Each tenon is coated extracellularly with short fibers which are joined to fibers of the mesoglea. The arrangement resembles previously described “fascial” hemidesmosomes. The short fibers pass through the plasma membrane and connect with relatively long intracellular fibers which occupy the center of each tenon. The long fibers extend distally and attach to structures resembling vertebrate hemidesmosomes. These, in turn, attach to the skeleton. The fiber arrangement and orientation seems designed to resist tensile forces. The dynamic adhesion potentially provided by the distal hemidesmosomes may enable desmocytes to detach and reattach to the skeleton during episodes of mineral accretion. Accepted: 15 April 1997     

Microstructural characteristics of the stony coral genus Acropora useful to coral reef paleoecology and modern conservation

Identification of fossil corals is often limited due to poor preservation of external skeleton morphology, especially in the genus Acropora which is widespread across the Indo‐Pacific. Based on skeleton characteristics from thin section, we here develop a link between the internal skeleton structure and external morphology. Ten characteristics were summarized to distinguish Acropora and five related genera, including the type and differentiation of corallites, the skeleton nature of corallites (septa, columellae, dissepiments, wall), and calcification centers within septa. Acropora is distinctive for its dimorphic corallites: axial and radial. Isopora is similar to Acropora but possess more than a single axial corallites. Montipora and Astreopora (family Acroporidae) have monomorphic corallites and a synapticular ring wall, with clustered calcification center in the former and medial lines in the latter. Pocillopora and Porties are classified by distinctive dissepiments, columellae and septa. These microstructural skeleton characteristics were effective in the genus identification of fossil corals from drilled cores in the South China Sea. Eighteen detailed characteristics (ten of axial corallites, four of radial corallites, and four of coenosteum) were used in the Acropora species classification. The axial corallites size and structure (including corallite diameter, synapticular rings, and septa), the septa of radial corallites, and the arrangement of coenosteum were critical indicators for species identification. This identification guide can help paleoenvironmental and paleoecological analyses and modern coral reef conservation and restoration.     

Association of butterflyfishes and stony coral tissue loss disease in the Florida Keys

Coral Reefs - Since 2014, stony coral tissue loss disease (SCTLD) has rapidly spread throughout the Florida reef tract infecting and killing dozens of coral species. Previous studies have found...     

Nutritional resources as positional information for morphogenesis in the stony coral Stylophora pistillata

We are interested in deciphering the mechanisms for morphogenesis in the Red Sea scleractinian coral Stylophora pistillata with the help of mathematical models. Previous mathematical models for coral morphogenesis assume that skeletal growth is proportional to the amount of locally available energetic resources like diffusible nutrients and photosynthetic products. We introduce a new model which includes factors like dissolved nutrients and photosynthates, but these resources do not serve as building blocks for growth but rather provide some kind of positional information for coral morphogenesis. Depending on this positional information side branches are generated, splittings of branches take place and branch growth direction is determined. The model results are supported by quantitative comparisons with experimental data obtained from young coral colonies.     

Crystallographic evidence for water-assisted photo-induced peptide cleavage in the stony coral fluorescent protein Kaede

A coral fluorescent protein from Trachyphyllia geoffroyi, Kaede, possesses a tripeptide of His62-Tyr63-Gly64, which forms a chromophore with green fluorescence. This chromophore's fluorescence turns red following UV light irradiation. We have previously shown that such photoconversion is achieved by a formal beta-elimination reaction, which results in a cleavage of the peptide bond found between the amide nitrogen and the alpha-carbon at His62. However, the stereochemical arrangement of the chromophore and the precise structural basis for this reaction mechanism previously remained unknown. Here, we report the crystal structures of the green and red form of Kaede at 1.4 A and 1.6 A resolutions, respectively. Our structures depict the cleaved peptide bond in the red form. The chromophore conformations both in the green and red forms are similar, except a well-defined water molecule in the proximity of the His62 imidazole ring in the green form. We propose a molecular mechanism for green-to-red photoconversion, which is assisted by the water molecule.     

Epidermal structure of the scleractinian coral Mycetophyllia ferox: light-induced vesicles,copious mucocytes,and sporadic tentacles

Three colony fragments of the scleractinian coral Mycetophyllia ferox Wells from Florida were observed in flow-through seawater aquaria under light and dark conditions. The colonies were then anesthetized and fixed for microscopic examination. Small vesicles formed across the epidermis in response to light as gastrodermis containing approximately 1.9 × 10⁶ zooxanthellae cm⁻² migrated into them. The vesicles flattened in the dark and the gastrodermis retreated to a clumped position. The epidermis is dominated by mucus cells with more than 6300 per mm². In contrast, there are very few epidermal cnidae. The polyps lack tentacles entirely, though small tentacles do occur, albeit sporadically, along the colline walls. Colline tentacles are expanded both day and night, and there is considerable intracolonial variability in the number of cnidae within them, ranging from as few as 316 to more than 3200 per mm² tentacle. There may be several small cnidocyst batteries containing both spirocysts and nematocysts (all microbasic p-mastigophores), but the principal battery is at the tentacle tip where cnidae are much more densely packed. There is considerable variation in the ratio of the two cnidae among tentacles in the same colony. Since the tentacles occur inconsistently and do not appear to expand, their functional role is unclear. Comparisons of epidermal characters are made with other members of the genus Mycetophyllia.     

Metaproteomics reveals metabolic transitions between healthy and diseased stony coral Mussismilia braziliensis

Infectious diseases such as white plague syndrome (WPS) and black band disease (BBD) have caused massive coral loss worldwide. We performed a metaproteomic study on the Abrolhos coral Mussismilia braziliensis to define the types of proteins expressed in healthy corals compared to WPS‐ and BBD‐affected corals. A total of 6363 MS/MS spectra were identified as 361 different proteins. Healthy corals had a set of proteins that may be considered markers of holobiont homoeostasis, including tubulin, histone, Rab family, ribosomal, peridinin–chlorophyll a‐binding protein, F0F1‐type ATP synthase, alpha‐iG protein, calmodulin and ADP‐ribosylation factor. Cnidaria proteins found in healthy M. braziliensis were associated with Cnidaria–Symbiodinium endosymbiosis and included chaperones (hsp70, hsp90 and calreticulin), structural and membrane modelling proteins (actin) and proteins with functions related to intracellular vesicular traffic (Rab7 and ADP‐ribosylation factor 1) and signal transduction (14‐3‐3 protein and calmodulin). WPS resulted in a clear shift in the predominance of proteins, from those related to aerobic nitrogen‐fixing bacteria (i.e. Rhizobiales, Sphingomonadales and Actinomycetales) in healthy corals to those produced by facultative/anaerobic sulphate‐reducing bacteria (i.e. Enterobacteriales, Alteromonadales, Clostridiales and Bacteroidetes) in WPS corals. BBD corals developed a diverse community dominated by cyanobacteria and sulphur cycle bacteria. Hsp60, hsp90 and adenosylhomocysteinase proteins were produced mainly by cyanobacteria in BBD corals, which is consistent with elevated oxidative stress in hydrogen sulphide‐ and cyanotoxin‐rich environments. This study demonstrates the usefulness of metaproteomics for gaining better comprehension of coral metabolic status in health and disease, especially in reef systems such as the Abrolhos that are suffering from the increase in global and local threatening events.     

The skeletal organic matrix from Mediterranean coral Balanophyllia europaea influences calcium carbonate precipitation

Scleractinian coral skeletons are made mainly of calcium carbonate in the form of aragonite. The mineral deposition occurs in a biological confined environment, but it is still a theme of discussion to what extent the calcification occurs under biological or environmental control. Hence, the shape, size and organization of skeletal crystals from the cellular level through the colony architecture, were attributed to factors as diverse as mineral supersaturation levels and organic mediation of crystal growth. The skeleton contains an intra-skeletal organic matrix (OM) of which only the water soluble component was chemically and physically characterized. In this work that OM from the skeleton of the Balanophyllia europaea, a solitary scleractinian coral endemic to the Mediterranean Sea, is studied in vitro with the aim of understanding its role in the mineralization of calcium carbonate. Mineralization of calcium carbonate was conducted by overgrowth experiments on coral skeleton and in calcium chloride solutions containing different ratios of water soluble and/or insoluble OM and of magnesium ions. The precipitates were characterized by diffractometric, spectroscopic and microscopic techniques. The results showed that both soluble and insoluble OM components influence calcium carbonate precipitation and that the effect is enhanced by their co-presence. The role of magnesium ions is also affected by the presence of the OM components. Thus, in vitro, OM influences calcium carbonate crystal morphology, aggregation and polymorphism as a function of its composition and of the content of magnesium ions in the precipitation media. This research, although does not resolve the controversy between environmental or biological control on the deposition of calcium carbonate in corals, sheds a light on the role of OM, which appears mediated by the presence of magnesium ions.     

Genetic basis of stony coral biomineralization: History,trends and future prospects

Despite their simple body plan, stony corals (order Scleractinia, phylum Cnidaria) can produce massive and complex exoskeletal structures in shallow, tropical and subtropical regions of Earth’s oceans. The species-specific macromorphologies of their aragonite skeletons suggest a highly coordinated biomineralization process that is rooted in their genomes, and which has persisted across major climatic shifts over the past 400 + million years. The mechanisms by which stony corals produce their skeletons has been the subject of interest for at least the last 160 years, and the pace of understanding the process has increased dramatically in the past decade since the sequencing of the first coral genome in 2011. In this review, we detail what is known to date about the genetic basis of the stony coral biomineralization process, with a focus on advances in the last several years as well as ways that physical and chemical tools can be combined with genetics, and then propose next steps forward for the coming decade.     

Grazing by a small fish affects the early stages of a post-settlement stony coral

Short-term experiments were used to isolate the detrimental effects of grazer disturbance on young corals, and determine the stage of development at which recruits are no longer susceptible to this disturbance. Artificial substrata containing an algal matrix and coral recruits of different life stages were exposed to grazing by epilithic algal matrix (EAM) feeding combtoothed blennies, Salarias fasciatus. Single polyp recruits were vulnerable to grazer disturbance, while multi-polyp recruits (ca. 6–8 polyps) survived with evidence of minor damage in the form of tissue and polyp loss. The result indicates that blennies, although small and possessing weak dentition, can negatively influence the survival of young coral recruits. The protruding structure of micro-nubbins, representing juvenile corals were not damaged, suggesting that coral achieving that size and form can escape such damage. Communicated by Ecology Editor Prof. Peter Mumby     

Testicular somatic cells in the stony coral Euphyllia ancora express an endogenous green fluorescent protein

In a variety of organisms, adult gonads contain several specialized somatic cells that regulate and support the development of germline cells. In stony corals, the characteristics and functions of gonadal somatic cells remain largely unknown. No molecular markers are currently available that allow for the identification and enrichment of gonadal somatic cells in corals. Here, we showed that the testicular somatic cells of a stony coral, Euphyllia ancora, express an endogenous green fluorescent protein (GFP). Fluorescence microscopy showed that, in contrast to the endogenous expression of the red fluorescent protein of E. ancora ovaries that we have previously reported, the testes displayed a distinct green fluorescence. Molecular identification and spectrum characterization demonstrated that E. ancora testes expressed a GFP (named EaGFP) that is a homolog of the GFP from the jellyfish Aequorea victoria and that possesses an excitation maximum of 506 nm and an emission maximum of 514 nm. Immunohistochemical analyses revealed that the testicular somatic cells, but not the germ cells, expressed EaGFP. EaGFP was enclosed within one or a few granules in the cytoplasm of testicular somatic cells, and the granule number decreased as spermatogenesis proceeded. We also showed that testicular somatic cells could be enriched by using endogenous GFP as an indicator. The present study not only revealed one of the unique cellular characteristics of coral testicular cells but also established a technical basis for more in‐depth investigations of the function of testicular somatic cells in spermatogenesis in future studies.     

Crystallographic and chemical signatures in coral skeletal aragonite

Coral Reefs - Corals nucleate and grow aragonite crystals, organizing them into intricate skeletal structures that ultimately build the world’s coral reefs. Crystallography and chemistry have...     

Computerized tomography and skeletal density of coral skeletons

In this paper I describe and discuss the use of medical X-ray computerized tomography (CT) in the study of coral skeletons. CT generates X-ray images along freely chosen sections through the skeleton and offers, as well, the possibility of density measurements based on X-ray attenuation. This method has been applied to measure the skeletal density of the Caribbean reef-building coral Montastrea annularis, from Curaçao, Netherlands Antilles. The observed, non-linear increase of skeletal density with depth can be attributed to decreasing photo-synthetic rates with increasing water depth. A comparison with extension rate measurements shows the inverse relationship between extension rate and skeletal density. CT proves to be aquick and non-destructive method to reveal growth structures (density banding) since it measures skeletal density.     

A fluorescent variant of a protein from the stony coral Montipora facilitates dual-color single-laser fluorescence cross-correlation spectroscopy

Dual-color fluorescence cross-correlation spectroscopy (FCCS) is a promising technique for quantifying protein-protein interactions. In this technique, two different fluorescent labels are excited and detected simultaneously within a common measurement volume. Difficulties in aligning two laser lines and emission crossover between the two fluorophores, however, make this technique complex. To overcome these limitations, we developed a fluorescent protein with a large Stokes shift. This protein, named Keima, absorbs and emits light maximally at 440 nm and 620 nm, respectively. Combining a monomeric version of Keima with cyan fluorescent protein allowed dual-color FCCS with a single 458-nm laser line and complete separation of the fluorescent protein emissions. This FCCS approach enabled sensitive detection of proteolysis by caspase-3 and the association of calmodulin with calmodulin-dependent enzymes. In addition, Keima and a spectral variant that emits maximally at 570 nm might facilitate simultaneous multicolor imaging with single-wavelength excitation.