Intercellular Attachment in the Epithelium of Hydra As Revealed by Electron Microscopy

In Hydra adjacent epithelial cells are bound firmly to each other by desmosomes of a type not described in detail hitherto. The most prominent feature of these desmosomes is the presence of a series of parallel lamellae which bridge the intercellular space and connect the two apposed cell surfaces directly. These structures, here termed intercellular attachment lamellae, display two peaks of density about 50 A apart. These dense lines appear in some instances to be continuous with the outer dense components of the plasma unit membranes of the attached cells. The presence of prominent lamellae in intercellular attachments is sufficiently distinctive to deserve special terminology; accordingly, the term septate desmosome is proposed. It is noted that septate desmosomes may have been seen in other animals in instances where published electron micrographs show cross-striations or prominent connections in regions of intercellular attachment. It is suggested that septate desmosomes in Hydra, in addition to binding cells firmly to each other, form barriers to the movement of water into intercellular spaces and thus help to protect the organism's internal environment. Observations on the use of phosphotungstic acid for improving contrast in materials embedded in epoxy resins are also recorded.     

THE STRUCTURAL ORGANIZATION OF THE SEPTATE AND GAP JUNCTIONS OF HYDRA

The septate junctions and gap junctions of Hydra were studied utilizing the extracellular tracers lanthanum hydroxide and ruthenium red. Analysis of the septate junction from four perspectives has shown that each septum consists of a single row of hexagons sharing common sides of 50–60 A. Each hexagon is folded into chair configuration. Two sets of projections emanate from the corners of the hexagons. One set (A projections) attaches the hexagons to the cell membranes at 80–100-A intervals, while the other set (V projections) joins some adjacent septa to each other. The septate junctions generally contain a few large interseptal spaces and a few septa which do not extend the full length of the junction. Basal to the septate junctions the cells in each layer are joined by numerous gap junctions. Gap junctions also join the muscular processes in each layer as well as those which connect the layers across the mesoglea. The gap junctions of Hydra are composed of rounded plaques 0.15–0.5 µ in diameter which contain 85-A hexagonally packed subunits. Each plaque is delimited from the surrounding intercellular space by a single 40-A band. Large numbers of these plaques are tightly packed, often lying about 20 A apart. This en plaque configuration of the gap junctions of Hydra contrasts with their sparser, more widely separated distribution in many vertebrate tissues. These studies conclude that the septate junction may possess some barrier properties and that both junctions are important in intercellular adhesion. On a morphological basis, the gap junction appears to be more suitable for intercellular coupling than the septate junction.     

CELL JUNCTIONS IN AMPHIBIAN SKIN

Cell junctions have been investigated in the amphibian epidermis, a stratified squamous epithelium, and compared to those described previously in simple columnar epithelia of mammalian cavitary organs. In adult frogs and toads, and in larvae approaching metamorphosis, belts of membrane fusion or zonulae occludentes of considerable depth are regularly found between adjoining cells of the outermost layer of the stratum corneum, binding the cells together into a continuous, uninterrupted sheet. Another set of occluding zonules appears in the second cornified layer (when such a layer is present), and a third set usually occurs in the outermost layer of the stratum granulosum. Specialized elements described as "modified" and "composite" desmosomes are encountered along the lateral and basal aspects, respectively, of the cornified cells; ordinary desmosomes and maculae occludentes (i.e., spots of membrane fusion) are found in all other strata. The usual 200 A intercellular gap is generally maintained between the cells of the stratum germinativum at the basal ends of the intercellular spaces. Hence, the intercellular spaces of the epidermis form a largely continuous network, closed to the external medium and open to the dermal interstitia. The situation is comparable to that found in columnar epithelia, except that the intercellular spaces are much more extensive, and an extracellular subcompartment (or two) apparently exists in the stratum corneum and between the latter and the stratum granulosum. The last subcompartment is usually filled with a dense substance, probably derived from discharged secretory granules. The tripartite junctional complex characteristic of lumen-lining epithelia (i.e., a zonula occludens followed by a zonula adhaerens, and desmosome) is seen only in early larvae; in adults and in larvae approaching metamorphosis, the occluding zonule is followed directly by a series of modified desmosomes. Interpreted in the light of current physiological data, these findings suggest that the diffusion of water, ions, and small, water-soluble molecules is impeded along the intercellular spaces of the epidermis by zonulae occludentes while it is facilitated from cell to cell within the epidermis by zonulae and maculae occludentes.     

Electrical properties of the body wall of Hydra

If the hydrostatic pressure in the enteron of Hydra is made more than 2–4 mm of water greater than the outside pressure, the animal becomes distended, indicating that the normal enteron pressure is less than this. Positive enteron pressure attenuates the spontaneous, negative-going electrical spikes across the body wall, which are called contraction pulses (CP''s) because of their relation to column contraction. Pressure has little effect on the transepithelial resting potential. The low frequency electrical impedance of the column is nonlinear. The impedance tends to increase as the transepithelial potential is made more negative. The nonlinearity has both initial and delayed components. The DC impedance of the column near the resting potential averages 100 kohms (approximately 5 kohms-cm²). The phase between transepithelial potential and imposed sinusoidal current approaches -90° with increasing current frequency. Bode plots of the column impedance and the phase lag indicate that the column has three or more time constants. CP''s show several unusual features: (a) their amplitude and frequency are essentially independent of the transepithelial potential when the latter is altered by imposed current; (b) there is practically no change in column impedance during CP firing; (c) when the transepithelial potential is clamped at zero, CP''s continue to appear spontaneously as current spikes. These features are consistent with the hypothesis that the CP-generating membrane forms but a small fraction of the total transverse impedance of the column.     

A STUDY OF THE FINE STRUCTURE OF THE EPIDERMIS OF RANA PIPIENS

The epidermis of adult Rana pipiens has been studied by electron microscopy and histological and histochemical methods. It was found that the epidermis is engaged in the production of both keratin and mucus. The basal cells are mainly filled with tonofilaments, whereas the cells located in the mid-portion of the epidermis contain both tonofilaments and mucous granules. Golgi vesicles and endoplasmic reticulum are found in relative abundance in the mucus-producing cells and seem to be involved in the production of mucous granules. The mucus seen was partly retained within the cells and partly secreted into the intercellular spaces. The outermost keratinized cells contain mainly filaments and a few remnants of cell constituents.     

ADENOSINE TRIPHOSPHATASE LOCALIZATION IN AMPHIBIAN EPIDERMIS

The localization of ATPase¹ activity has been studied by light and electron microscopy in the epidermis of Rana pipiens, Rana catesbiana, and Bufo marinus. The reaction was carried out on skin (glutaraldehyde-fixed or fresh) sectioned with or without freezing. Best results were obtained with nonfrozen sections of fixed tissue. The incubation mixture was either a Wachstein-Meisel medium, or a modification which approximates assay systems used in biochemical studies of transport ATPases. The reaction product was found localized in contact with the outer leaflet of all cell membranes facing the labyrinth of intercellular spaces of the epidermis. It was absent from: (a) membrane areas involved in cell junctions (desmosomes, zonulae and maculae occludentes); (b) cell membranes facing the external medium (i.e., those on the distal aspect of the ultimate cell layer in s. corneum); (c) cell membranes facing the dermis (those on the proximal aspect of cells in s. germinativum). In the presence of (Na⁺ + K⁺) the localization did not change, but the reaction was not appreciably activated. A similar though less intense reaction was obtained with ITP, but not with ADP, AMP, and GP as substrates. The results are discussed in relation to available data on transport ATPases in general, and on the morphology and physiology of amphibian skin in particular. Assuming that the ATPase studied is related to transport ATPase, the findings suggest a series of modifications to the frog skin model proposed by Koefoed-Johnsen and Ussing. The salient feature of this modified model is the localization of the Na⁺ pump along all cell membranes facing the intercellular spaces of the epidermis.     

Fine structure of supporting cells in the lateral-line canal-organ of Fundulus

Phase and electron microscopic studies have revealed that the supporting cells of the lateral-line canal-organ of Fundulus heteroclitus have a fine structure characterized by (1) mitochondria and vacuoles in the apical zone, (2) granular endoplasmic reticulum surrounding a core of Golgi complex in the middle zone, and (3) an indented nucleus in the basal zone. In the middle and basal zones, wide intercellular spaces separate the adjacent supporting cells, whose plasma membranes form long flap-like interdigitations across the intercellular spaces. Secretion of subcupular fluid and cupula, metabolic regulation through the intercellular spaces, and rigid support for the organ are discussed as possible metabolic and mechanical functions of the supporting cells essential for the lateral-line canal-organ.     

Colleters in Bathysa cuspidata (Rubiaceae): Development,ultrastructure and chemical composition of the secretion

This paper describes the development of colleters of Bathysa cuspidata, Rubiaceae, considering anatomical, histochemical and ultrastructural aspects and going from first differentiation stages until senescence. Further, the chemical composition of the secretion is investigated. The samples were prepared according to the usual techniques for light microscopy and scanning and transmission electron microscopy. Electrophoresis and thin layer chromatography (TLC) were used to confirm the results obtained in the histochemical tests. The colleters occur at the ventral surface of the stipules which protect the leaf primordia as well as the shoot meristem. The origin of the colleters is mixed, involving protoderm and ground meristem. The Bathysa colleters are of the standard type or are bifurcated; this latter type is documented here for the first time for Rubiaceae. Colleter secretion is a mucilage rich in protein, as determined by histochemical tests and confirmed by chemical analysis. Phenolic compounds and terpenes were detected only in the colleters themselves, but not in the secretion. The epithelial cells present conspicuous nuclei and nucleoli and the cytoplasm is rich in dictyosomes, endoplasmic reticulum, mitochondria, vesicles and small vacuoles with a fibrillar content. The accumulation of phenolic compounds and terpenes, the formation of a large central vacuole, the increase of the intercellular and subcuticular spaces occupied by the secretion and, finally, the darkening and the wilting of the colleters characterize the senescence of these structures. The secretion process of the colleters of B. cuspidata suggests a process of programmed cell death.     

Response of the seminiferous epithelium of the rat testis to withdrawal of androgen: evidence for direct effect upon intercellular spaces associated with Sertoli cell junctional complexes

The morphological response of the Sertoli cells to partial or complete withdrawal of testosterone was studied in adult rats following hypophysectomy or administration of ethane dimethanesulphonate (EDS), a toxicant known to destroy selectively the Leydig cells of the testis. To assess the role of germ cells in effecting changes to Sertoli cells following withdrawal of testosterone, germ cell-deficient rats with Sertoli-cell-only testes (SCO) were treated with EDS to remove the source of testosterone. At 6 days after hypophysectomy or 4,6 and 8 days after EDS treatment, stage VII and VIII seminiferous tubules showed degenerating germ cells and numerous basally-located vacuoles approximately 1–15 m in diameter. Ultrastructural analysis indicated that most of the vacuoles were multiple focal dilations of the intercellular space associated with Sertoli cell junctional complexes. In SCO rats, treatment with EDS resulted in a significant (P<0.05) increase in the formation of many vacuoles particularly in the base but also in the trunk of the Sertoli cells and again electron microscopic analysis showed multiple, localized expansions of the intercellular space associated with Sertoli cell junctional complexes. The appearance of intercellular spaces in SCO testes following androgen withdrawal cannot be attributed to shrinkage of degenerating germ cells since the seminiferous tubules did not contain germ cells. It is concluded that withdrawal of androgen induces early morphological alterations of the Sertoli cell junctional complexes in which the sites of membrane fusions representing tight junctions remain intact whereas the intercellular spaces exhibit major focal dilations. The results are discussed in relation to the fluid secretion by the seminiferous tubules which is regulated by the Sertoli cells.     

Formation of intercellular gas space in the diaphragm during the development of aerenchyma in the leaf petiole of Sagittaria trifolia

The development of aerenchyma in the petiole of Sagittaria trifolia L. was studied by means of light-microscopy, scanning electron microscope, transmission electron microscope and immunofluorescence, focusing on the formation of intercellular spaces in diaphragms and its relationship with the organization of cortical microtubule arrays. A complex and organized honeycomb-like schizogenous aerenchyma formed by cylinders and vascular diaphragms was observed in the petiole of S. trifolia at different developmental stages. Cell division was the primary factor contributing to the increased volume of air spaces at early stages, while cell enlargement became the primary factor at later stages. The cortical microtubules localize at the sites where intercellular spaces and the secondary cell walls will be formed or deposited during the formation of intercellular spaces by the separation of diaphragm cells. Cortical microtubules were observed at the boundary of diaphragm cells and the fringes of intercellular spaces at later developmental stages where cell expansion occurs rapidly. These observations support the hypothesis that reorganization of cortical microtubule arrays might be related to the formation of air spaces in diaphragms and are involved in the deposition of secondary cell walls.     

The fine structure of epidermal papillae of Travisia forbesii (Annelida)

The structure of the epidermis of Travisia forbesii was described using light and electron microscopy. The epidermis is a highly modified variant of the normal one-layer polychaete epithelium. It consists of basal epidermal cells and an external layer of closely sited papillae consisting of glandular and supportive epidermal cells, and extensive electron-transparent intercellular spaces. The papillae are embedded in the thick cuticle. Each papilla has a peduncle, which is formed by one cell that penetrates the inner cuticle layer to the basal epidermal cells. A fold of basement membrane forms the core of the peduncle and ends in the base of a papilla. All epidermal cells are connected to each other with apical cell junctions and to the basement membrane with hemidesmosomes, so the epithelium is continuous and uninterrupted. The epidermis has an intra-epidermal neuron plexus. The structure of the papillae is compared with papillae and tubercles of other polychaetes, and the possible functional significance and phylogenetic implications of these structures are discussed.     

Intercellular Sodium Regulates Repolarization in Cardiac Tissue with Sodium Channel Gain of Function

In cardiac myocytes, action potentials are initiated by an influx of sodium (Na⁺) ions via voltage-gated Na⁺ channels. Na⁺ channel gain of function (GOF), arising in both inherited conditions associated with mutation in the gene encoding the Na⁺ channel and acquired conditions associated with heart failure, ischemia, and atrial fibrillation, enhance Na⁺ influx, generating a late Na⁺ current that prolongs action potential duration (APD) and triggering proarrhythmic early afterdepolarizations (EADs). Recent studies have shown that Na⁺ channels are highly clustered at the myocyte intercalated disk, facilitating formation of Na⁺ nanodomains in the intercellular cleft between cells. Simulations from our group have recently predicted that narrowing the width of the intercellular cleft can suppress APD prolongation and EADs in the presence of Na⁺ channel mutations because of increased intercellular cleft Na⁺ ion depletion. In this study, we investigate the effects of modulating multiple extracellular spaces, specifically the intercellular cleft and bulk interstitial space, in a novel computational model and experimentally via osmotic agents albumin, dextran 70, and mannitol. We perform optical mapping and transmission electron microscopy in a drug-induced (sea anemone toxin, ATXII) Na⁺ channel GOF isolated heart model and modulate extracellular spaces via osmotic agents. Single-cell patch-clamp experiments confirmed that the osmotic agents individually do not enhance late Na⁺ current. Both experiments and simulations are consistent with the conclusion that intercellular cleft narrowing or expansion regulates APD prolongation; in contrast, modulating the bulk interstitial space has negligible effects on repolarization. Thus, we predict that intercellular cleft Na⁺ nanodomain formation and collapse critically regulates cardiac repolarization in the setting of Na⁺ channel GOF.     

Fine structure of the rectal pads in Grylloblatta compodeiformis (walker) (Orthoptera : Grylloblattidae) with reference to fluid transport

The rectal pads of the primitive insect Grylloblatta compodeiformis (Orthoptera : Grylloblattidae) were studied using light and electron microscopy. In this species, the rectal epithelium is thickened to form 6 prominent rectal pads, each of which is composed of tall columnar epithelial cells and laterally placed slender junctional cells, but is devoid of secondary cells. The rectal pads are interconnected by simple rectal epithelium, and are lined by a thin cuticular intima. They are surrounded by an extensive connective tissue space, which contains bundles of delicate connective tissue fibers, neurosecretory axons, and tracheae and tracheoles, which do not penetrate into the pads. The epithelial cells exhibit extensive infoldings of the apical plasma membranes that are closely associated with mitochondria. The lateral membranes are also highly folded around large mitochondria that possess longitudinally oriented cristae. These membrane folds form mitochondrial-scalariform junctional complexes and enclose intercellular channels and spaces. The apical cytoplasm of the epithelial cells contains numerous coated vesicles, dense tubular elements, multivesicular bodies and lysosomes, which suggests receptor-mediated endocytosis of macromolecules. The presence of large whorls of rough endoplasmic reticulum and abundant free ribosomes in the cytoplasm and nuclei with multiple, well-developed nucleoli indicate that the epithelial cells are actively engaged in protein synthesis. The ultrastructural features were examined in relation to their role in fluid transport in a cold habitat.     

LEAF ANATOMY OF TISSUE-CULTURED LIQUIDAMBAR STYRACIFLUA (HAMAMELIDACEAE) DURING ACCLIMATIZATION

Structural changes accompanying the acclimation process were observed in leaves of sweetgum, Liquidambar styraciflua, using light and transmission electron microscopy (TEM). Comparisons were made of leaves obtained from tissue culture, plantlets acclimated after transfer from the in vitro environment to soil, and field grown trees. Leaves of cultured plantlets lacked a differentiated palisade parenchyma and had spongy parenchyma interspersed with large air spaces. Field grown leaves showed distinct palisade and spongy tissues and a high cell density. New leaves from acclimated plantlets showed an elongation of the upper mesophyll with fewer intercellular spaces than cultured plants. Cells from leaves from in vitro plantlets had large vacuoles, limited cytoplasmic content and flattened chloroplast with an irregularly arranged internal membrane system. Acclimated and field leaf cells had a greater cytoplasmic content than cultured leaves, with the former having more dominate vacuoles. Chloroplasts had evident grana. Acclimated and field leaves had a well developed cuticle unlike leaves from culture.     

Diffusion resistances between ADH-induced vacuoles and the extracellular space in rabbit collecting duct: evidence that mos vacuoles are intracellular,endocytic compartments

Summary Large vacuoles form in the renal collecting duct following the onset of antidiuretic hormone (ADH)-stimulated water reabsorption. The aim of the present study was to test two alternative hypotheses regarding the origins of these structures: (1) the vacuoles constitute basilar, extracellular spaces that dilate as water flows through these spaces from cells into the peritubular compartment; or (2) the vacuoles represent intracellular, endocytic compartments that dilate during water reabsorption due to enhanced fluid phase endocytosis. Fluorescence-digital imaging microscopy was used to visualize the uptake into vacuoles of a hydrophilic fluorochrome (6 methoxy-N-[3 sulfopropyl] quinolinium) whose fluorescence is markedly quenched by halides. During their formation, most vacuoles (67%) accumulated the fluorochrome from the peritubular bath and trapped the dye well after (>60 min) washing it from the bath. The spatial pattern of fluorescence within individual vacuoles indicated that the dye was trapped within these structures as a fluid-phase marker and was not bound to the vacuole margins. The fluorescence of dye trapped within vacuoles was virtually unaltered by changes in peritubular Cl^- or Br^- concentration that elicit dramatic quenching of dye-fluorescence in bulk solution, as expected if there exists a high diffusion resistance between the interiors of these structures and the peritubular space. These results indicate that most ADH-induced vaculles represent endocytic compartments that are not directly connected to the extracellular space.     

Silicon Storage in Selected Dicotyledons

Silicon was localized in some dicotyledons (Minuartia verna, Silene cucubalus, Thlaspi coerulescens, Viola calaminaria, Nicotiana tabacum, Pisum sativum) by analytical transmission electron microscopy as apoplastic crystalline inclusions of SiO₂ in intercellular spaces of the leaf parenchyma, between cell wall and plasma membrane and inside the vacuoles. Ca-silicate, and in some plants Sn-silicate, forms the peripheral parts of the crystalline inclusions. These unstable compounds are converted spontaneously in the plant cells into the more stable SiO₂, which forms the central part of all crystalline inclusions. The function of silicon in these plants is discussed.     

Dianthus caryophyllus stems and Zantedeschia aethiopica petioles/pedicels show anatomical features indicating efficient photosynthesis

The fine structure of the green stem of Dianthus caryophyllus, the leaf petiole and the flower pedicel of Zantedeschia aethiopica were studied using light and scanning electron microscopy. It was revealed that these non-foliar plant parts of both species possess epidermis with numerous stomata. Stomatal density of D. caryophyllus stem was found to be relatively high (79 vs 100 per mm² found on leaf surface). Z. aethiopica petioles and pedicels also possess numerous stomata (17 per mm²), yet stomatal density was found to be about half of that of leaves. Anatomical differences observed between petioles and pedicels were only minor. Stems of D. caryophyllus as well as petioles and pedicels of Z. aethiopica have a chlorenchyma-type tissue whose fine structure is quite similar to the leaf palisade chlorenchyma. Yet, the palisade of Z. aethiopica petioles and pedicels shows a peculiar arrangement: palisade cells are arranged with their long axis parallel to the longitudinal organ axis. Palisade tissue found in the aforementioned non-foliar plant organs in both species shows strong red chlorophyll auto-fluorescence under epi-fluorescence optics, consists of cells with abundant chloroplasts, possesses high percentage of intercellular spaces (13 and 20%, respectively) and its cells expose considerable part of their surface to the intercellular air. The fine structure of this stem palisade tissue along with the abundance of functional stomata found on the epidermis may support efficient photosynthesis.     

Book lung development in juveniles and adults of the cobweb spider, Parasteatoda tepidariorum C. L. Koch, 1841 (Araneomorphae,Theridiidae)

Light and transmission electron microscopy were used to study the development of new book lung lamellae in juvenile and adult spiders (Parasteatoda tepidariorum). As hypothesized earlier in a study of embryos, mesenchyme cells dispersed throughout the opisthosoma (EMT) are a likely source of precursor epithelial cells (MET) for the new lamellae. The precursor cells in juveniles and adults continue many of the complex activities observed in embryos, e.g., migration, alignment, lumen formation, thinning, elongation, and secretion of the cuticle of air channel walls and trabeculae. The apicobasal polarity of precursor cells for new channels is apparently induced by the polarity pattern of precursor cells of channels produced earlier. Thus, new air and hemolymph channels extend and continue the alternating pattern of older channels. At sites more distant from the spiracle and atrium, new channels are usually produced by the mode II process (intracellular alignment and merging of vesicles). These air channels have bridging trabeculae and are quite stable in size throughout their length. At sites closer to the spiracle and atrium, new channels may be produced by mode I (coalescence of merocrine vesicle secretion). This raises the hypothesis that structural and functional differences in mode I and II channels and differing oxygen and fluid conditions with distance from the spiracle and atrium determine the mode of formation of new channels. Observations herein support an earlier hypothesis that there is some intercellular apical/apical and basal/basal affinity among the opposed surfaces of aligned precursor cells. This results in the alternating pattern of air channels at the apical and hemolymph channels at the basal cell surfaces.     

Fine structural basis of the cutaneous water barrier in nestling Zebra Finches Poephila guttata

Transepidermal water loss was studied in nestlings, fledglings and adults of the xerophylic Zebra Finch Poephila guttata. Nestlings lose little water (2–4 ppm/0–5 cm²/h) through the skin as compared to adults (60–70 ppm/0–5 cm²/h). Light and electron microscopic examination of the skin sections of both age classes revealed an abundance of lipids in the form of vacuoles and large multigranular bodies in the epidermis of nestlings, but few such lipid bodies in the epidermis of adults. Some of the disc-like contents of granular bodies appear to be extruded into the intercellular spaces. Based on earlier studies with mammals and reptiles, it is concluded that epidermal lipids are the basis of the integumentary permeability barrier in nestlings.     

Histological alterations and microbial ecology of the intestine in gilthead seabream (Sparus aurata L.) fed dietary probiotics and microalgae

The effects on histology and microbial ecology in gilthead seabream (Sparus aurata) intestine caused by dietary probiotic and microalgae were studied. Fish were fed non-supplemented (C, control) or supplemented diets with Tetraselmis chuii, Phaeodactylum tricornutum and Bacillus subtilis single or combined (diets T, P, B, BT and BP) for 4?weeks. Curiously, fish fed the experimental diets showed similar morphological alterations when studied by light and electron microscopy and significant signs of intestinal damage were detected. No effect of microalgae or B. subtilis on the intestinal absorptive area was observed, whereas the number of goblet cells and IELs were significantly lower in fish fed the T, P, B and BT diets and T, BT and BP diets, respectively. Interestingly, only the diets containing B. subtilis resulted in a significant reduction of microvilli height. Alterations such as wide intercellular spaces and large vacuoles in enterocytes were observed in fish fed T, B, BT, BT and P in lesser degrees. These observations demonstrate that fish fed experimental diets presented different signs of oedema and inflammation that could compromise their body homeostasis. Moreover, the experimental diets cause important alterations in the intestinal microbiota by a significant decrease in bacterial diversity, as demonstrated by the fall in specific richness, Shannon and range-weighted richness indices. To our knowledge, this is the first in vivo study regarding the implications of the use of probiotics in combination with immunostimulants on fish intestinal morphology and microbiota. More morphofunctional studies are needed in order to correlate the nutritional and immune aspects of fish gut.