Electron microscopical localization of chitin in the cuticle of Halicryptus spinulosus and Priapulus caudatus (Priapulida) using gold-labelled wheat germ agglutinin: phylogenetic implications for the evolution of the cuticle within the Nemathelminthes

 The ultrastructure of the cuticle of adult and larval Priapulus caudatus and Halicryptus spinulosus is investigated and new features of cuticle formation during moulting are described. For the localization of chitin by TEM wheat germ agglutinin coupled to colloidal gold was used as a marker. Proteinaceous layers of the cuticle are revealed by digestion with pronase. The cuticle of larval and adult specimens of both species consists of three main layers: the outer, very thin, electron-dense epicuticle, the electron-dense exocuticle and the fibrillar, electron-lucent endocuticle. Depending on the body region, the exocuticle comprises two or three sublayers. The endocuticle can be subdivided into two sublayers as well. In strengthened parts such as the teeth, the endocuticle becomes sclerotized and appears electron-dense. Only all endocuticular layers show an intense labelling with wheat germ agglutinin-gold conjugates in all investigated specimens. Additional weak labelling is observed in the exocuticle III layer of the larval lorica of P. caudatus. All other cuticular layers remain unlabelled. Chitinase dissolves the unsclerotized endocuticular layers almost completely, but also exocuticle II and partly the loricate exocuticle III. The epicuticle, the homogeneous exocuticle I and the sclerotized endocuticle are not affected by chitinase. The labelling is completely prevented in all layers after incubation with chitinase. Pronase dissolves all exocuticular layers, but not evenly. The presumably sclerotized regions of exocuticle I are not affected as well as the complete epicuticle and the endocuticle. All cuticular features of the Priapulida are compared with the cuticle of each high-ranked taxon within the Nemathelminthes with special regard to the occurrence of chitin. Based on this out-group comparison it can be concluded that: (1) a two-layered cuticle with a trilaminate epicuticle and a proteinaceous basal layer represents an autapomorphic feature of the Nemathelminthes, (2) the stem species of the Cycloneuralia have already evolved an additional basal chitinous layer, (3) such a three-layered cuticle is maintained as a plesiomophy in the ground pattern of the Scalidophora and (4) in the Nematoida, the chitinous basal layer is replaced by a collagenous one at least in the adults; the synthesis of chitin is restricted to early developmental phases or the pharyngeal cuticle. Accepted: 12 March 1998     

The fine structure and deposition of the larval cuticle of the sheep blowfly (Lucilia Cuprina)

The cuticle of Lucilia is composed of an untanned endocuticle and a complex epicuticle of four layers, superficial layer, outer epicuticle, cuticulin and dense layer. The outer epicuticle and attached epicuticular filaments are resistant to acid hydrolysis. During deposition of the cuticle of each larval instar, the cuticulin and dense layers are formed first, followed by the outer epicuticle, which appears to be laid down by secretions from the epidermis passing through the cuticulin via epicuticular filaments. The outer epicuticle is found in the position normally occupied by the wax layer of other insect species.     

Structure of the cuticle of the common house cricket with reference to the location of lipids

Cuticle segments from the thorax, abdomen, and jumping legs of the house cricket. Acheta domesticus, were examined using histological techniques for light microscopy, scanning and transmission electron microscopy, and direct examination of frozen-fractured cuticle. The surface of untreated cuticle is covered by a lipid film which obscures fine surface detail. Standard EM preparative procedures, as well as washing the cuticle with ethanol before examination, remove this film exposing previously covered openings to dermal gland ducts and wax canals. An epicuticle, exocuticle, mesocuticle, endocuticle, and a deposition layer were present in all transverse sections of cuticle. Light microscopy showed that the exocuticle and mesocuticle are heavily impregnated with lipids, whereas there is little lipid associated with the endocuticle. Frozen-fractured cuticle clearly shows the ‘plywood’ structure of the meso- and endocuticle, while the exocuticle fractures as if it were a solid sheet. The epicuticle is composed of a dense homogeneous layer, cuticulin, outer epicuticle, and the outer membrane. Superficial wax was detected only in cuticle samples prepared using vinylcyclohexane dioxide as a polar dehydrant. The results were used to construct a comprehensive model of the cuticle of A. domesticus.     

Cuticle secretion during larval growth in Drosophila melanogaster

The moulting cycle and growth of the larval integument of Drosophila melanogaster has been studied by light and electron microscopy. Growth during the first, second and third larval instars is accompanied by 3.0-, 3.4- and 3.7-fold increases in surface area, respectively. Growth in surface area occurs continuously during the larval stages, with no detectable relationship to the moulting cycle. Measurements of the thickness of the cuticular layers show that the endocuticle grows in thickness by apposition and in surface area by stretching. The pre-apolytic epicuticle remains at fairly constant thickness during the increase in surface area, indicating that it grows by intussusception of new components. Post-apolytic epicuticle becomes thinner and increases in surface area by stretching. The epicuticle and pre-ecdysial endocuticle are traversed by filaments, but these do not penetrate the endocuticle secreted after ecdysis. We suggest that the filaments transport breakdown products from the old cuticle inward to the epidermis for reutilization. The growth and deposition of cuticle in two larval growth mutants, lethal (2) giant larvae and Chubby Tubby, involves mechanisms similar to those found in wild-type larvae, but in Chubby Tubby the endocuticle contains inclusions which are ultrastructurally similar to dense epicuticle.     

Ultrastructure and cuticle formation of the carapace in the myodocopan ostracod exemplified by Euphilomedes japonica (Crustacea: Ostracoda)

The ultrastructure and formation of the cuticle of a myodocopan ostracod, Euphilomedes japonica, are investigated utilizing scanning and transmission electron microscopy. The outer lamella cuticle consists of four layers; epicuticle, exocuticle, endocuticle, and membranous layer like in the cuticle of other arthropods. The exocuticle and endocuticle are well-calcified and the organic matrix develops within the both cuticles. The outermost layer of new cuticle (epicuticle) is secreted first and the inner layers (exocuticle, endocuticle and membranous layer) are added proximally in the pre-, and postmoult stages. The calcification takes place in the whole area of carapace at the same time together with the synthesis of organic matrix within the endocuticle. This study demonstrates that the ultrastructure and formation of the cuticle in myodocopans are different from those in podocopans, and that the myodocopan carapaces have achieved a structural diversity for adaptation to different lifestyles.     

Modified pore canals in the cuticle of Gammarus (Crustacea : Amphipoda); A study by scanning and transmission electron microscopy

A novel type of pore canal is described from the cuticle of three species of Gammarus. Each canal passes from the epidermis vertically through the endocuticle and exocuticle, and in the most distal layers of the latter is slightly expanded. Before entering the epicuticle the canal narrows, forming a neck the base of which is encircled by an electron-dense collar. Several tubular structures arise from the collar and pass distally into the reticular innermost regions of the epicuticle. Within the neck and just below its opening at the cuticle surface, a rod-like structure is inserted; this protrudes a short distance from the pore. Each pore canal is connected to many necks; the openings of the latter are aligned in rows over the surface, the openings and rows being about 0.15 and 1.0 μm apart, respectively. Changes in the pore and canal contents are visible and their significance is discussed.     

The structure and modification of integumental tissues in Pagurus bernhardus (L.) (Decapoda: Anomura)

The histological structure of cephalothoracic and abdominal integuments has been studied in the hermit crab Pagurus bernhardus (L.). In the branchial region of the carapace, the integument shows a similar structure as described hitherto in a number of other decapod species; there are a thin epicuticle, an exocuticle, and a relatively thick endocuticle, followed by a layer of columnar epithelium and underlying connective tissue. This pattern is repeated on the inner surface of the carapace fold but with generally thinner cuticular layers. Within the connective tissue there are tegumental glands, haemocytes, and some reserve inclusions. The abdominal integument shows a modified cuticle structure which is probably related to its specific function as an adhesive organ attaching the hermit crab to the inner surface of the gastropod shell. The cuticle is uncalcified and it shows deep wrinkles and grooves. Endocuticle and exocuticle are thick and layered whereas the epicuticle is very thin. Large funnel-shaped ducts with secretions occur frequently in the abdominal integument. The cells that are responsible for these secretions are described. The chemical nature of integumental structures has been studied with histochemical tests.     

The incorporation of precursors into Drosophila larval cuticle

Incorporation of tritiated leucine, tyrosine and glucosamine into the integument of larval Drosophila melanogaster was followed by electron-microscope autoradiography. Tritiated leucine, tyrosine, and glucosamine were incorporated into the endocuticle by apposition, giving rise to a distinct band of label in the endocuticle at a level which depended on the time between labelling and fixation. The labelled amino acids, but not glucosamine, were also detected in the epicuticle and both above and below the distinct labelled band in the endocuticle. The results indicate that the epicuticle grows within the third instar by intussusception of new materials which are transported from the epidermal cells through the endocuticle to the epicuticle. Breakdown of cuticle which was radioactively labelled by feeding larvae tritiated precursors was also followed by autoradiography. The results indicate that the breakdown products from the old cuticle may be reutilized in the synthesis of new cuticle.     

PORE CANALS AND RELATED STRUCTURES IN INSECT CUTICLE

The fine structure and the distribution of an esterase have been studied in the cuticle of Galleria larvae, Tenebrio larvae and pupae, and in the wax-secreting cuticle of the honey bee, and compared with those in the cuticle of the caterpillar of Calpodes. In Galleria and Tenebrio the pore canals are spaces passing through the lamellate endocuticle from the epithelium to the epicuticle. They contain a filament from the cells which may be concerned in their formation. The shape of the pore canal is probably determined by the orientation of the fibres making up the lamellae in the endocuticle and is not a regular helix. The pore canals also contain numerous filaments of another sort which pass on through the epicuticle and are believed to be the origin of the surface wax. They are particularly abundant in the pore canals of the honey bee wax-secreting cuticle and extend into the cell in long pockets surrounded by an envelope of the plasma membrane. The esterase is probably concerned with the final stage of wax synthesis, for its distribution is similar to that of the lipid filaments.     

Histology and histochemistry of the intermoult integument in the ghost crab Ocypoda platytarsis (Milne-Edwards) (Crustacea: Brachyura).

The histological and histochemical aspects of the integument have been described and discussed during the intermoult period of Ocypoda platytarsis. Histological observations revealed that the cuticle comprises of four layers namely epicuticle, exocuticle, endocuticle and membranous layers. Various types of cells in the subepidermal tissue have also been elucidated.     

The Structure and Calcification of the Crustacean Cuticle

The integument of decapod crustaceans consists of an outer epicuticle,an exocuticle, an endocuticle and an inner membranous layerunderlain by the hypodermis. The outer three layers of the cuticleare calcified. The mineral is in the form of calcite crystalsand amorphous calcium carbonate. In the epicuticle, mineralis in the form of spherulitic calcite islands surrounded bythe lipid-protein matrix. In the exo- and endocuticles the calcitecrystal aggregates are interspersed with chitin-protein fiberswhich are organized in lamellae. In some species, the organizationof the mineral mirrors that of the organic fibers, but suchis not the case in certain cuticular regions in the xanthidcrabs. Thus, control of crystal organization is a complex phenomenonunrelated to the gross morphology of the matrix. Since the cuticle is periodically molted to allow for growth,this necessitates a bidirectional movement of calcium into thecuticle during postmolt and out during premolt resorption ofthe cuticle. In two species of crabs studied to date, thesemovements are accomplished by active transport effected by aCa-ATPase and Na/Ca exchange mechanism. The epi- and exocuticular layers of the new cuticle are elaboratedduring premolt but do not calcify until the old cuticle is shed.This phenomenon also occurs in vitro in cuticle devoid of livingtissue and implies an alteration of the nucleating sites ofthe cuticle in the course of the molt.     

Structure of the cuticle of the alpine weta,Hemideina maori (Saussure) (Orthoptera: Stenopelmatidae)

Sclerotized cuticle segments from the thorax, dorsal abdomen, and ventral abdomen of the alpine, weta Hemideina maori (Saussure) (Orthoptera: Stenopelmatidae) were examined by light microscopy and by scanning and transmission electron microscopy. An epicuticle, exocuticle (outer and inner), mesocuticle, endocuticle, and deposition layer are present in transverse sections. The epicuticle is further composed of a cuticulin layer and inner epicuticle, the latter being finely laminated and containing narrow wax canals that terminate below the cuticle surface. Openings to dermal gland ducts are visible on the surface as are large setae and smaller sensory pegs. Frozen fractured cuticle reveals the presence of horizontal ducts or channels that run laterally within the cuticle. The structure of weta cuticle is compared with that of the common house cricket and arthropods in general.     

A proposed solution to a fine-structural puzzle: The organization of gill cuticle in a crayfish (Panulirus)

Crayfish gill cuticle is approximately 2 μm thick and comprises an epicuticle and an endocuticle, which is subdivided into outer and inner layers. Sections demonstrate indistinct lamellae in the outer endocuticle and vertically striated lamellae in the inner endocuticle. Microfibrils cannot be seen in sections. Difficulties in interpretation of the fibrous architecture of the cuticle from thin sections have been overcome by examining tilted series of micrographs of sections and also by making freeze-fracture replicas of the cuticle, which reveal the microfibrils clearly. A model for the endocuticle based on a helicoidal configuration of microfibrillar laminae is proposed and the vertically striated structures seen in sections of the outer layer are accounted for by including regular rows of particles oriented perpendicular to microfibrils. The model is compared with cuticles and coverings reported from other invertebrates.     

Ultrastructure of cuticle deposited inPlodia interpunctella wing discs after variousβ-ecdysone treatments in vitro

Summary Wing discs of the Indian meal moth may be cultured for extended periods in vitro. The discs produced a tanned cuticle after continuous incubation with -ecdysone in medium conditioned with fat body or after a 24-h pulse incubation with -ecdysone in plain medium. We investigated the ultrastructure of the cuticle deposited by such discs. We found that the treatment that produced the most complete cuticle in vitro was the 24-h pulse of hormone. We observed that cuticle formation in vitro was not all-or-none. Depending on culture conditions, discs produced cuticulin only, complete epicuticle, epicuticle plus diffuse endocuticle, epicuticle plus lamellate endocuticle, or even multiple layers of cuticle. The ultrastructural evidence suggests that continuous incubation with -ecdysone in plain medium does not always inhibit cuticle formationper se, but does prevent tanning of the partially formed cuticle.     

Fine structure of the cuticle of the desert scorpion, Hadrurus arizonensis.

The structure of the sclerite and intersegmental cuticle of the opithosoma of the desert scorpion, Hadrurus arizonensis, has been examined by transmission electron microscopy. The sclerite cuticle contains a four-layered epicuticle, a hyaline exocuticle, an inner exocuticle and an endocuticle. The outer part of the hyaline exocuticle and the whole of the inner exocuticle are constructed of helicoidally arranged planes of microfibrils. Within the endocuticle, the overall architecture is not helicoidal as previously assumed, but consists of bundles of microfibrils oriented horizontally and vertically. Microbibrils of the inner exocuticle and the endocutile are seen as simple unstained rods, but those of the hyaline exocuticle are electron dense rods with an unstained central core. The intersegmental cuticle contains a four-layered epicuticle and a procuticle. In detail, its fine structure differs in most respects from that of the sclerite cuticle. Electron microscopy reveals that hyaline exocuticle, previously assumed to be continuous from sclerite to intersegmental membrane, is absent in the latter.     

Ultrastructure of the penetration of the crayfish integument by the fungal parasite, Aphanomyces astaci, Oomycetes

In the crayfish, Astacus astacus, susceptible to the crayfish plague fungus, penetration of the cuticle by the parasite occurred in the soft cuticle. The zoospore lysed the surface lipid layer, tore it away, and formed an infection peg (germ tube) that penetrated through the epicuticle. A septum was formed in the infection peg, and a hypha was formed below the inner epicuticular surface. In the endocuticle, hyphae grew preferrentially parallel to the surface, occassionally perpendicular to it. Growth direction in relation to cuticle architecture is discussed. Subsequently, some hyphae started to penetrate out through the epicuticle. This process was preceded by the swelling of the hyphal tip touching the inner side of the epicuticle. The hypha penetrating out through the epicuticle was much thicker than the infection peg. Histolytic activity, combined with mechanical penetration, seems to be evident in all stages and levels except in the outward penetration of the epicuticular lipid surface layer, where only mechanical rupture could be seen. Differences in the protoplasmic ultrastructure were found between the spore and the penetrant hyphae. Penetration of the cuticle of a resistant crayfish was essentially identical to that in susceptible ones. However, inward penetration of intact epicuticle was too scarce to allow for ultrastructural studies.     

Histochemistry of the cuticle of the crab Menippe rumphii (Fabricius) (Crustacea: Brachyura) in relation to moulting

Histological and histochemical methods have been employed to study the formation and growth of the exoskeleton in relation to the moulting cycle of the crab Menippe rumphii (Fabricius). In the premoult condition the epidermal cells secrete a two-layered cuticle. Later these layers are widened by the secretions coming from the reserve cells, tegumental glands, and the Leydig cells. The fully formed cuticle of the intermoult crab is divisible into four layers, epicuticle, exocuticle, mesocuticle, and endocuticle.Histochemical observations on different cells have revealed that the tegumental glands secrete both neutral and acid mucopolysaccharides. The reserve cells are positive to PAS, BPB, Sudan Black B and Alizarin Red S techniques indicating the presence of carbohydrates, proteins, lipids, and mineral calcium. The Leydig cells are loaded with enzymes, including alkaline phosphatase, acid phosphatase, lipase, and phenoloxidase. Other histochemical tests have been employed to investigate the formation of different layers of the cuticle.     

Internal anatomy of Hypochthonius rufulus (acari: Oribatida)

The internal anatomy of juveniles and adults of Hypochthonius rufulus selected as a model species representing the lower Oribatida was investigated histologically and compared with the published characteristics of higher oribatid internal anatomy. In this species, the cuticle is weak and flexible, consisting of epicuticle and endocuticle on the body, but including an exocuticle between the epicuticle and endocuticle of the legs. Walls of the mesenteron in the digestive tract are of uniform thickness and structure without any regional thickening, and there are no proventricular glands. The hindgut is apparently divided into five parts: colon 1 and 2, rectum 1 and 2, and anal atrium; food bolus exhibits a multilamellar structure in this section. The glandular system is less diversified than in some other oribatids. Tracheae are apparently lacking. Females possess only two relatively large eggs, filling one-half of opistosoma, and they lack ovipositors. Eggs are present in females during the whole year. Gonad buds appear first in the protonymph stage. Only one male was found among 146 adults studied. No male external organ (aedeagus or penis) is present.     

Cuticular adaptations in two parasitic copepods in relation to their modes of life

The structure, histochemistry, and possible functional properties of the cuticle in two parasitic copepods Pennella elegans Gnanamuthu and Caligus savala Gnanamuthu have been studied: the former is partially embedded in the host while the latter is an ectoparasite capable of free swimming.In Pennella elegans the cuticle of the embedded anterior region of the body is soft, colourless, and lacks an outer epicuticle while that of the posterior exposed part is pigmented and hard. Conspicuous in the cuticle of the ventral region of the head are pore canals which, though not chitinized, are functional even in the intermoult stage: these canals may be involved in the transport of nutrient materials from the host. The horns, which serve to fix the parasite firmly in the host tissues, are covered by cuticle in which the epicuticle and outer layers of the procuticle are hardened by formation of disulphide linkages. The cuticle of the neck region is not hardened and the procuticle in this region shows transverse regions of dense and light zones probably related to the coiling of the neck during penetration. The epicuticle is two layered in the cuticle of the exposed posterior region, the inner epicuticle and outer region of the procuticle being partially hardened by phenolic tanning so confer rigidity and resistance. The cuticle of the plumes is soft and devoid of an outer lipid epicuticle and so possibly adapted for a respiratory function.In Caligus savala, the epicuticle is two layered, and the procuticle has pigmented, calcified, and uncalcified layers. The cuticle is hardened by phenolic tanning as well as by calcification thus recalling the cuticular organization of decapod crustaceans.     

Fine structure of the cuticle of the black widow spider with reference to surface lipids

The surface and transverse sections of the cephalothorax, abdomen, and walking leg cuticle of the black widow spider, Latrodectus hesperus, were examined by scanning and transmission electron microscopy. Cuticle that was untreated prior to normal EM preparative procedures was compared with cuticle subjected to lipid solvents and/or concentrated alkali. The surface of untreated dorsal cephalothorax cuticle contained droplets and a lipid film that obscured fine surface detail. Immersing the cuticle in chloroform: methanol removed the droplets and lipid film, exposing previously covered openings to dermal gland ducts. An epicuticle, exocuticle, and endocuticle were present in all transverse sections of cuticle as was a complex system of pore and wax canals that connected the epidermis with the cuticle surface. The epicuticle of the walking leg was composed of three sublayers: outer membrane, outer epicuticle, and the dense homogeneous layer. A cuticulin layer was not observed. Lipid solvents did not significantly alter the morphology of any of these layers or the contents of the wax/pore canals.