Light and transmission electron microscopy of the haptoral sclerites of the monogenean gill parasite Macrogyrodactylus clarii.

The present study represents the first detailed description of the haptoral sclerites of Macrogyrodactylus clarii Gussev 1961. Light microscopy reveals outgrowths of the hamuli roots; two lateral spine-like extensions of the hood-like accessory sclerites; a ridged, fan-shaped distal end of an accessory sclerite; and two thread-like accessory sclerites with biforked ends associated with the pointed hooked region of each hamulus. Transmission electron microscopy (TEM) reveals the presence of parallel tubules in the root of the hamuli and structural differences along the length of the hamulus including the root, shaft, and pointed hooked region. The root consists of two layers, the shaft four layers and pointed hooked region only one layer with dense outer serrations. Characteristic features of the hamulus root are the presence of longitudinally orientated parallel tubules in its central core and parallel electron-dense ridges in the outer layer of its middle region; features not observed in either the shaft or the pointed hooked region. Each hamulus blade of M. clarii is associated with haptoral gland cells producing electron-dense secretory bodies. The 16 marginal hooklets each consist of a blade (sickle) articulating with a handle at the guard region and a domus. TEM revealed structural differences between the handle, the blade at the articulation region, and the distal hooked region. The domus, a filamentous thread-like sclerite at the light microscope level, consists of two electron-dense, fibrous thickenings connected to each other by a cytoplasmic process. Each marginal hooklet is associated with a small cavity and a large reservoir of homogeneous particles and secretory bodies. The possible functions of these structures are discussed in relation to equivalent features in other monogeneans.

Ultrastructure of the anterior adhesive apparatus of the gill parasite Macrogyrodactylus clarii and skin parasite M. congolensis (Monogenea; Gyrodactylidae) from the catfish Clarias gariepinus.

Transmission electron microscopy (TEM) was used for the first time to study the anterior adhesive apparatus of the monogeneans Macrogyrodactylus clarii Gussev, 1961 and M. congolensis (Prudhoe, 1957) Yamaguti, 1963 inhabiting gills and skin respectively of the same catfish Clarias gariepinus. Despite the different microhabitats occupied by these parasites, the present study revealed that they have a similar anterior adhesive system. In both parasites, the anterior adhesive apparatus consists of three types of gland cells: G1 cells that produce rod-shaped bodies (S1), G2 cells manufacture irregularly shaped bodies (S2) and G3 cells form mucoid-like secretions (S3). In the cytoplasm of G1 cells, a single layer of microtubules encloses each developing rod-shaped body. A unique feature of S1 secretory bodies is that some fully developed S1 bodies are attached to each other, forming large condensed globules in the cytoplasm of G1 gland cells and terminal portion of the G1 ducts, but none were detected in the adhesive sacs outside the ducts. In the adhesive sacs, G1 ducts open with multiple apertures whereas each of the G2 and G3 ducts have a single opening. The adhesive sacs are lined with two types of tegument (st1 and st2). A third tegument type (st3) connects the st2 tegument with the general body tegument. Only st1 has microvilli. Each adhesive sac is provided with a spike-like sensillum and single uniciliated sense organ. The possible functions of microvilli in increasing the surface area and assistance in spreading and mixing of the adhesive secretion, and the role of sense organs associated with the adhesive sacs are discussed.

Histochemical demonstration of five enzymes' activities in Macrogyrodactylus clarii (Monogenea: Gyrodactylidae) from the catfish Clarias gariepinus.

Histochemical techniques were applied to whole mounts, to study the distribution of the enzymes alkaline phosphatase, acid phosphatase, adenosine triphosphatase, 5'-nucleotidase and glucose-6-phosphatase in the organs and tissues of a viviparous monogenean, Macrogyrodactylus clarii Gussev, 1961, from the gills of the North African catfish Clarias gariepinus (Burchell) in Egypt. The following organs and tissues were studied: head region, anterior adhesive glands, mouth region, pharynx, intestine, testis, vesicula seminalis, male accessory gland, male accessory reservoir, copulatory organ, receptaculum seminis, egg-cell forming region, embryonic cells, excretory system, nerve cells, haptor, muscle fibres and subtegumental cell bodies (cytons). The enzymes showed marked differences in their activities among the studied organs and tissues. Alkaline phosphatase and acid phosphatase activities were detected in many organs and tissues, while the activities of adenosine triphosphatase, 5'-nucleotidase and glucose-6-phosphatase were restricted to a few organs. Although no positive reaction for any enzyme was observed in the anterior adhesive gland cells, a positive reaction for acid phosphatase was detected in the anterior adhesive areas. All enzymes showed marked activity in the digestive and excretory systems. The distribution of the enzymes in the tissues and organs of M clarii is compared with those of other monogeneans, including other gyrodactylids parasitizing the same host fish. Some possible functions of the enzymes are discussed.

Surface features of the monogenean gill parasites Pseudodactylogyrus anguillae and Pseudodactylogyrus bini from the European eel Anguilla anguilla in Egypt.

In the present study, scanning electron microscopy is used to demonstrate the surface features of Pseudodactylogyrus anguillae Yin and Sproston (1948) Gussev, 1965 and Pseudodactylogyrus bini Kikuchi (1929) Gussev, 1965 from the European eel Anguilla anguilla. Specimens of the eel A. anguilla were collected from the River Nile, near Mansoura, Dakahlia Province, Egypt. Morphologically, P. anguillae could be distinguished from P. bini based on the total length, the shape and size of the haptor, and the constriction between the haptor and body proper. The general body tegument and the haptoral tegument of both species are microvillous. Possible functions of the microvilli associated with the tegument covering the anterior adhesive areas are discussed. The region of the body proper just anterior to the haptor of P. anguillae, appears to be highly folded and provided with many projections forming scale-like structures. Many surface ciliary sensilla presumed to be sensory structures are found on the tegument of the anterior adhesive area of P. anguillae. Secretory bodies and mucus-like substances are recorded on the tegument covering the anterior adhesive areas of P. anguillae and the haptor of P. bini. The possible role of these secretions in the attachment of the anterior adhesive areas and the posterior attachment haptor to the host tissues are also discussed.

Scanning electron microscope observations on the monogenean parasite Paraquadriacanthus nasalis from the nasal cavities of the freshwater fish Clarias gariepinus in Egypt with a note on some surface features of its microhabitat.

Surface features of the monogenean Paraquadriacanthus nasalis Ergens, 1988 (quoted by Kritsky, 1990) inhabiting the nasal cavities of the freshwater fish Clarias gariepinus were studied for the first time using scanning electron microscopy. The anterior adhesive areas possess two slit-like openings. Many small openings were detected on the tegument covering the anterior-most region of the head. Some considerably large openings were also found in the median region between the two slit-like openings of the adhesive sacs. A transverse slit-like mouth opening with two lip-like structures was detected on the ventral surface of the body. Three types of presumed sensory structures were found associated with the tegument of the anterior adhesive area and anterior region of the body. These are surface ciliary sensilla, dome-shaped structures, and many spherical structures. The possible functions of these presumed sensory structures were discussed. The tegument covering the anterior adhesive area lacks microvilli, while the tegument covering the haptor is associated with microvilli. The haptoral sclerites were found in two different positions. Some surface features of the nasal cavities of C. gariepinus (microhabitat of P. nasalis) were also studied using scanning electron microscopy. Many lamellae-like and spine-like structures were recognized. The epithelium lining in some regions of the nasal cavities has small and large openings and covered with mucus. The possible roles of some haptoral sclerites in the attachment of the parasite to the host tissues were discussed.