Spermiogenesis in Phyllobothrium lactuca Beneden, 1850 begins with the formation of a differentiation zone bordered by cortical microtubules and containing a nucleus and two ccntrioles separated by an intercentriolar body and disposed one in the prolongation of the other. Later, formation of flagellar buds, striated roots and a median cytoplasmic extension takes place. Each centriole gives rise to a flagellimi that rotates and fuses with the median cytoplasmic extension. At this stage, arched membranes appear at the front of the differentiation zone. The nucleus elongates, becomes filiform and migrates between the striated roots into the spermatid. After the migration of the nucleus, the old spermatid separates from the residual cytoplasm by strangulation of the ring of arched membranes. Absence of striated roots, right at the beginning of spermiogenesis has never been described before in the Tctraphyllidea. Likewise, centrioles made up of doublets of microtubules and spermatids with two axonemes have never been reported before during spermiogenesis of a Phyllobothriidae. In this work we show, for the first time, the existence in cestodes of thick-walled microtubulcs surrounded by a layer of electron-dense material. In addition, we describe, for the first time, the existence of an accumulation of electron-dense granules around striated roots and an hour-glass-shaped constriction at the anterior extremity of a median cytoplasmic extension in a platyhelminth.
In the apical glandular region of the adult Proteocephalus torulosus (Batsch, 1786), two types of eccrine gland cells are present. The first type of unicellular gland produces large electron-dense granules of various sizes. The second type contains small electron-dense granules. Most cells form glands with large granules; glands with small granules are infrequent. The secretion of both types of gland cells is concentrated in the apical parts of the cyton and in the ducts opening to the exterior. On the scolex of P. torulosus, there are regional structural differences of the microthrix border. The apical glandular region bears filamentous microtriches only. On the remaining frontal part, surrounding the glandular region, there are blade-like and filamentous microtriches. The lateral parts of the scolex and suckers bear blade-like microtriches. Possible functions of both types of gland cells and different parts of the scolex microthrix border are discussed. The unique structure of the frontal part of the scolex of P. torulosus and its differences from Proteocephalus macrocephalus, P. longicollis and P. percae correlate well with the putative basal phylogenetic position of P. torulosus among European species of Proteocephalus.
The ultrastructure of the scolex tegument, bothridial pits (“ciliated pits) and rhyncheal system of Otobothrium mugilis Hiscock, 1954 is described from plerocerci collected from the teleosts Arius graeffei Kncr ct Steindachner and Mugil cephalus Linnaeus. Scanning electron microscopy revealed that filamentous microtriches with shortened caps are abundant across the entire surface of the tegument. Palmate microtriches are dominant on the bothridia and their margins. The surfaces of bothridial pits were covered with large bifid microtrichcs. The bothridial pits arc strongly muscularised invaginations of the tegument. Nervous tissues were not observed within the pits and it is probable that these structures function as accessory attachment structures. The wall of each tentacle sheath consists of one to three bands of fibrils, lined internally by a thin cytoplasmic layer. The tentacular walls are cellular, containing myofilaments. The fibrils of the tentacular walls are arranged into discrete blocks of parallel fibrils and appear to be intracellular. Tentacular walls are lined externally by a modified membrane with an external glycocalyx. Tentacular hooks arc solid, bound externally by a membrane. The body of the hook contains numerous longitudinal canaliculi and an elcctron-opaquc medulla lies at the centre of the hook.
The surface structures and gland cells of the posterior rosette organ of Gyrocotyle urna Grube et Wagener, 1852, a member of the group presumed to be the most basal of the tapeworms (Cestoda: Gyrocotylidea), was studied by scanning electron and transmission electron microscopy. Surface structures on the outer (oriented away from the intestinal wall) and inner (in contact with the intestinal wall) rosette surfaces differ from each other and represent a transitional form between microvilli and microtriches typical of tapeworms (Eucestoda). The inner surface of the rosette possesses numerous glands. On the basis of the size and electron-density of their secretory granules, three types of unicellular gland cells can be distinguished. The least common type (Type I) is characterized by the production of small, round, electron-dense granules of about 0.3 µm in diameter, whereas another type of secretion (Type II) is formed from homogenous, moderately electron-dense, spheroidal granules of about 0.7 µm in diameter. The most common type of glands (Type III) is recognized by a secretion comprising large, elongate, electron-dense granules of about 1 µm long and 0.5 µm broad. The secretory granules of the three types of the glands are liberated by an eccrine mechanism and the gland ducts open via small pores on the inner rosette surface. The complex of secretory glands of the posterior rosette of G. urna is similar to those in the anterior attachment glands of monogeneans (as opposed to the types of glands present in other helminth groups). However, the tegumental surface structures of Gyrocotyle are supporting evidence for the relationship between the Gyrocotylidea and Eucestoda.
The ultrastructure of three types of unicellular scolex gland cells in adult cestode Bothriocephalus claviceps (Goeze, 1782) is described. The first type - apocrine gland cells transport their secretion (small rounded electron dense granules) via thin ducts into the tegument where it accumulates as projections on the body surface. The second type - eccrine gland cells press out their secretion (large oval electron dense granules) through ducts which open to the exterior surface of the tegument. The third type - microapocrine gland cells transport their secretion (large rounded electron dense granules) through thin cytoplasmic processes into the distal cytoplasm of the tegument. The secretory discharge occurs by means of évaginations of the outer tegumental plasmalemma and their subsequent detachment. The possible functions of the scolex gland cells are discussed.
Terminology for microtriches, the surface features both unique to and ubiquitous among cestodes, is standardised based on discussions that occurred at the International Workshops on Cestode Systematics in Storrs, Connecticut, USA in 2002, in České Budějovice, Czech Republic in 2005 and in Smolenice, Slovakia in 2008. The following terms were endorsed for the components of individual microtriches: The distal, electron-dense portion is the cap, the proximal more electron-lucent region is the base. These two elements are separated from one another by the baseplate. The base is composed of, among other elements, microfilaments. The cap is composed of cap tubules. The electron-lucent central portion of the base is referred to as the core. The core may be surrounded by an electron-dense tunic. The entire microthrix is bounded by a plasma membrane, the external layer of which is referred to as the glycocalyx. Two distinct sizes of microtriches are recognised: those <= 200 nm in basal width, termed filitriches, and those >200 nm in basal width, termed spinitriches. Filitriches are considered to occur in three lengths: papilliform (<= 2 times as long as wide), acicular (2-6 times as long as wide), and capilliform (>6 times as long as wide). In instances in which filitriches appear to be doubled at their base, the modifier duplicated is used. Spinitriches are much more variable in form. At present a total of 25 spinithrix shapes are recognised. These consist of 13 in which the width greatly exceeds the thickness (i.e., bifid, bifurcate, cordate, gladiate, hamulate, lanceolate, lineate, lingulate, palmate, pectinate, spathulate, trifid, and trifurcate), and 12 in which width and thickness are approximately equal (i.e., chelate, clavate, columnar, coniform, costate, cyrillionate, hastate, rostrate, scolopate, stellate, trullate, and uncinate). Spiniform microtriches can bear marginal (serrate) and/or dorsoventral (gongylate) elaborations; they can also bear apical features (aristate). The latter two modifiers should be used only if the features are present. The terminology to describe the overall form of a spinithrix should be used in the following order: tip, margins, shape. Each type of microthrix variation is defined and illustrated with one or more scanning electron micrographs. An indication of the taxa in which each of the microthrix forms is found is also provided.
The vitellogenesis of Paraechinophallus japonicus (Yamaguti, 1934), the first pseudophyllidean tapeworm of the family Echinophallidae studied using transmission electron microscope, is described on the basis of ultrastructural observations of specimens from the benthopelagic fish Psenopsis anomala (Temminck et Schlegel, 1844) (Perciformes: Centrolophidae). The process of vitellogenesis in P. japonicus follows the same general pattern observed in other tapeworms. Five stages of vitellocyte development have been distinguished. The first stage corresponds to immature cells containing ribosomes and mitochondria. The second stage of development is characterized by the appearance of granular endoplasmic reticulum and Golgi complexes, formation of shell globules and lipid droplets at the periphery of the cell cytoplasm. Vitellocyte of the third stage presents accumulation of shell globules and lipid droplets. During the fourth stage, shell globule clusters are formed, and lipid droplets and rosettes of α-glycogen are accumulated. Mature vitelline cells are characterized by a great number of lipid droplets with glycogen in the centre of the cytoplasm, whereas shell globule clusters are situated more peripherally. The interstitial tissue of vitelline follicles of P. japonicus is syncytial with long cytoplasmic projections extending between vitelline cells. The presence of a large amount of lipid droplets in the vitelline cytoplasm within the eggs of P. japonicus may be related to egg accumulation in the uterine sac.