The role of microtubules in the secretory processes in the tegument of adult trematode Fasciola hepatica L. is studied by estimating the effects of colchicine, a substance known to disrupt microtubules, on the number of T2 vesicles. Tissue slices of Ihe worm are incubated in Hedon-Fleig medium with or without 5 x 10'4M colchicine. The dynamics of the colchicine-provoked secretory block is examined by morphometry on samples processed for electron microscopy. T2 vesicles are estimated as a total number or separately within three levels (apical, sub-apical and central) of the distal tegument. The secretory block is demonstrated as reduction in the total number of T2 vesicles. The separate counting within three levels of the distal tegument demonstrates in control samples a trend of sub-apical condensation of T2 vesicles. This pattern of T2 distribution remains unchanged in colchicine-treated samples in spite of the reduction of the mean T2 counts within each of the levels examined. The data illustrate the role of microtubules in both the tegumental transport of secretory vesicles and the stratification of the organelles within the tegument.
The tegument ultrastructure of the cestode Triaenophorus nodulosus has been studied in the stages of oncosphere, procercoid, plerocercoid and adult. The syncytium of primary tegument has glandular origin and is located in the peripheral areas of the oncosphere. The primary tegument degenerates at the initial stages of the procercoid development and is replaced with secondary tegument persisting throughout all following stages of the worm’s development. Two ways of microthrix formation on the body surface of procercoid were discovered. The formation of the cyst consisting of fibrillar material around the plerocercoid was observed. It fills spaces between numerous finger-like évaginations of plerocercoid’s tegument. The structural differentiation of tegument and microtriches was demonstrated on the scolex and all parts of strabila of T. nodulosus.
The ultrastructure and histochemistry of the tegument and penetration glands of adult Amphilina foliacea from the body cavity and the tissues of the internal organs of Acipenser ruthenus and A. stellatus were studied. New data on the localization in the tissue, development and in encapsulation of the adult A. foliacea mostly in the liver of A. ruthenus were obtained. The well developed penetration glands are necessary for penetration into the tissue and for migration of A. foliacea into the body cavity of the hosts. The tegument of the adult A. foliacea is a syncytium with cytons deeply embedded into the parenchyma. The secretory activity of the tegument of worms has a protective function against the immune system of the host. Our results give further information about the phylogeny of Amphilinidea and confirm the view of the close phylogenetic relationship of Amphilinidea and Cestoidea.
The ultrastructure and chemical composition of the proboscis hooks and surrounding tegument of Acanthocephalus lucii (Müller, 1776), a parasite of European perch, Perca fluviatilis Linnaeus, were examined using scanning (SEM) and transmission (TEM) electron microscopy and X-ray microanalysis (EDXA). The blade of middle hooks consists of three layers: an outer homogeneous layer, an inner heterogeneous layer and a central core. TEM observation revealed the presence of hollow tubes, which spaced the central core; fibrous inner hook layer surrounded by an electron-dense margin and the basal tegumental layer filled with electron-dense bodies and outer layer. We found for the first time that the so-called ''epidermal covering'' surrounding of the exposed hook blade (outer hook layer) is a modified striped portion of the tegumental layer and there are no special contact sites between these two morphologically different structures, i.e. striped layer of the syncytial tegument and following proper outer hook layer, which is a homogeneous, moderately electron-dense layer of ~0.3 µm in thickness. The hook root is embedded into subtegumental fibrous layer. X-ray microanalysis of both the surface and internal parts of A. lucii hooks demonstrated the presence of calcium, magnesium, phosphorus and sulphur. The highest concentration of sulphur was recorded at the tip of hooks, whereas the middle part of the hooks was most rich in calcium, phosphorus and magnesium. The proximal part of the hooks contained lower concentrations of sulphur, calcium and phosphorus. In the proboscis tegument, only two elements, calcium and silicon, were found. The differences observed in the chemical composition of the hook ''epidermal covering'' and the proboscis tegument support our ultrastructural findings that the hook tegumental covering is a modified structure compared with that of the general proboscis tegument.
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.