Abstract

Both the oncospheral tegument and the hook region membrane (HRM) of Echinococcus multilocularis hexacanths originate from a syncytial binucleate complex that appears in the early stage of morphogenesis and organogenesis of the hexacanth larva. The primordium of this binucleate complex forms a binucleate syncytial cap or “calotte” situated beneath the inner envelope at one pole of the developing embryo. During oncospheral differentiation, the binucleate perikaryon of the syncytial cap is sunk progressively deeper into the central part of the embryo, but remains always connected with the distal cytoplasm by a tendrillar cytoplasmic connection or bridge. Following migration or sinking of the binucleate perikaryon, numerous cytoplasmic vesicles appear in the distal cytoplasm. These vesicles fuse progressively together and form a single large cavity or lacuna. The walls of this cavity are becoming at this point the walls of two delaminated layers: (1) the distal anucleated cytoplasmic layer is transformed into the oncospheral tegument and (2) the proximal thin cytoplasmic layer is transformed into the “hook region membrane”. This delamination of the initially compact layer of distal cytoplasm into two layers seems to be closely associated with differentiation of oncospheral hooks, the elongating blades of which protrude progressively into a newly formed cavity. The pressure of hook blades on the hook region membrane appears to facilitate its further separation from the basal layer of distal cytoplasm which is transformed into the peripheral layer of oncospheral tegument. In the mature oncosphere, the surface of this peripheral layer forms a regular brush border of cytoplasmic processes or microvilli and represents the true body covering of the hexacanth. The very thin cytoplasmic connection between the peripheral layer of tegument and binucleate perikaryon appears only very seldom in the ultrathin sections as a narrow cytoplasmic strand and has a plasma membrane that is reinforced by a single row of cortical microtubules. The HRM covers only one pole of the oncosphere and is attached to the oncosphere surface. The HRM is clearly visible in the mature oncosphere and is draped over the hook blades, the sharp points of which are protected by moderately electron-dense caps. Comparison of the above morphology with that of TEM study of the tegument of adult cestodes shows a great similarity as well as homology in the body covering of both larval and adult cestodes.

Highlights

  • The ultrastructure of the oncospheral tegument and hook region membrane cannot be understood without an account of their origin and differentiation (Lee 1966; Lumsden et al 1974; Threadgold 1984)

  • In Echinococcus multilocularis, both the oncospheral tegument (OT) and associated hook region membrane (HRM) covering only one pole of the hexacanth, originates from a syncytial binucleate complex (PBC), which appears at the early stage of morphogenesis and organogenesis (Figs. 1a, 2 and 3a)

  • The binucleate cells of E. multilocularis embryos resemble such cells described previously in embryos of other cestode species; they have been identified as the embryonic sunken tegumental cells

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Summary

Introduction

The ultrastructure of the oncospheral tegument and hook region membrane cannot be understood without an account of their origin and differentiation (Lee 1966; Lumsden et al 1974; Threadgold 1984). Detailed TEM studies on Parasitol Res (2018) 117:783–791 oncospheres are very rare because of numerous technical difficulties. They have been conducted on four cestode species: Hymenolepis diminuta by Rybicka (1973), Catenotania pusilla by Świderski (1968, 1972) and two species of dilepidid cestodes, Anomotaenia constricta and Paricterotaenia porosa by Gabrion (1981). The purpose of the present study is a reexamination of the earlier study and re-description of the origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane of E. multilocularis with application of new, much improved modern methods of TEM involving cryofixation and TEM cytochemistry. Samples were rinsed in a 0.15 M glycine in a 0.1 M sodium cacodylate buffer at pH 7.4, cryoprotected by crescent concentrations (10, 20 and 30%) of glycerol in the same buffer, and cryofixed in liquid propane

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