Abstract

BackgroundIn Europe, the tapeworm Dibothriocephalus latus (syn. Diphyllobothrium latum) is a well-known etiological agent of human diphyllobothriosis, which spreads by the consumption of raw fish flesh infected by plerocercoids (tapeworm’s larval stage). However, the process of parasite establishment in both intermediate and definitive hosts is poorly understood. This study was targeted mainly on the scolex (anterior part) of the plerocercoid of this species, which facilitates penetration of the parasite in intermediate paratenic fish hosts, and subsequently its attachment to the intestine of the definitive host.MethodsPlerocercoids were isolated from the musculature of European perch (Perca fluviatilis) caught in Italian alpine lakes. Parasites were examined using confocal microscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Immunofluorescence tagging was held on whole mount larvae.ResultsThe organisation of the central and peripheral nervous system was captured in D. latus plerocercoids, including the ultrastructure of the nerve cells possessing large dense neurosecretory granules. Two types of nerve fibres run from the body surface toward the nerve plexus located in the parenchyma on each side of bothria. One type of these fibres was found to be serotoninergic and possessed large subtegumental nerve cell bodies. A well-developed gland apparatus, found throughout the plerocercoid parenchyma, produced heterogeneous granules with lucent core packed in a dense layer. Three different types of microtriches occurred on the scolex and body surface of plerocercoids of D. latus: (i) uncinate spinitriches; (ii) coniform spinitriches; and (iii) capilliform filitriches. Non-ciliated sensory receptors were observed between the distal cytoplasm of the tegument and the underlying musculature.ConclusionsConfocal laser scanning microscopy and electron microscopy (SEM and TEM) showed the detailed microanatomy of the nervous system in the scolex of plerocercoids, and also several differences in the larval stages compared with adult D. latus. These features, i.e. well-developed glandular system and massive hook-shaped uncinate spinitriches, are thus probably required for plerocercoids inhabiting fish hosts and also for their post-infection attachment in the human intestine.

Highlights

  • These two species differ in the morphology and life-cycle strategy of their larval stages, and in preferences for the second intermediate and definitive hosts [4]

  • Kuperman & Davydov [14] stated that the glandular system of D. latus is much more developed in comparison with its congeners; this may coincide with the higher invasive potential of D. latus than that of D. dendriticus and D. ditremus (Creplin, 1925), as tested on paratenic hosts [15]

  • Immunocytochemistry In the conventionally processed D. latus plerocercoids, the compartments of the central nervous system (CNS) were labelled by an antibody triad, i.e. anti-5-HT, antiFMRF amide and anti-synapsin, and the cell tubular system was visualised by the anti-β tubulin antibody

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Summary

Introduction

In Europe, the tapeworm Dibothriocephalus latus (syn. Diphyllobothrium latum) is a well-known etiological agent of human diphyllobothriosis, which spreads by the consumption of raw fish flesh infected by plerocercoids (tapeworm’s larval stage). Most ultrastructural and immunochemistry/immunofluorescense-based studies of diphyllobothriidean plerocercoids have dealt with the congeneric species, Dibothriocephalus dendriticus (Nitzsch, 1824) [9,10,11,12,13], while few have investigated D. latus [14]. These two species differ in the morphology and life-cycle strategy of their larval stages (the former remain in the body cavity, while the latter migrate to the musculature), and in preferences for the second intermediate and definitive hosts [4]. Kuperman & Davydov [14] stated that the glandular system of D. latus is much more developed in comparison with its congeners; this may coincide with the higher invasive potential of D. latus than that of D. dendriticus and D. ditremus (Creplin, 1925), as tested on paratenic hosts [15]

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