Abstract
The invasive larvae (cercariae) of schistosomes penetrate the skin of their definitive hosts. During the invasion, they undergo dramatic ultrastructural and physiological transitions. These changes result in the development of the subsequent stage, schistosomulum, which migrates through host tissues in close contact with host’s immune system. One of the striking changes in the transforming cercariae is the shedding of their thick tegumental glycocalyx, which represents an immunoattractive structure; therefore its removal helps cercariae to avoid immune attack. A set of commercial fluorescently labeled lectin probes, their saccharide inhibitors and monoclonal antibodies against the trisaccharide Lewis-X antigen (LeX, CD15) were used to characterize changes in the surface saccharide composition of the neuropathogenic avian schistosome Trichobilharzia regenti during the transformation of cercariae to schistosomula, both in vitro and in vivo. The effect of various lectins on glycocalyx shedding was evaluated microscopically. The involvement of peptidases and their inhibitors on the shedding of glycocalyx was investigated using T. regenti recombinant cathepsin B2 and a set of peptidase inhibitors. The surface glycocalyx of T. regenti cercariae was rich in fucose and mannose/glucose residues. After the transformation of cercariae in vitro or in vivo within their specific duck host, reduction and vanishing of these epitopes was observed, and galactose/N-acetylgalactosamine emerged. The presence of LeX was not observed on the cercariae, but the antigen was gradually expressed from the anterior part of the body in the developing schistosomula. Some lectins which bind to the cercarial surface also induced secretion from the acetabular penetration glands. Seven lectins induced the shedding of glycocalyx by cercariae, among which five bound strongly to cercarial surface; the effect could be blocked by saccharide inhibitors. Mannose-binding protein, part of the lectin pathway of the complement system, also bound to cercariae and schistosomula, but had little effect on glycocalyx shedding. Our study did not confirm the involvement of proteolysis in glycocalyx shedding.
Highlights
Trichobilharzia regenti (Trematoda, Schistosomatidae) is a neuropathogenic avian schistosome that migrates through the CNS to nasal areas of anatid birds
The transformation of cercaria to schistosomulum is accompanied by extensive changes, characterized by a loss of multifucosylated GalNAcβ1-4GlcNAc (LDN) O-glycoproteins, which are replaced by LDN-rich glycosphingolipids [13,14,15,16]
Our study focused on qualitative changes in surface glycosylation of T. regenti during the transformation of cercariae to schistosomula both in vivo and in vitro, and on microscopic observation of the process of glycocalyx shedding by cercariae either in the presence of linoleic acid, or during the action of exogenous lectins, including mannose-binding protein known to activate the lectin pathway of the complement system
Summary
Trichobilharzia regenti (Trematoda, Schistosomatidae) is a neuropathogenic avian schistosome that migrates through the CNS to nasal areas of anatid birds. Cercariae emerging from the snail intermediate host actively penetrate the skin of their definitive bird hosts or accidental (dead-end) mammalian hosts, including humans, and transform to schistosomula [4]. This process is accompanied by a detachment of the cercarial tail and emptying of the penetration glands. Cercarial bodies generally undergo extensive ultrastructural rebuilding that is accompanied by changes in biochemical processes and molecular (antigenic) composition of the tegumental glycocalyx. Transforming larvae form a double outer tegumental membrane with protective function, and shed the highly immunogenic glycocalyx which had protected them against the aquatic environment [5,6]. The transformation of cercaria to schistosomulum is accompanied by extensive changes, characterized by a loss of multifucosylated GalNAcβ1-4GlcNAc (LDN) O-glycoproteins, which are replaced by LDN-rich glycosphingolipids [13,14,15,16]
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