Characterization of surface antigens of Trichinella spiralis infective larvae

Infective larvae of Trichinella spiralis were surface‐labelled with radioactive iodine, and the products were characterized biochemically and immunochemically. The labelled material was restricted to two basic subunits: a lentil lectin‐adherent glycoprotein (GP), mol. wt 47K, and a lentil lectin‐non‐adherent protein fraction (P), mol. wt 55K. Both of these form homologous dimers through as yet unspecified covalent bonds to yield GP90 and P105. The GP is further polymerized into higher molecular weight forms by disulphide bond‐dependent associations, suggesting a highly cross‐linked arrangement in the cuticle. To what extent this structure contributes to the overall organization of the cuticle remains to be established. The two labelled surface molecules are immunogenic in the infected host, and do not react with a panel of sera taken from animals chronically infected with other nematode species. The approach therefore offers immediate possibilities for immunodiagnosis in nematode infections, and for a comparative immunochemical study of the surface cuticle of different stages of the same and different nematode species and for studies of the function of the nematode cuticle.

[1]  R. Parkhouse,et al.  Immune response to stage-specific surface antigens of the parasitic nematode Trichinella spiralis , 1981, The Journal of experimental medicine.

[2]  R. Parkhouse,et al.  Changing proteins on the surface of a parasitic nematode , 1980, Nature.

[3]  R. Maizels,et al.  The surface of nematodes and the immune response of the host. , 1980 .

[4]  T. Potter,et al.  Murine lymphocyte surface antigens. , 1979, Advances in Immunology.

[5]  R A Laskey,et al.  Enhanced autoradiographic detection of 32P and 125I using intensifying screens and hypersensitized film , 1977, FEBS letters.

[6]  R. Lerner,et al.  Radioiodination of proteins in single polyacrylamide gel slices. Tryptic peptide analysis of all the major members of complex multicomponent systems using microgram quantities of total protein. , 1977, The Journal of biological chemistry.

[7]  D. Despommier,et al.  The stichosome and its secretion granules in the mature muscle larva of Trichinella spiralis. , 1976, The Journal of parasitology.

[8]  P. O’Farrell High resolution two-dimensional electrophoresis of proteins. , 1975, The Journal of biological chemistry.

[9]  D. McLaren The anterior glands of adult Necator americanus (Nematoda: Strongyloidea). I. Ultrastructural studies. , 1974, International journal for parasitology.

[10]  P. Ambroise‐Thomas Immunological diagnosis of human filariases: present possibilities, difficulties and limitations. , 1974, Acta tropica.

[11]  J. Marchalonis,et al.  Enzymic iodination. A probe for accessible surface proteins of normal and neoplastic lymphocytes. , 1971, The Biochemical journal.

[12]  D. L. Lee The structure and composition of the helminth cuticle. , 1966, Advances in parasitology.

[13]  F. Greenwood,et al.  Preparation of Iodine-131 Labelled Human Growth Hormone of High Specific Activity , 1962, Nature.