Intraspecific Epitopic Variation in a Carbohydrate Antigen Exposed on the Surface of Trichostrongylus colubriformis Infective L3 Larvae

The carbohydrate larval antigen, CarLA, is present on the exposed surface of all strongylid nematode infective L3 larvae tested, and antibodies against CarLA can promote rapid immune rejection of incoming Trichostrongylus colubriformis larvae in sheep. A library of ovine recombinant single chain Fv (scFv) antibody fragments, displayed on phage, was prepared from B cell mRNA of field-immune sheep. Phage displaying scFvs that bind to the surface of living exsheathed T. colubriformis L3 larvae were identified, and the majority of worm-binding scFvs recognized CarLA. Characterization of greater than 500 worm surface binding phage resulted in the identification of nine different anti-CarLA scFvs that recognized three distinct T. colubriformis CarLA epitopes based on blocking and additive ELISA. All anti-CarLA scFvs were specific to the T. colubriformis species of nematode. Each of the three scFv epitope classes displayed identical Western blot recognition patterns and recognized the exposed surface of living T. colubriformis exsheathed L3 larvae. Surprisingly, each of the anti-CarLA scFvs was able to bind to only a subset of worms. Double-labelling indirect immunofluorescence revealed that the three classes of anti-CarLA scFvs recognize distinct, non-overlapping, T. colubriformis sub-populations. These results demonstrate that individual T. colubriformis L3 larvae display only one of at least three distinct antigenic forms of CarLA on their surface at any given time, and suggest that antigenic variation within CarLA is likely a mechanism of immune evasion in strongylid nematodes.

[1]  C. Shoemaker,et al.  Antibodies to surface epitopes of the carbohydrate larval antigen CarLA are associated with passive protection in strongylid nematode challenge infections , 2008, Parasite immunology.

[2]  C. Shoemaker,et al.  Three surface antigens dominate the mucosal antibody response to gastrointestinal L3-stage strongylid nematodes in field immune sheep. , 2007, International journal for parasitology.

[3]  A. Dell,et al.  Glycolipids as Receptors for Bacillus thuringiensis Crystal Toxin , 2005, Science.

[4]  S. Newton,et al.  Progress and new technologies for developing vaccines against gastrointestinal nematode parasites of sheep , 2003, Parasite immunology.

[5]  C. Shoemaker,et al.  Characterization of a 35‐kDa carbohydrate larval antigen (CarLA) from Trichostrongylus colubriformis; a potential target for host immunity , 2003, Parasite immunology.

[6]  C. Shoemaker,et al.  Immune rejection of Trichostrongylus colubriformis in sheep; a possible role for intestinal mucus antibody against an L3‐specific surface antigen , 2003, Parasite immunology.

[7]  D. Wakelin,et al.  Variation and immunity to intestinal worms , 2002, Parasitology.

[8]  R. Maizels,et al.  Variation and polymorphism in helminth parasites , 2002, Parasitology.

[9]  A. Read,et al.  Helminth immunogenetics: Why bother? , 1996, Parasitology today.

[10]  M. Brandon,et al.  Stage‐specific expression of surface molecules by the larval stages of Haemonchus contortus , 1996, Parasite immunology.

[11]  J. Crowther ELISA. Theory and practice. , 1995, Methods in molecular biology.

[12]  B. Ravindran,et al.  Bancroftian filariasis‐differential reactivity of anti‐sheath antibodies in microfilariae carriers , 1994, Parasite immunology.

[13]  C. Barnard,et al.  Understanding chronic nematode infections: evolutionary considerations, current hypotheses and the way forward. , 1992, International journal for parasitology.

[14]  E. Fraser,et al.  Heterogeneity in the expression of surface‐exposed epitopes among larvae of Ascaris lumbricoides , 1991, Parasite immunology.

[15]  E. Kabat,et al.  Sequences of proteins of immunological interest , 1991 .

[16]  B. Friguet,et al.  A convenient enzyme-linked immunosorbent assay for testing whether monoclonal antibodies recognize the same antigenic site. Application to hybridomas specific for the beta 2-subunit of Escherichia coli tryptophan synthase. , 1983, Journal of immunological methods.