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Developmentally regulated expression of a Haemonchus contortus surface antigen
1Department of Veterinary Science, University of Melbourne, Parkville, Victoria, Australia.
International Journal for Parasitology
|June 1, 1996
Summary
Antibody-secreting cell (ASC) probes revealed distinct Haemonchus contortus antigens during development. A 70-90 kDa antigen in L3 larvae is related to a 28-31 kDa molecule in earlier stages, suggesting a complex assembly process.
Area of Science:
- Veterinary Parasitology
- Molecular Biology
- Immunology
Background:
- Haemonchus contortus is a significant gastrointestinal nematode parasite of livestock.
- Understanding parasite antigen expression is crucial for vaccine development.
- Antibody-secreting cells (ASCs) can be used as probes to identify parasite antigens recognized by the host immune system.
Purpose of the Study:
- To identify and characterize Haemonchus contortus antigens expressed across different life cycle stages.
- To investigate the relationship between a major 3rd-stage larval antigen and molecules expressed in earlier developmental stages.
Main Methods:
- Screening of all Haemonchus contortus life cycle stages using antibody-secreting cell (ASC) probes from immune sheep.
- Characterization of antigen molecular weights using SDS-PAGE and Western blotting.
- Generation of antisera against purified antigens and elution of antibodies from specific molecular weight regions.
Main Results:
- A 70-90 kDa antigen was predominantly expressed in 3rd-stage larvae (L3).
- A 28-31 kDa molecule was recognized by ASC probes in earlier larval stages (L2).
- Antisera against the 70-90 kDa antigen reacted with the 28-31 kDa molecule in L2, indicating a shared antigenic determinant.
Conclusions:
- The 70-90 kDa surface antigen of H. contortus L3 larvae is synthesized as a lower molecular weight precursor (28-31 kDa) in earlier larval stages.
- This precursor molecule is assembled into a higher molecular weight complex via non-reducible covalent bonds.
- This finding provides insights into the post-translational modification and assembly of parasite antigens, relevant for targeted intervention strategies.