Premium
Attempts to immunize sheep against Haemonchus contortus using a cocktail of recombinant proteases derived from the protective antigen, H‐gal‐GP
Author(s) -
CACHAT E.,
NEWLANDS G. F. J.,
EKOJA S. E.,
MCALLISTER H.,
SMITH W. D.
Publication year - 2010
Publication title -
parasite immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.795
H-Index - 75
eISSN - 1365-3024
pISSN - 0141-9838
DOI - 10.1111/j.1365-3024.2010.01208.x
Subject(s) - haemonchus contortus , biology , recombinant dna , proteases , antigen , adjuvant , microbiology and biotechnology , escherichia coli , vaccination , immunogenicity , antibody , virology , immunity , immunology , immune system , helminths , enzyme , biochemistry , gene
Summary The objective of this study was to determine whether an antigen cocktail containing recombinantly expressed versions of most of the protective proteases of H‐gal‐GP, a known protective antigen from Haemonchus contortus , would confer any protection to lambs in a vaccine‐challenge trial. Haemonchus contortus metalloendopeptidases, MEP1, MEP3 and MEP4, were expressed as soluble recombinant proteins in insect cells, but attempts to express the H. contortus aspartyl proteases, PEP1 and PEP2, by the same techniques were not successful. Recombinant H. contortus PEP1 was therefore expressed in Escherichia coli and refolded. Groups of sheep were immunized thrice with either native H‐gal‐GP, a cocktail of recombinantly expressed proteins (rMEP1, rMEP3, rMEP4 and rPep1), or adjuvant only (QuilA in PBS). All sheep were challenged with 5000 infective larvae 1 week after the final vaccination. High levels of serum antibodies that recognized H‐gal‐GP were detected in both the native antigen and recombinant cocktail‐immunized groups by the time of challenge, but protective immunity was only observed in the group immunized with native H‐gal‐GP.