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Infect Immun. 1979 August; 25(2): 615-626

Characterization of the Antigenic Determinants of Cholera Toxin Subunits

Daiel E. Markel^1,, Kelly E. Hejtmancik^1,, Johnny W. Peterson¹, Frank B. Martin¹ and Alexander Kurosky²

¹ Department of Microbiology, University of Texas Medical Branch, Galveston, Texas 77550
² Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston, Texas 77550

ABSTRACT

The antigenic specificity of purified preparations of A subunit, B subunit, chain, and chain of cholera toxin was studied by double immunodiffusion and radioimmunoassay with antisera produced in rabbits and mice. Rabbits immunized with A subunit produced serum antibodies which were capable of binding radiolabeled A subunit, chain, and B subunit. Rabbits immunized with chain produced serum antibodies that would bind radiolabeled chain and A subunit. Rabbits immunized with the B subunit produced serum antibodies monospecific for the B subunit. The chain did not elicit measurable antibodies in rabbits or mice as evidenced by radioimmunoassay or double immunodiffusion. A sensitive competitive radioimmunoassay was developed in which the B subunit could inhibit binding of radiolabeled A subunit and chain with either antisera prepared against A subunit or chain. Neither the A subunit nor the chain could inhibit binding of B subunit with the antiserum prepared against B subunit. In addition, selected elution fractions obtained during A- and B-subunit purification were used to immunize groups of mice. Mice responded to immunization with the elution fractions of A subunit by producing anti-A-subunit and anti-B-subunit serum antibody responses, whereas mice immunized with elution fractions of B subunit produced only antibodies specific for the B subunit. An equimolar amount of the two resulting protein peaks was used to immunize two groups of rabbits. Rabbits immunized with A subunit, produced a serum anti-B subunit response equal to that of rabbits immunized with the B subunit. Rabbits immunized with equimolar concentrations of A and B subunits were observed to be equally protected against intestinal loop challenge with Vibrio cholerae Inaba V86. The A subunit, not the B subunit, was biologically active when tested by the S49 mouse lymphosarcoma cell test. These studies provide additional evidence supporting the hypothesis that the A subunit, specifically of chain, of cholera toxin contains antigenic determinants in common with the B subunit.

Present address: Department of Microbiology and Immunology, Oral Roberts University School of Medicine, Tulsa, OK 74171.

Present address: Department of Surgery, University of Texas Medical Branch, Galveston, TX 77550.