Affiliation:
1. Veterans Administration Hospital and the Departments of Medicine and Microbiology, University of Tennessee, Memphis, Tennessee 38104
Abstract
M protein of group A streptococci was extracted by mild peptic digestion. Optimal amounts of type-specific M protein were released after 20 min of digestion with 0.02 mg of pepsin per ml at pH 5.8. Immunological analysis revealed that, unlike conventional HCl extracts, pepsin extracts lacked the surface C carbohydrate antigen and contained less non-type-specific, heat-stable cellular antigens; they also lacked detectable heat-labile T protein. Similar to HCl extracts, however, the pepsin-extracted M protein precipitated homologous-type M antisera and inhibited type-specific opsonization of homologous group A streptococci. Furthermore, the pepsin extract was capable of inducing type-specific opsonic M antibody in rabbits. This method may provide a useful initial step in the purification of M protein by reducing contaminating antigens.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Reference21 articles.
1. Delayed hypersensitivity to purified streptococcal M protein in guinea pigs and in man;Beachey E. H.;J. Immunol.,1969
2. Type-specific inhibition of preopsonization versus immunoprecipitation by streptococcal M proteins;Beachey E. H.;Infect. Immunity,1973
3. Studies of antibodies to non-type-specific antigens associated with streptococcal M protein in the sera of patients with rheumatic fever;Beachey E. H.;J. Immunol.,1973
4. Toxic effects of streptococcal Mi protein on platelets and polymorphonuclear leukocytes in human blood;Beachey E. H.;J. Exp. Med.,1971
5. Mediation of cytotoxic effects of streptococcal M protein by nontype-specific antibody in human sera;Beachey E. H.;J. Clin. Invest.,1973
Cited by
59 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献