Abstract
A rapid slide agglutination test has been developed for the identification of Neisseria gonorrhoeae that are primarily detected as oxidase-positive colonies in gonococcal cultures. The technique is based on the specific nonimmune reactivity between the Fc portion of immunoglobulin (Ig)G and staphylococcal protein A. IgG molecules adsorbed to stabilized staphylococci will thereby become oriented with their antigen-reactive sites that are directed outwards. Protein A-containing staphylococci with unabsorbed anti-gonococcal antibodies gave positive co-agglutination reactions with gonococci but also with meningococci, some Moraxella, Haemophilus, and Pseudomonas strains. These crossreactions were eliminated by absorption of the anti-gonococcal antiserum with meningococcal and Moraxella organisms prior to the coating of reagent staphylococci. In the routine culture diagnosis of N. gonorrhoeae the use of specific gonococcal reagent staphylococci gave concordant results with fermentation procedures and immunofluorescent techniques.
MeSH Terms
Adsorption
Agglutination Tests
Animals
Bacterial Proteins
Bacteriological Techniques
Binding Sites, Antibody
Cross Reactions
Evaluation Studies as Topic
Fermentation
Fluorescent Antibody Technique
Haemophilus/immunology
Haemophilus influenzae/immunology
Immunoglobulin Fc Fragments
Methods
Moraxella/immunology
Neisseria/immunology
Neisseria gonorrhoeae/enzymology,immunology,isolation & purification
Oxidoreductases/biosynthesis
Pseudomonas/immunology
Rabbits/immunology
Staphylococcus
Chemicals
Bacterial Proteins
Immunoglobulin Fc Fragments
Oxidoreductases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Danielsson D
Kronvall G
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17 references, click to expand
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