Comparison of methods for the immunological identification of Neisseria gonorrhoeae in clinical specimens using commercially-obtained reagents.

Neither an immunofluorescent nor a co-agglutination method was adequately sensitive for the detection of Neisseria gonorrhoeae when commercially-obtained reagents were used to test oxidase positive organisms taken directly from Transgrow medium. The sensitivity of co-agglutination, the better of the two methods, was improved from 83% to 96% when organisms were subcultured for colony isolation prior to identification. False positive results were obtained with both methods.