of Neisseriu gonorrhoeue. Characterization of rabbit hyperimmune antisera by line-rocket immunoelectrophoresis for the use in co-agglutination. Acta path. microbiol. scand. Sect. B, 88: 17-26, 1980.The co-agglutination (COA) and line-rocket immunoelectrophoresis (L-RIE) techniques were investigated for the serological classification of Neisseriu gonorrhoeae. COA with absorbed sera was found to demonstrate ))strain-specific(( as well as cross-reacting antigens. The results were dependent on the immunizing, absorbing and agglutinating properties of a particular strain. Heated (I00 OC) whole cells were found to be more reactive in the COA tests than untreated or formalin-fixed organisms. It was possible by L-RIE to compare the antigenic relationship between at least 20 strains in a single test run. This technique was applied on the 16 major outer membrane protein (MOMP) reference strains, which could then be divided into two separate groups with regard to cross-reacting antigens. Based on the findings by the L-RIE tests, selective absorptions of antibodies were performed for use in preparation of COA reagents. It was found that the reactions of these reagents with the MOMP reference strains could be assigned to three different antigenic classes. Reagents prepared for these classes are proposed as a basis for serological classification of Neisseriu gonorrhoeue.Serological classifications of the various bacterial genera and species such as Salmonellae, Shigellae, Escherichia coli, and Neisseria meningitidis have greatly aided the understanding of the epidemiology and pathogenesis of infections with these organisms, as well as their ecology. Such classificationhas not yet been worked out and accepted for Neisseria gonorrhoeae, despite serious attempts by several investigators. In these studies viable or killed whole gonococcal cells were used in standard agglutination ( 1 7, 1 91, complement fixation ( I 4), and direct or indirect immunofluorescence (IFL) (6,13,18). Other investigators used gonococcal cell fractions in various stages of purification in agar gel diffusion (6, 9, 101, passive haemagglutination o r haemolysis ( I , 4, 12). All the published data demonstrated the serological heterogeneity of these organisms.We recently reported the results of co-agglutination (COA) and indirect IFL in demonstrating strain-specific antigens of N. gonorrhoeae by the use of cross-absorbed antibodies (8). The results correlated well with those obtained by rocket-line immunoelectrophoresis with antigen-containing intermediate agar gel. Our findings also indicated that