A temperate phage, +CTX, is a cytotoxin-converting phage of Pseudomonas aeruginosa. In this study, we characterized the lipopolysaccharide (LPS) structures of 4CTX-resistant mutants derived from 4CTX-sensitive strains. 4CTX infectivity was neutralized by LPS preparations derived from sensitive strains but not by those from resistant strains. 4CTX-resistant mutants had lower-molecular-weight rough (R)-type LPS than the parental strains and lacked the reactivity of some anti-LPS core monoclonal antibodies. Some LPS core components were lacking or significantly decreased in the resistant mutants. These results suggested that a receptor site of the cytotoxin-converting phage +CTX was the LPS core region and that especially L-rhamnose and D-glucose residues in the outer core were involved in phage binding. The host range of +CTX was nearly 0-serotype dependent, probably because of the diversity of the LPS core structure among P. aeruginosa strains.+CTX bound to most strains of Homma serotypes A, G, and I but not to strains of serotypes B and E.Furthermore, we found that a genetic locus specifying 4)CTX sensitivity (and consequently participating in the biosynthesis of part of the LPS core) existed in or near the locus participating in the determination of 0-serotype specificity (somA), which has been mapped between leu-10 and eda-9001. 4CTX, as well as anti-LPS core monoclonal antibodies, will be a good tool for structural characterization of the P. aeruginosa LPS core region.Pseudomonas aeruginosa cytotoxin shows a wide range of cytotoxic activity against eukaryotic cells, especially leukocytes (9,22,31). Unlike other toxins and enzymes produced by P. aeruginosa, cytotoxin is not secreted into the culture medium. It is produced as a cell-associated procytotoxin, released into the medium during cell lysis, and then converted to an active cytotoxin by C-terminal processing (8,9,31).In previous studies (6,7,11), it was found that the gene encoding cytotoxin, clx, existed only in two of about 400 P. aeruginosa strains from various sources and that in both strains the genes existed on the genomes of the prophages. Furthermore, both of the bacteriophages isolated, which were phylogenetically closely related to each other (11), actually converted P. aeruginosa strains to cytotoxin producers by their lysogenization (7, 11). 4~CTX is one of the cytotoxin-converting phages isolated from strain PA158, a strong cytotoxin producer which has been widely used for the study of cytotoxin.Since 4~CTX could infect only some but not all P. aeruginosa strains (reference 6 and this study), the host range of 4)CTX seemed to depend on the presence of a specific receptor on the bacterial cell surface. However, the receptor site for CrX has not been revealed yet. Recently, we and others found that bacteriophage~CTX is related to the R-type pyocins (11). The finding suggested that, as has been proposed for the R-type pyocins (25), lipopolysaccharide (LPS), not outer membrane protein, could be a receptor site for XCTX. The present study examin...