SUMMARYAn analysis of genotype was made for representative strains of Salmonella dublin. The collection consisted primarily of strains isolated from humans in England and WVales. and were of both intestinal and extra-intestinal origin. Three genetic elements were characterized by DNA hybridization. They were the spvBC genes, extrachromosomal virulence determinants, the salmonella-specific insertion sequence IS200, and the 168 ribosomal RNA genes, a phylogenetic marker. Two clones of S. dublin (SdRI and SdRII) which shaied an identical IS200 profile, were identified on the basis of restriction fragment length polymorphism at the 168 rRNA locus. With one exception, all strains harboured a 52 MDa plasmid which contained a conserved 37 kbp Hind III fragment homologous to the spvBC mouse-virulence genes of S. typhimuriurn. However, a single plasmid-free strain of SdRI, isolated from a patient with septicaemia exhibited no spv homology. In SdRI there was no observable genotype distinction between strains causing gastroenteritis or bacteraemia. In contrast, none of the strains of SdRII were from cases of bacteraemia, and all human isolates of this clone were from cases of gastroenteritis. IN Phenotypic subtyping with bacteriophages has provided highly discriminatory schemes for salinonella serovars of epidemniological imnportance such as S. enteritidis, S. typhinurium, and S. typhi. However, in England and Wales the relatively low incidence of S. dublin in humans has not justified the development of such a scheme for this serovar. Plasmid profile typing is also inappropriate for S. dublin, since most isolates contain a single large serotype-specific plasmid of 52 inegadaltons (AIDa) [3] implicated in virulence of the organism for BALB c mice. A * Corresponlding authlor.