The validity and distinctiveness of Vibrio anguillarum (= Listonella a
nguillara), V. (= Photobacterium) damsela, V. ordalii and V. salmonici
da was confirmed. However, strains received as V. cholerae and V. sple
ndidus were heterogeneous. Ribotyping, phenotypic (BIOLOG-GN fingerpri
nts and API 20E profiles), chemotaxonomic (lipopolysaccharide [LPS] an
d outer membrane proteins [OMP]), serogrouping and plasmid profiling d
ata were not always congruent. V. anguillarum isolates were recovered
in a single ribotype cluster, but many serogroups. There was little va
riation in OMP profiles, but not so for LPS profiles and plasmid compo
sition. Heterogeneity was recorded in the phenotypic characters, parti
cularly with the API 20E rapid identification system. V. damsela displ
ayed heterogeneity by ribotyping, but homogeneity by BIOLOG-GN fingerp
rints and API 20E profiles. Four serogroups were defined, but only one
LPS profile was recognised. V. ordalii was homogeneous by ribotyping,
serogrouping and plasmid profiling, was accommodated in two LPS group
s, but was more heterogeneous by BIOLOG-GN and API 20E. Despite its mo
re exacting cultural requirements, V. salmonicida autoagglutinated and
could not be serogrouped, but was accommodated in a single LPS group
showing a profile associated with rough strains, and contained plasmid
s of 4.7 and 42 kb. Heterogeneity was recorded with the API 20E rapid
identification system.