K. Pedersen et al., Clonality of Vibrio anguillarum strains isolated from fish from the Scandinavian countries, Sweden, Finland and Denmark, J APPL MICR, 86(2), 1999, pp. 337-347
In order to investigate whether outbreaks of vibriosis in the Baltic region
were caused by the spread of certain pathogenic clones, 291 Vibrio anguill
arum isolates from Finland (n = 156), Sweden (n = 88) and Denmark (n = 47)
were studied with respect to serogroup, ribotype, plasmid content, and bioc
hemical phenotypes as expressed with the PhenePlate (PhP) typing system. Fo
r comparison, 54 V. anguillarum serogroup O1 from other countries worldwide
were included. Most isolates from Finland, Sweden and Denmark belonged to
serogroup O1 (255), followed by O2 (30). Four Finnish isolates cross-reacte
d strongly with antisera against two new serogroups VaNT2 and VaNT4, wherea
s two strains were non-typeable. The serogroup O1 isolates displayed ten di
fferent ribotype patterns, whereas the other strains were considerably more
diverse with respect to ribotypes. Most of the O1 isolates carried the 67
kb virulence plasmid and a group of Finnish isolates, in addition, carried
an 86 kb plasmid. Additional plasmids with molecular weights of 63, 76, 135
or 260-290 kb were found in single O1 isolates. With few exceptions, strai
ns of serogroup O2 either had no plasmids or carried one or two Small plasm
ids. PhenePlate typing revealed considerable diversity within the species,
serogroup O1 being the most homogeneous. A few PhP types were dominant, whe
reas other types were observed only in one to four isolates. The prevalence
of the different types changed significantly from one year to another but
in Finland, one clonal lineage became increasingly important from 1992 (20%
of isolates) to 1996 (80%). Remaining clones were mostly restricted to spe
cific geographic areas. By cluster analysis, it was demonstrated that most
of the isolates from Finland, Sweden and Denmark belonged to two clusters,
and most of the strains from Southern Europe fell into two other, distinct
clusters. Most isolates from the UK, North America, Chile and Tasmania grou
ped together in a distinct cluster. For the typing of V. anguillarum, O-ser
otyping should be the primary method. For isolates belonging to serogroups
other than O1, plasmid profiling in combination with ribotyping gives a ver
y good discrimination between strains, whereas for serogroup O1, another me
thod is required. It is concluded that PhP typing is a tool that provides a
good discrimination between O1 isolates.