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Appl. Environ. Microbiol., Dec 1995, 4367-4373, Vol 61, No. 12
L Grisez and F Ollevier
The different serotyping systems, based on thermostable O antigens,
reported for Vibrio anguillarum and V. ordalii were compared by
quantitative agglutination, sodium dodecyl sulfate-polyacrylamide gel
electrophoresis, and subsequent silver staining or Western blotting
(immunoblotting) of purified lipopolysaccharide (LPS), using polyclonal
rabbit antisera. The results demonstrate that 16 different serotypes within
V. anguillarum (designated O1 to O16) can be distinguished. Each of these
serotypes is characterized by a distinct polysaccharide banding pattern, as
revealed by silver-stained gels of purified LPS. The comparative analysis
allowed a complete alignment of the different serotypes for the first three
serovars: O1, O2, and O3. Moreover, immunoblotting showed that strains
belonging to each of these serotypes had the same LPS banding pattern
independent of the origin of the strain. Serotype O2 contains different
subtypes, O2a and O2b. While no differences were apparent between these
subgroups in silver-stained gels, they could be separated by quantitative
agglutination (titer determination) or immunoblotting. V. ordalii, the
former biotype II of V. anguillarum, strongly reacts with anti-V.
anguillarum O2a antiserum. Strains of the two species can be separated on
the basis of different LPS profiles in the high-molecular-weight region of
silver-stained gels of purified LPS. The silver-stained LPS profiles of the
different serotypes of V. anguillarum that have been established are
provided for further comparison in the future.
Copyright © 1995, American Society for Microbiology
Comparative Serology of the Marine Fish Pathogen Vibrio anguillarum
Laboratory for Ecology and Aquaculture, Zoological Institute, K. U. Leuven, B-3000 Leuven, Belgium
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