DIFFERENTIATION OF SHEWANELLA-PUTREFACIENS AND SHEWANELLA-ALGA ON THEBASIS OF WHOLE-CELL PROTEIN PROFILES, RIBOTYPING, PHENOTYPIC CHARACTERIZATION, AND 16S RIBOSOMAL-RNA GENE SEQUENCE-ANALYSIS
Bf. Vogel et al., DIFFERENTIATION OF SHEWANELLA-PUTREFACIENS AND SHEWANELLA-ALGA ON THEBASIS OF WHOLE-CELL PROTEIN PROFILES, RIBOTYPING, PHENOTYPIC CHARACTERIZATION, AND 16S RIBOSOMAL-RNA GENE SEQUENCE-ANALYSIS, Applied and environmental microbiology, 63(6), 1997, pp. 2189-2199
Seventy-six presumed Shewanella putrefaciens isolates from fish, oil d
rillings, and clinical specimens, the type strain of Shewanella putref
aciens (ATCC 8071), the type strain of Shewanella alga (IAM 14159), an
d the type strain of Shewanella hanedai (ATCC 33224) were compared by
several typing methods. Numerical analysis of sodium dodecyl sulfate-p
olyacrylamide gel electrophoresis of whole-cell protein and ribotyping
patterns showed that the strains were separated into two distinct clu
sters with 56% +/- 10% and 40% +/- 14% similarity for whole-cell prote
in profiling and ribotyping, respectively. One cluster consisted of 26
isolates with 52 to 55 mol% G + C and included 15 human isolates, mos
tly clinical specimens, 8 isolates from marine waters, and the type st
rain of S. alga. This homogeneous cluster of mesophilic, halotolerant
strains was by all analyses identical to the recently defined species
S. alga (U. Simidu et at., Int. J. Syst. Bacteriol. 40:331-336, 1990).
Fifty-two typically psychrotolerant strains formed the other, more he
terogeneous major cluster, with 43 to 47 mol% G + C. The type strain o
f S. putrefaciens was included in this group. The two groups were conf
irmed by 16S rRNA gene sequence analysis. It is concluded that the iso
lates must be considered two different species, S. alga and S. putrefa
ciens, and that most mesophilic isolates formerly identified as S. put
refaciens belong to S. alga. The ecological role and potential pathoge
nicity of S. alga can be evaluated only if the organism is correctly i
dentified.