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Journal of Clinical Microbiology, 11 1997, 2778-2781, Vol 35, No. 11
LM Teixeira, MG Carvalho, VL Merquior, AG Steigerwalt, DJ Brenner and RR Facklam
This study presents phenotypic and genotypic data for seven isolates of
Vagococcus fluvialis, including four strains recovered from human clinical
sources, one strain isolated from an environmental source, and two strains
isolated from pigs. On the basis of phenotypic characteristics, most
isolates were initially classified as "unidentified enterococci," because
they resembled atypical arginine- negative enterococcal species. All seven
strains as well as the type strain of V. fluvialis reacted with the
AccuProbe Enterococcus genetic probe. The seven isolates had virtually
indistinguishable whole-cell protein profiles that were similar to that of
the V. fluvialis type strain and distinct from those of Enterococcus and
Lactococcus species. DNA-DNA reassociation experiments confirmed that the
strains were V. fluvialis. They were 71% or more related to the V.
fluvialis type strain under optimum and stringent conditions, with 2.5% or
less divergence within related sequences. All strains were susceptible to
ampicillin, cefotaxime, trimethoprim-sulfamethoxazole, and vancomycin and
were resistant to clindamycin, lomefloxacin, and ofloxacin. Strain-
to-strain variation was observed in relation to susceptibilities to 18
other antimicrobial agents. Chromosomal DNA was analyzed by pulsed- field
gel electrophoresis (PFGE) after digestion with SmaI. Distinctive PFGE
patterns were generated, suggesting the nonclonal nature of V. fluvialis
strains. Although the number of strains was small, this report provides
molecular characterization of V. fluvialis and the first evidence of a
possible connection of this species with human infections.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Phenotypic and genotypic characterization of Vagococcus fluvialis, including strains isolated from human sources [In Process Citation]
Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Brazil. IMMMTML@microbio.ufrj.br
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