Affiliation:
1. Central Laboratory of Bacteriology, University Hospital, Geneva,1 and
2. Bacteriology Laboratory, University Clinics, Basel,2 Switzerland
Abstract
ABSTRACT
Between August 1994 and September 1996, 28 glycopeptide-resistant enterococci (GRE) were isolated from 8 infected patients and 11 intestinal carriers hospitalized at the University Hospital of Geneva. Identification to the species was made by both phenotypic (API 20 STREP and Rapid ID 32 STREP systems, and Vitek Gram Positive Identification Card) and genotypic methods using a multiplex PCR assay developed also for the determination of the genotype of glycopeptide resistance (
vanA
,
vanB
,
vanC1
, and
vanC2-C3
genes). Fifteen isolates were identified as
Enterococcus faecium
, 8 as
E. gallinarum
, 4 as
E. faecalis
, and 1 as
E. hirae
. All of the phenotypic identification methods failed to differentiate some isolates of
E. gallinarum
from
E. faecium
, or vice versa. Both
vanA
(
n
= 18) and
vanB
(
n
= 4) glycopeptide resistance genotypes were found. For the first time, the
vanB
determinant was found in two isolates of
E. gallinarum
. Two patients were colonized by two different species containing the
vanA
gene and one by two different species containing the
vanB
gene. All
vanA
isolates were highly resistant to both vancomycin and teicoplanin except for three isolates which were susceptible to teicoplanin. Molecular typing by pulsed-field gel electrophoresis showed identical or similar patterns among
E. faecium
isolates with the
vanA
gene in five patients for whom the epidemiological link could not be always elucidated. This study emphasizes the necessity of utilizing both phenotypic and genotypic methods to characterize GRE.
Publisher
American Society for Microbiology
Cited by
58 articles.
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