Affiliation:
1. Hospital Infections Program1 and
2. Division of Bacterial and Mycotic Diseases,2 National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, and
3. Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil 219413
Abstract
ABSTRACT
The VanC phenotype, as found in
Enterococcus gallinarum
,
E. casseliflavus
, and
E. flavescens
, is characterized by intrinsic low-level resistance to vancomycin. The nucleotide sequences of the
vanC-1
gene in
E. gallinarum
, the
vanC-2
gene in
E. casseliflavus
, and the
vanC-3
gene in
E. flavescens
have been reported, although there is some disagreement as to whether
E. flavescens
is a legitimate enterococcal species. Previous attempts to differentiate the
vanC-2
and
vanC-3
genes by PCR analysis have been unsuccessful. The purpose of the present study was to detect and differentiate the three
vanC
determinants and examine the distribution of these genes in a collection of both typical and atypical enterococci. The 796-bp
vanC-1
PCR product was amplified only from
E. gallinarum
isolates. As expected, due to the extensive homology in the
vanC-2
and
vanC-3
gene sequences, all of the
E. casseliflavus
and
E. casseliflavus/flavescens
isolates produced the 484-bp
vanC-2
PCR product, although the
E. gallinarum
isolates were negative. Only the
E. casseliflavus/flavescens
isolates produced the 224-bp
vanC-3
product. Using the three sets of primers, we were able to detect and distinguish the
vanC-1
,
vanC-2
, and
vanC-3
genes from both typical and atypical enterococci strains. Antimicrobial susceptibility tests and analysis of genomic DNA by pulsed-field gel electrophoresis were also performed, but the results indicated that they were not able to distinguish among strains possessing the three
vanC
genotypes.
Publisher
American Society for Microbiology
Cited by
79 articles.
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