Affiliation:
1. Center for the Study of Emerging and Reemerging Pathogens,1
2. Division of Infectious Diseases, Department of Internal Medicine,2 and
3. Department of Microbiology and Molecular Genetics,3 The University of Texas Medical School, Houston, Texas 77030
Abstract
ABSTRACT
Enterococci are usually susceptible in vitro to trimethoprim; however, high-level resistance (HLR) (MICs, >1,024 μg/ml) has been reported. We studied
Enterococcus faecalis
DEL, for which the trimethoprim MIC was >1,024 μg/ml. No transfer of resistance was achieved by broth or filter matings. Two different genes that conferred trimethoprim resistance when they were cloned in
Escherichia coli
(MICs, 128 and >1,024 μg/ml) were studied. One gene that coded for a polypeptide of 165 amino acids (MIC, 128 μg/ml for
E. coli
) was identical to
dfr
homologs that we cloned from a trimethoprim-susceptible
E. faecalis
strain, and it is presumed to be the intrinsic
E. faecalis dfr
gene (which causes resistance in
E. coli
when cloned in multiple copies); this gene was designated
dfrE
. The nucleotide sequence 5′ to this
dfr
gene showed similarity to thymidylate synthetase genes, suggesting that the
dfr
and
thy
genes from
E. faecalis
are located in tandem. The
E. faecalis
gene that conferred HLR to trimethoprim in
E. coli
, designated
dfrF
, codes for a predicted polypeptide of 165 amino acids with 38 to 64% similarity with other dihydrofolate reductases from gram-positive and gram-negative organisms. The nucleotide sequence 5′ to
dfrF
did not show similarity to the
thy
sequences. A DNA probe for
dfrF
hybridized under high-stringency conditions only to colony lysates of enterococci for which the trimethoprim MIC was >1,024 μg/ml; there was no hybridization to plasmid DNA from the strain of origin. To confirm that this gene causes trimethoprim resistance in enterococci, we cloned it into the integrative vector pAT113 and electroporated it into RH110 (
E. faecalis
OG1RF::Tn
916
ΔEm) (trimethoprim MIC, 0.5 μg/ml), which resulted in RH110 derivatives for which the trimethoprim MIC was >1,024 μg/ml. These results indicate that
dfrF
is an acquired but probably chromosomally located gene which is responsible for in vitro HLR to trimethoprim in
E. faecalis
.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
56 articles.
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