Affiliation:
1. Unité des Agents Antibactériens, Institut Pasteur, 75724 Paris Cedex 15
2. Institut Pasteur d'Ho Chi Minh Ville, Ho Chi Minh City, Vietnam
3. Centre d'Etude Pharmaceutiques, ChÂtenay-Malabry
4. Service de Bactériologie, Hôpital Tenon, U.F.R Saint-Antoine 75970 Paris Cedex 20, France
Abstract
ABSTRACT
Among 730
Escherichia coli
, 438
Klebsiella pneumoniae
, and 141
Proteus mirabilis
isolates obtained between September 2000 and September 2001 in seven hospitals in Ho Chi Minh City, Vietnam, 26.6% were resistant to ceftazidime, 30% were resistant to cefotaxime, 31.5% were resistant to ceftriaxone, 15.9% were resistant to cefoperazone, and 6% were resistant to cefepime. Resistance to imipenem was found in 5.6% of the isolates. In 55 strains producing extended-spectrum β-lactamases (32
E. coli
isolates, 13
K. pneumoniae
isolates, and 10
P. mirabilis
isolates), structural genes for VEB-1 (25.5%), CTX-M (25.5%), SHV (38.1%), and TEM (76.3%) enzymes were detected alone or in combination. Sequencing of the PCR products obtained from the
K. pneumoniae
isolates revealed the presence of
bla
VEB-1
,
bla
CTX-M-14
,
bla
CTX-M-17
,
bla
SHV-2
, and
bla
TEM-1
. Molecular typing of the strains with a similar resistance phenotype to broad-spectrum cephalosporins indicated polyclonal spread. IS
Ecp1
was presumably responsible for dissemination of the
bla
CTX-M-like
gene.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
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Klebsiella pneumoniae
Encoding Extended-Spectrum β-Lactamase CTX-M-17
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