Affiliation:
1. Department of Bacterial Pathogenesis and Infection Control, National Institute of Infectious Diseases, Tokyo
2. Program in Radiological and Medical Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan
3. Central Clinical Laboratory, Kagoshima Municipal Hospital, Kagoshima
Abstract
ABSTRACT
Klebsiella pneumoniae
strain KG525, which showed high-level resistance to broad-spectrum cephalosporins, was isolated from the neonatal intensive care unit (NICU) of a Japanese hospital in March 2002. The ceftazidime resistance of strain KG525 was transferable to
Escherichia coli
CSH-2 by conjugation. Cloning and sequence analysis revealed that production of a novel extended-spectrum class A β-lactamase (pI 7.0), designated GES-3, which had two amino acid substitutions of M62T and E104K on the basis of the sequence of GES-1, was responsible for resistance in strain KG525 and its transconjugant. The
bla
GES-3
gene was located as the first gene cassette in a class 1 integron that also contained an
aacA1-orfG
fused gene cassette and one unique cassette that has not been described in other class 1 integrons and ended with a truncated 3′ conserved segment by insertion of IS
26
. Another five ceftazidime-resistant
K. pneumoniae
strains, strains KG914, KG1116, KG545, KG502, and KG827, which were isolated from different neonates during a 1-year period in the same NICU where strain KG525 had been isolated, were also positive for GES-type β-lactamase genes by PCR. Pulsed-field gel electrophoresis and enterobacterial repetitive intergenic consensus-PCR analyses displayed genetic relatedness among the six
K. pneumoniae
strains. Southern hybridization analysis with a GES-type β-lactamase gene-specific probe showed that the locations of
bla
GES
were multiple and diverse among the six strains. These findings suggest that within the NICU setting genetically related
K. pneumoniae
strains carrying the
bla
GES
gene were ambushed with genetic rearrangements that caused the multiplication and translocation of the
bla
GES
gene.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
56 articles.
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