Integron Carrying a Novel Metallo-β-Lactamase Gene, bla IMP-16 , and a Fused Form of Aminoglycoside-Resistant Gene aac(6′)-30/aac(6′)-Ib′ : Report from the SENTRY Antimicrobial Surveillance Program
Open Access
- 1 December 2004
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 48 (12), 4693-4702
- https://doi.org/10.1128/aac.48.12.4693-4702.2004
Abstract
Since January 2002 Pseudomonas sp. strains resistant to carbapenems and ceftazidime have been routinely screened as part of the SENTRY Antimicrobial Surveillance Program for metallo-β-lactamase production, and their resistance determinants have been analyzed. Pseudomonas aeruginosa index strain 101-4704, which harbors a novel blaIMP variant, blaIMP-16, was isolated in April 2002 from a 60-year-old man in Brasília, Brazil. blaIMP-16 was found on the chromosome of the P. aeruginosa index strain, and the deduced amino acid sequence (IMP-16) showed the greatest identities to IMP-11 (90.3%) and IMP-8 (89.5%). Sequence analysis revealed that blaIMP-16 was associated with a class 1 integron, which also encoded aminoglycoside-modifying enzymes. Downstream of blaIMP-16 resided an open reading frame, which consisted of a new aminoglycoside-modifying gene, namely, aac(6′)-30, which was fused with aac(6′)-Ib′. The amino acid sequence of the aac(6′)-30 putative protein showed the most identity (52.7%) to the sequence of AAC(6′)-29b described previously. The fourth gene cassette constituted aadA1. The steady-state kinetics of IMP-16 demonstrated that the enzyme preferred cephalosporins and carbapenems to penicillins. The main functional difference observed among the kinetic values for IMP-16 compared to those for other IMPs was a lack of cefoxitin hydrolysis and a lower kcat/Km value for imipenem (0.36 μM−1 · s−1). This report further emphasizes the spread of metallo-β-lactamase genes and their close association with various aminoglycoside resistance genes.Keywords
This publication has 52 references indexed in Scilit:
- First Isolation of bla VIM-2 in Latin America: Report from the SENTRY Antimicrobial Surveillance ProgramAntimicrobial Agents and Chemotherapy, 2004
- Emergence of an IMP-like metallo-enzyme in an Acinetobacter baumannii clinical strain from a Brazilian teaching hospitalDiagnostic Microbiology and Infectious Disease, 2003
- Molecular characterization ofblaIMP-5, a new integron-borne metallo-β-lactamase gene from anAcinetobacter baumanniinosocomial isolate in PortugalFEMS Microbiology Letters, 2002
- Detection of a Variant Metallo-β-Lactamase, IMP-10, from Two Unrelated Strains of Pseudomonas aeruginosa and an Alcaligenes xylosoxidans StrainAntimicrobial Agents and Chemotherapy, 2002
- Novel Mechanism of Hydrolysis of Therapeutic β-Lactams byStenotrophomonas maltophilia L1 Metallo-β-lactamasePublished by Elsevier ,2001
- Standard Numbering Scheme for Class B β-LactamasesAntimicrobial Agents and Chemotherapy, 2001
- Kinetic and Mutagenic Characterization of the Chromosomally Encoded Salmonella enterica AAC(6‘)-Iy Aminoglycoside N-AcetyltransferaseBiochemistry, 2001
- Amino Acid Substitutions in a Variant of IMP-1 Metallo-β-LactamaseAntimicrobial Agents and Chemotherapy, 2000
- Characterization of the aac(6′)-Ik gene of Acinetobacter sp. 6FEMS Microbiology Letters, 1994
- A spontaneous point mutation i theaac(6′)-lb′gene results in altered substrate specificity of aminoglycoside 6′-N-acetyltransferase of aPseudomonas fluorescensstrainFEMS Microbiology Letters, 1994