Characterization of the aac(6')-Ib gene encoding an aminoglycoside 6'-N-acetyltransferase in Pseudomonas aeruginosa BM2656
- 1 July 1993
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 37 (7), 1456-1462
- https://doi.org/10.1128/aac.37.7.1456
Abstract
Pseudomonas aeruginosa BM2656 was resistant to tobramycin and susceptible to gentamicin and amikacin by disk diffusion testing. This unusual resistance was not transferable by conjugation to Escherichia coli or P. aeruginosa PAO38, and plasmid DNA was not detected in this strain. A 0.9-kb fragment harboring the tobramycin resistance gene was cloned from BM2656 into pUC18, generating pAT129. Analysis for aminoglycoside-modifying activity in extracts of BM2656 and E. coli harboring pAT129 indicated that tobramycin resistance was due to synthesis of an aminoglycoside 6'-N-acetyltransferase type I [AAC(6')-I] enzyme which modified amikacin and tobramycin. Although amikacin was acetylated, the bactericidal synergism of this aminoglycoside with ceftazidime against BM2656 was minimally affected. The sequence of the DNA fragment was determined. It contained an aac (6')-Ib-like gene and was located downstream from a conserved region related to Tn21. The translated sequence of this aac(6')-Ib gene possessed 99.2% identity with the putative products of the aac(6')-Ib gene cassettes from Serratia marcescens and Klebsiella pneumoniae and 69% identity with the putative aacA(6')-II gene product from P. aeruginosa. We conclude that an aac(6')-Ib gene has spread to the chromosome of P. aeruginosa, probably by transposition.Keywords
This publication has 23 references indexed in Scilit:
- Site‐specific insertion of genes into integrons: role of the 59‐base element and determination of the recombination cross‐over pointMolecular Microbiology, 1991
- Isolation, characterization, and DNA sequence analysis of an AAC(6')-II gene from Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1989
- A novel family of potentially mobile DNA elements encoding site‐specific gene‐integration functions: integronsMolecular Microbiology, 1989
- Structure and function of hot spots providing signals for site‐directed specific recombination and gene expression in Tn21 transposonsMolecular Microbiology, 1989
- Cloning and characterization of an AAC(6′) gene from Serratia marcescensJournal of Antimicrobial Chemotherapy, 1988
- Transferable amikacin resistance in Acinetobacter spp. due to a new type of 3'-aminoglycoside phosphotransferaseAntimicrobial Agents and Chemotherapy, 1988
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Activity of the hybrid trp-lac (tac) promoter of Escherichia coli in Pseudomonas putida. Construction of broad-host-range, controlled-expression vectorsGene, 1983
- Plasmid RP4 as a vector replicon in genetic engineeringNature, 1975
- Elimination by Ethidium Bromide of Antibiotic Resistance in Enterobacteria and StaphylococciJournal of General Microbiology, 1968