Multidrug-resistant Pseudomonas Aeruginosa Strain That Caused an Outbreak in a Neurosurgery Ward and Its Aac(6')-Iae Gene Cassette Encoding a Novel Aminoglycoside Acetyltransferase
Overview
Authors
Affiliations
We characterized multidrug-resistant Pseudomonas aeruginosa strains isolated from patients involved in an outbreak of catheter-associated urinary tract infections that occurred in a neurosurgery ward of a hospital in Sendai, Japan. Pulsed-field gel electrophoresis of SpeI-, XbaI-, or HpaI-digested genomic DNAs from the isolates revealed that clonal expansion of a P. aeruginosa strain designated IMCJ2.S1 had occurred in the ward. This strain possessed broad-spectrum resistance to aminoglycosides, beta-lactams, fluoroquinolones, tetracyclines, sulfonamides, and chlorhexidine. Strain IMCJ2.S1 showed a level of resistance to some kinds of disinfectants similar to that of a control strain of P. aeruginosa, ATCC 27853. IMCJ2.S1 contained a novel class 1 integron, In113, in the chromosome but not on a plasmid. In113 contains an array of three gene cassettes of bla(IMP-1), a novel aminoglycoside resistance gene, and the aadA1 gene. The aminoglycoside resistance gene, designated aac(6')-Iae, encoded a 183-amino-acid protein that shared 57.1% identity with AAC(6')-Iq. Recombinant AAC(6')-Iae protein showed aminoglycoside 6'-N-acetyltransferase activity by thin-layer chromatography. Escherichia coli expressing exogenous aac(6')-Iae showed resistance to amikacin, dibekacin, isepamicin, kanamycin, netilmicin, sisomicin, and tobramycin but not to arbekacin, gentamicins, or streptomycin. Alterations of gyrA and parC at the amino acid sequence level were detected in IMCJ2.S1, suggesting that such mutations confer the resistance to fluoroquinolones observed for this strain. These results indicate that P. aeruginosa IMCJ2.S1 has developed multidrug resistance by acquiring resistance determinants, including a novel member of the aac(6')-I family and mutations in drug resistance genes.
Martins J, da Silva E, Fernandes A, Costa de Oliveira S Bioengineering (Basel). 2024; 11(7).
PMID: 39061718 PMC: 11273671. DOI: 10.3390/bioengineering11070636.
Changes in the expression of mexB, mexY, and oprD in clinical Pseudomonas aeruginosa isolates.
Matsumoto Y, Yamasaki S, Hayama K, Iino R, Noji H, Yamaguchi A Proc Jpn Acad Ser B Phys Biol Sci. 2024; 100(1):57-67.
PMID: 38199247 PMC: 10864171. DOI: 10.2183/pjab.100.006.
Lee J, Kim N, Jang K, Jin H, Shin K, Jeong B Int J Mol Sci. 2023; 24(20).
PMID: 37894890 PMC: 10607276. DOI: 10.3390/ijms242015209.
Czobor Barbu I, Gheorghe-Barbu I, Grigore G, Vrancianu C, Chifiriuc M Int J Mol Sci. 2023; 24(9).
PMID: 37175597 PMC: 10178704. DOI: 10.3390/ijms24097892.
Khan F, Yaqoob S, Ali S, Tanveer N, Wang Y, Ashraf S Molecules. 2023; 28(1).
PMID: 36615406 PMC: 9822510. DOI: 10.3390/molecules28010212.