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Characterization of a new metallo-beta-lactamase gene, bla(NDM-1), and a novel erythromycin esterase gene carried on a unique genetic structure in Klebsiella pneumoniae sequence type 14 from India.
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2009 Dec; Vol. 53 (12), pp. 5046-54. Date of Electronic Publication: 2009 Sep 21. - Publication Year :
- 2009
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Abstract
- A Swedish patient of Indian origin traveled to New Delhi, India, and acquired a urinary tract infection caused by a carbapenem-resistant Klebsiella pneumoniae strain that typed to the sequence type 14 complex. The isolate, Klebsiella pneumoniae 05-506, was shown to possess a metallo-beta-lactamase (MBL) but was negative for previously known MBL genes. Gene libraries and amplification of class 1 integrons revealed three resistance-conferring regions; the first contained bla(CMY-4) flanked by ISEcP1 and blc. The second region of 4.8 kb contained a complex class 1 integron with the gene cassettes arr-2, a new erythromycin esterase gene; ereC; aadA1; and cmlA7. An intact ISCR1 element was shown to be downstream from the qac/sul genes. The third region consisted of a new MBL gene, designated bla(NDM-1), flanked on one side by K. pneumoniae DNA and a truncated IS26 element on its other side. The last two regions lie adjacent to one another, and all three regions are found on a 180-kb region that is easily transferable to recipient strains and that confers resistance to all antibiotics except fluoroquinolones and colistin. NDM-1 shares very little identity with other MBLs, with the most similar MBLs being VIM-1/VIM-2, with which it has only 32.4% identity. As well as possessing unique residues near the active site, NDM-1 also has an additional insert between positions 162 and 166 not present in other MBLs. NDM-1 has a molecular mass of 28 kDa, is monomeric, and can hydrolyze all beta-lactams except aztreonam. Compared to VIM-2, NDM-1 displays tighter binding to most cephalosporins, in particular, cefuroxime, cefotaxime, and cephalothin (cefalotin), and also to the penicillins. NDM-1 does not bind to the carbapenems as tightly as IMP-1 or VIM-2 and turns over the carbapenems at a rate similar to that of VIM-2. In addition to K. pneumoniae 05-506, bla(NDM-1) was found on a 140-kb plasmid in an Escherichia coli strain isolated from the patient's feces, inferring the possibility of in vivo conjugation. The broad resistance carried on these plasmids is a further worrying development for India, which already has high levels of antibiotic resistance.
- Subjects :
- Amino Acid Sequence
Anti-Bacterial Agents metabolism
Anti-Bacterial Agents pharmacology
Carboxylic Ester Hydrolases classification
Cefotaxime metabolism
Cefotaxime pharmacology
Cefuroxime metabolism
Cefuroxime pharmacology
Cephalosporins metabolism
Cephalosporins pharmacology
Cephalothin metabolism
Cephalothin pharmacology
Drug Resistance, Multiple, Bacterial genetics
Drug Resistance, Multiple, Bacterial physiology
Electrophoresis, Gel, Pulsed-Field
Humans
India
Kinetics
Klebsiella pneumoniae drug effects
Microbial Sensitivity Tests
Molecular Sequence Data
Penicillins metabolism
Penicillins pharmacology
Sequence Analysis, DNA
Sequence Homology, Amino Acid
beta-Lactamases classification
Carboxylic Ester Hydrolases chemistry
Carboxylic Ester Hydrolases genetics
Klebsiella Infections microbiology
Klebsiella pneumoniae enzymology
Klebsiella pneumoniae genetics
beta-Lactamases chemistry
beta-Lactamases genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1098-6596
- Volume :
- 53
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 19770275
- Full Text :
- https://doi.org/10.1128/AAC.00774-09