Characterization of CMY-type β-lactamases in clinical strains of Proteus mirabilis and Klebsiella pneumoniae isolated in four hospitals in the Paris area

被引:27
作者
Decré, D
Verdet, C
Raskine, L
Blanchard, H
Burghoffer, B
Philippon, A
Sanson-Le-Pors, MJ
Petit, JC
Arlet, G
机构
[1] Hop St Antoine, Serv Bacteriol, UFR St Antoine, F-75012 Paris, France
[2] Hop Lariboisiere, Serv Bacteriol, F-75475 Paris, France
[3] CHU Cochin, Serv Bacteriol, AP HP, Paris, France
[4] Hop Tenon, Serv Bacteriol, UFR St Antoine, F-75970 Paris, France
关键词
D O I
10.1093/jac/dkf193
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We isolated five clinical strains (three Proteus mirabilis and two Klebsiella pneumoniae) with beta-lactam resistance phenotypes consistent with production of an AmpC-type beta-lactamase. The predicted amino acid sequences of the enzymes were typical of class C beta-lactamases. The enzymes were identified as CMY-2, CMY-4 and a new CMY-variant beta-lactamase, CMY-12. The AmpC beta-lactamases from the two K. pneumoniae isolates were found to be encoded on self-transferable plasmids. The genes encoding the AmpC-type beta-lactamase produced by the three P. mirabilis isolates were chromosomal. Four of the five clinical isolates were from patients transferred from Greece, Algeria and Egypt; one of the K. pneumoniae strains was recovered from a French patient. PFGE analysis and rep-PCR fingerprinting showed that the two P. mirabilis isolates from Greek patients were closely related.
引用
收藏
页码:681 / 688
页数:8
相关论文
共 39 条
[21]   A plasmid-mediated CMY-2 beta-lactamase from an Algerian clinical isolate of Salmonella senftenberg [J].
Koeck, JL ;
Arlet, G ;
Philippon, A ;
Basmaciogullari, S ;
Thien, HV ;
Buisson, Y ;
Cavallo, JD .
FEMS MICROBIOLOGY LETTERS, 1997, 152 (02) :255-260
[22]   Transcontinental importation into the UK of Escherichia coli expressing a plasmid-mediated AmpC-type β-lactamase exposed during an outbreak of SHV-5 extended-spectrum β-lactamase in a Leeds hospital [J].
M'Zali, FH ;
Heritage, J ;
Gascoyne-Binzi, DM ;
Denton, M ;
Todd, NJ ;
Hawkey, PM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (06) :823-831
[23]   USE OF ANALYTICAL ISOELECTRIC FOCUSING FOR DETECTION AND IDENTIFICATION OF BETA-LACTAMASES [J].
MATTHEW, M ;
HARRIS, AM ;
MARSHALL, MJ ;
ROSS, GW .
JOURNAL OF GENERAL MICROBIOLOGY, 1975, 88 (MAY) :169-178
[24]   Outbreak of Klebsiella pneumoniae producing transferable AmpC-type β-lactamase (ACC-1) originating from Hafnia alvei [J].
Nadjar, D ;
Rouveau, M ;
Verdet, C ;
Donay, JL ;
Herrmann, JL ;
Lagrange, PH ;
Philippon, A ;
Arlet, G .
FEMS MICROBIOLOGY LETTERS, 2000, 187 (01) :35-40
[25]   CMY-2-producing Salmonella enterica, Klebsiella pneumoniae, Klebsiella oxytoca, Proteus mirabilis and Escherichia coli strains isolated in Spain (October 1999-December 2000) [J].
Navarro, F ;
Perez-Trallero, E ;
Marimon, JM ;
Aliaga, R ;
Gomariz, M ;
Mirelis, B .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 (03) :383-389
[26]   NOVEL PLASMID-MEDIATED BETA-LACTAMASE (MIR-1) CONFERRING RESISTANCE TO OXYIMINO-LACTAMS AND ALPHA-METHOXY BETA-LACTAMS IN CLINICAL ISOLATES OF KLEBSIELLA-PNEUMONIAE [J].
PAPANICOLAOU, GA ;
MEDEIROS, AA ;
JACOBY, GA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (11) :2200-2209
[27]   IMPROVED TOOLS FOR BIOLOGICAL SEQUENCE COMPARISON [J].
PEARSON, WR ;
LIPMAN, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2444-2448
[28]   Plasmid-determined AmpC-type β-lactamases [J].
Philippon, A ;
Arlet, G ;
Jacoby, GA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :1-11
[29]  
PHILIPPON A, 1994, EUR J CLIN MICROBIOL, V13, P17
[30]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467