Phenotypic Screening of Carbapenemases and Associated β-Lactamases in Carbapenem-Resistant Enterobacteriaceae

被引:96
作者
Birgy, Andre [1 ]
Bidet, Philippe [1 ,2 ]
Genel, Nathalie [3 ]
Doit, Catherine [1 ,2 ]
Decre, Dominique [3 ,4 ]
Arlet, Guillaume [3 ,5 ]
Bingen, Edouard [1 ,2 ]
机构
[1] Hop Robert Debre, AP HP, Microbiol Lab, F-75019 Paris, France
[2] Univ Paris Diderot, EA3105, Paris, France
[3] Univ Paris 06, Bacteriol Lab, Fac Med, ER8, Paris, France
[4] Hop St Antoine, AP HP, Bacteriol Lab, F-75571 Paris, France
[5] Hop Tenon, AP HP, Serv Bacteriol Hyg, F-75970 Paris, France
关键词
MODIFIED HODGE TEST; KLEBSIELLA-PNEUMONIAE; ESCHERICHIA-COLI; AMPC; DIVERSITY; EMERGENCE; INFECTION; ERTAPENEM; BACTERIA; SPREAD;
D O I
10.1128/JCM.06131-11
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Dissemination of carbapenem resistance among Enterobacteriaceae poses a considerable threat to public health. Carbapenemase gene detection by molecular methods is the gold standard but is available in only a few laboratories. The aim of this study was to test phenotypic methods for the detection of metallo-beta-lactamase (MBL)- or Klebsiella pneumoniae carbapenemase (KPC)-producing Enterobacteriaceae and associated mechanisms of beta-lactam resistance against a panel of 30 genotypically characterized carbapenem-resistant Enterobacteriaceae : 9 MBL, 7 KPC, 6 OXA-48, and 8 extended-spectrum beta-lactamase (ESBL) or AmpC beta-lactamases associated with decreased permeability. We used carbapenemase inhibitor-impregnated agar to test for carbapenem-resistant strains. Differences in the inhibition zone sizes of the meropenem, imipenem, ertapenem, and doripenem disks were measured between control and inhibitor (EDTA or phenylboronic acid [PBA] with or without cloxacillin)-impregnated Mueller-Hinton agar with a cutoff of 10 mm. All 9 MBL- and 7 KPC-producing Enterobacteriaceae were identified from the differences in zone size in the presence and absence of specific inhibitors, regardless of the carbapenem MICs and including isolates with low-level resistance to carbapenems. We also detected their associated beta-lactam resistance mechanisms (11 ESBL-type and 5 class A beta-lactamase 2b). No differences in zone size were observed for OXA-48-producing strains or other carbapenem resistance mechanisms such as ESBL and decreased permeability. We propose a new strategy to detect carbapenemases (MBL-and KPC-type) and associated mechanisms of beta-lactam resistance (ESBL or class A beta-lactamase 2b) by the use of inhibitor-impregnated agar. A rapid phenotypic detection of resistance mechanisms is important for epidemiological purposes and for limiting the spread of resistant strains by implementing specific infection control measures.
引用
收藏
页码:1295 / 1302
页数:8
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