Susceptibility patterns to extended-spectrum cephalosporins among Enterobacteriaceae harbouring extended-spectrum β-lactamases using the updated Clinical and Laboratory Standards Institute interpretive criteria

被引:14
|
作者
Kristo, Ioulia [1 ]
Pitiriga, Vassiliki [2 ]
Poulou, Aggeliki [2 ,3 ]
Zarkotou, Olympia [4 ]
Kimouli, Maria [5 ]
Pournaras, Spyros [1 ]
Tsakris, Athanassios [2 ]
机构
[1] Univ Thessaly, Sch Med, Dept Microbiol, Larisa, Greece
[2] Univ Athens, Sch Med, Dept Microbiol, GR-11527 Athens, Greece
[3] Serres Gen Hosp, Dept Microbiol, Serres, Greece
[4] Tzane Gen Hosp, Dept Microbiol, Piraeus, Greece
[5] St Panteleimon Hosp, Dept Microbiol, Nicea, Greece
关键词
Extended-spectrum beta-lactamase; Extended-spectrum cephalosporins; CLSI breakpoints; ESCHERICHIA-COLI; KLEBSIELLA-PNEUMONIAE; INFECTIONS; ORGANISMS;
D O I
10.1016/j.ijantimicag.2012.12.003
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We examined the effect of applying the updated 2010 Clinical and Laboratory Standards Institute (CLSI) susceptibility breakpoints for extended-spectrum cephalosporins (ESCs) to detect extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae. In total, 202 ESBL-producing, plasmidic AmpC- and carbapenemase-negative isolates derived from separate patients were collected from three Greek hospitals during 2007-2011, including 150 Escherichia coli, 43 Klebsiella pneumoniae and 9 Enterobacter cloacae clinical isolates. ESBLs were detected using the ESBL CLSI confirmatory test and PCR assays. Sequencing analysis showed that 91 (45.0%) of the ESBL-producers carried the bla(CTX-M-3) gene, 66 (32.7%) carried the bla(CTX-M-15) gene and the remaining 45 (22.3%) carried the bla(SHV-5) gene. Minimum inhibitory concentrations for cefotaxime, ceftazidime and cefepime were determined by the agar dilution method. Based on the new CLSI breakpoints, 13 (6.4%) of the ESBL-producers were susceptible to cefotaxime, 90 (44.6%) to ceftazidime and 112 (55.4%) to cefepime; as many as 145 (71.8%) were susceptible to at least one ESC. Among the 150 E. coli, 12 (8.0%), 87 (58.0%) and 79 (52.7%) were susceptible to cefotaxime, ceftazidime and cefepime, respectively, whilst among the 43 K. pneumoniae, 1 (2.3%), 3 (7.0%) and 25 (58.1%) were susceptible to the above ESCs, respectively. None of the nine E. cloacae were susceptible to cefotaxime and ceftazidime, but all except one were susceptible to cefepime. By implementation of the new 2010 CLSI breakpoints, a considerable proportion of ESBL-possessing Enterobacteriaceae would be reported as susceptible, mostly to ceftazidime and cefepime, leading to possible infection control and therapeutic implications. (C) 2013 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:383 / 387
页数:5
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