Comparative activity of ertapenem against extended-spectrum beta lactamase-producing or plasmid-mediated AmpC beta lactamase-producing Klebsiella pneumoniae

被引:3
作者
Ramon Hernandez, Jose [1 ]
del Carmen Conejo, Maria [1 ]
Pascual, Alvaro [1 ,2 ]
机构
[1] Univ Seville, Fac Med, Dept Microbiol, Seville, Spain
[2] Hosp Univ Virgen Macarena, Dept Microbiol, Seville, Spain
来源
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA | 2010年 / 28卷 / 01期
关键词
Ertapenem; Extended-spectrum beta-lactamase; Plasmid AmpC; Porin; Inoculum effect; IN-VIVO DEVELOPMENT; ESCHERICHIA-COLI; CLINICAL ISOLATE; RESISTANCE; COMBINATION; GENES;
D O I
10.1016/j.eimc.2009.03.003
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: The effect of porin loss and inoculum size on the comparative activity of ertapenem against either extended-spectrum beta lactamase-producing (ESBL) or plasmid-mediated AmpC beta lactamase-producing (pACBL) Klebsiella pneumoniae strains was evaluated. Methods: Microdilution using 2 different bacterial inocula. Results: Imipenem, amikacin, ertapenem, and cefepime were the most active agents under standard conditions. Ertapenem was more highly affected by porin loss than imipenem. Conclusions: Ertapenem showed high activity against K. pneumoniae strains expressing ESBL, pACBL OF both. Strains deficient in porins showed decreased susceptibility to beta lactams. The inoculum effect had a greater impact on imipenem than on ertapenem. (C) 2008 Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:27 / 30
页数:4
相关论文
共 17 条
[11]   Porin expression in clinical isolates of Klebsiella pneumoniae [J].
Hernández-Allés, S ;
Albertí, S ;
Alvarez, D ;
Doménech-Sánchez, A ;
Martínez-Martínez, L ;
Gil, J ;
Tomás, JM ;
Benedí, VJ .
MICROBIOLOGY-UK, 1999, 145 :673-679
[12]   High-level carbapenem resistance in a Klebsiella pneumoniae clinical isolate is due to the combination of blaACT-1 β-lactamase production, porin OmpK35/36 insertional inactivation, and down-regulation of the phosphate transport porin PhoE [J].
Kaczmarek, Frank M. ;
Dib-Hajj, Fadia ;
Shang, Wenchi ;
Gootz, Thomas D. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (10) :3396-3406
[13]   Collateral damage of flomoxef therapy:: in vivo development of porin deficiency and acquisition of blaDHA-1 leading to ertapenem resistance in a clinical isolate of Klebsiella pneumoniae producing CTX-M-3 and SHV-5 β-lactamases [J].
Lee, Chen-Hsiang ;
Chu, Chishih ;
Liu, Jien-Wei ;
Chen, Yi-Shung ;
Chiu, Chiung-Jung ;
Su, Lin-Hui .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2007, 60 (02) :410-413
[14]   Roles of β-lactamases and porins is activities of carbapenems and cephalosporins against Klebsiella pneumoniae [J].
Martínez-Martínez, L ;
Pascual, A ;
Hernández-Allés, S ;
Alvarez-Díaz, D ;
Suárez, AI ;
Tran, SJ ;
Benedi, VJ ;
Jacoby, GA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (07) :1669-1673
[15]   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
[16]   Detection of plasmid-mediated AmpC β-lactamase genes in clinical isolates by using multiplex PCR [J].
Pérez-Pérez, FJ ;
Hanson, ND .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2153-2162
[17]   Cefepime, piperacillin-tazobactam, and the inoculum effect in tests with extended-spectrum β-lactamase-producing Enterobacteriaceae [J].
Thomson, KS ;
Moland, ES .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (12) :3548-3554