ANTIBACTERIAL IN-VITRO ACTIVITY OF PIPERACILLIN-TAZOBACTAM IN COMBINATION WITH NETILMICIN OR AMIKACIN AGAINST AMOXICILLIN-RESISTANT STRAINS OF ENTEROBACTERIACEAE

被引:0
作者
DUEZ, JM
SIEBOR, E
PECHINOT, A
CORDIN, X
CHAMARDNEUWIRTH, C
KAZMIERCZAK, A
机构
来源
PATHOLOGIE BIOLOGIE | 1995年 / 43卷 / 03期
关键词
IN VITRO ACTIVITY; PIPERACILLIN TAZOBACTAM; AMINOGLYCOSIDE; ANTIBIOTIC COMBINATION; ENTEROBACTERIACEAE;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The antibacterial in vitro activity of piperacillin and tazobactam (in a concentration ratio of 8/1) was studied in combination with netilmicin or amikacin by a microtiter checkerboard assay against 162 strains of Enterobacteriaceae. These strains were selected for their resistance pattern to beta-lactam antibiotics and their beta-lactamases were characterized by the mean of isoelectric focusing in comparison with reference strains. A comparison of the MICs of piperacillin, alone and in combination, assessed the efficacy of tazobactam as beta-lactamase inhibitor, particularly when a TEM-1 beta-lactamase was produced. When the strains were sensitive to the aminoglycosides(lll netilmicin-sensitive ones and 131 amikacin-sensitive ones), we observed 55 % of synergistic effects and 45 % of additions with the combinations piperacillin-tazobactam-netilmicin or amikacin. A synergistic effect was usually encountered with P. mirabilis, P. vulgaris, M, morganii and with the strains off. coli, E. cloacae and S. marcescens which produced a cephalosporinase only. Among the 51 strains that were intermediate or resistant to netilmicin, 8 ones were inhibited by piperacillin-tazobactam-netilmicin at therapeutic levels (3 synergisms, 5 additions). Among the 31 strains that were intermediate or resistant to amikacin, 24 ones (18 synergisms, 6 additions) were inhibited by piperacillin-tazobactam-amikacin at therapeutic concentrations. In most of the cases, the combination of piperacillin-tazobactam with an aminoglycoside enhanced the antibacterial activity of these agents by decreasing the concentrations necessary to inhibit the strains.
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页码:208 / 214
页数:7
相关论文
共 19 条
[1]  
Acar J., 1992, Pathologie Biologie, V40, P741
[2]   SUSCEPTIBILITY SURVEY OF PIPERACILLIN ALONE AND IN THE PRESENCE OF TAZOBACTAM [J].
ACAR, JF ;
GOLDSTEIN, FW ;
KITZIS, MD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 :23-28
[3]   BETA-LACTAMASES - DETERMINATION OF THEIR ISOELECTRIC POINTS [J].
BARTHELEMY, M ;
GUIONIE, M ;
LABIA, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1978, 13 (04) :695-698
[4]  
CHANAL M, 1986, PRESSE MED, V15, P2313
[5]  
COOKSEY R, 1990, ANTIMICROB AGENTS CH, V34, P734
[6]  
DUEZ JM, 1991, PATHOL BIOL, V39, P374
[7]   COMPARATIVE-EVALUATION OF A NEW BETA-LACTAMASE INHIBITOR, YTR 830, COMBINED WITH DIFFERENT BETA-LACTAM ANTIBIOTICS AGAINST BACTERIA HARBORING KNOWN BETA-LACTAMASES [J].
GUTMANN, L ;
KITZIS, MD ;
YAMABE, S ;
ACAR, JF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 29 (05) :955-957
[8]   ACTIVITIES OF BETA-LACTAM ANTIBIOTICS AGAINST ESCHERICHIA-COLI STRAINS PRODUCING EXTENDED-SPECTRUM BETA-LACTAMASES [J].
JACOBY, GA ;
CARRERAS, I .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (05) :858-862
[9]   DISSEMINATION OF THE NOVEL PLASMID-MEDIATED BETA-LACTAMASE CTX-1, WHICH CONFERS RESISTANCE TO BROAD-SPECTRUM CEPHALOSPORINS, AND ITS INHIBITION BY BETA-LACTAMASE INHIBITORS [J].
KITZIS, MD ;
BILLOTKLEIN, D ;
GOLDSTEIN, FW ;
WILLIAMSON, R ;
NHIEU, GTV ;
CARLET, J ;
ACAR, JF ;
GUTMANN, L .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (01) :9-14
[10]   COMPARATIVE INVITRO AND INVIVO ACTIVITIES OF PIPERACILLIN COMBINED WITH THE BETA-LACTAMASE INHIBITORS TAZOBACTAM, CLAVULANIC ACID, AND SULBACTAM [J].
KUCK, NA ;
JACOBUS, NV ;
PETERSEN, PJ ;
WEISS, WJ ;
TESTA, RT .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (11) :1964-1969