Tazobactam is a potent inactivator of selected inhibitor-resistant class A beta-lactamases

被引:37
作者
Bonomo, RA [1 ]
Rudin, SA [1 ]
Shlaes, DM [1 ]
机构
[1] CASE WESTERN RESERVE UNIV,UNIV HOSP CLEVELAND,GERIATR CARE CTR,DEPT MED,CLEVELAND,OH 44120
关键词
inhibitor-resistant beta-lactamase; piperacillin; tazobactam; ESCHERICHIA-COLI; SULBACTAM; MUTATIONS;
D O I
10.1016/S0378-1097(97)00013-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The beta-lactam beta-lactamase inhibitor combinations (ampicillin/clavulanate, ampicillin/sulbactam, ticarcillin/clavulanate and piperacillin/tazobactam) were tested against selected inhibitor-resistant class A beta-lactamases of the TEM and OHIO-1 varieties. Minimum inhibitor concentrations (MIC) revealed that the Escherichia coli DH5 alpha transconjugate strains that possessed the OHIO-1 beta-lactamase, Met(69)Ile mutant of the OHIO-1 beta-lactamase, TEM-30 (Arg(244)Ser) and TEM-31 (Arg(244)Cys) beta-lactamase were most susceptible to piperacillin and piperacillin/tazobactam. Kinetic experiments with each beta-lactamase demonstrated that tazobactam was 10-25-fold more potent than clavulanate or sulbactam against TEM-30 and TEM-31 beta-lactamase. Tazobactam was also as effective as clavulanate against the Met(69)Ile mutant of the OHIO-1 beta-lactamase. Among the clinically available beta-lactams and beta-lactamase inhibitors, piperacillin/tazobactam appears to be the most potent combination against selected inhibitor-resistant strains of TEM and OHIO-1 beta-lactamase.
引用
收藏
页码:59 / 62
页数:4
相关论文
共 13 条
  • [1] A STANDARD NUMBERING SCHEME FOR THE CLASS-A BETA-LACTAMASES
    AMBLER, RP
    COULSON, AFW
    FRERE, JM
    GHUYSEN, JM
    JORIS, B
    FORSMAN, M
    LEVESQUE, RC
    TIRABY, G
    WALEY, SG
    [J]. BIOCHEMICAL JOURNAL, 1991, 276 : 269 - 270
  • [2] BELAAOUAJ A, 1994, FEMS MICROBIOL LETT, V120, P75
  • [3] CHARACTERIZATION OF A NEW TEM-TYPE BETA-LACTAMASE RESISTANT TO CLAVULANATE, SULBACTAM, AND TAZOBACTAM IN A CLINICAL ISOLATE OF ESCHERICHIA-COLI
    BLAZQUEZ, J
    BAQUERO, MR
    CANTON, R
    ALOS, I
    BAQUERO, F
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (10) : 2059 - 2063
  • [4] BETA-LACTAMASE MUTATIONS FAR FROM THE ACTIVE-SITE INFLUENCE INHIBITOR BINDING
    BONOMO, RA
    DAWES, CG
    KNOX, JR
    SHLAES, DM
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1995, 1247 (01): : 121 - 125
  • [5] OHIO-1 BETA-LACTAMASE RESISTANT TO MECHANISM-BASED INACTIVATORS
    BONOMO, RA
    CURRIEMCCUMBER, C
    SHLAES, DM
    [J]. FEMS MICROBIOLOGY LETTERS, 1992, 92 (01) : 79 - 82
  • [6] COMPLEMENTARY ROLES OF MUTATIONS AT POSITION-69 AND POSITION-242 IN A CLASS-A BETA-LACTAMASE
    BONOMO, RA
    DAWES, CG
    KNOX, JR
    SHLAES, DM
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1995, 1247 (01): : 113 - 120
  • [7] Implication of Ile-69 and Thr-182 residues in kinetic characteristics of IRT-3 (TEM-32) beta-lactamase
    Farzaneh, S
    Chaibi, EB
    Peduzzi, J
    Barthelemy, M
    Labia, R
    Blazquez, J
    Baquero, F
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (10) : 2434 - 2436
  • [8] MOLECULAR CHARACTERIZATION OF 9 DIFFERENT TYPES OF MUTANTS AMONG 107 INHIBITOR-RESISTANT TEM BETA-LACTAMASES FROM CLINICAL ISOLATES OF ESCHERICHIA-COLI
    HENQUELL, C
    CHANAL, C
    SIROT, D
    LABIA, R
    SIROT, J
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (02) : 427 - 430
  • [9] DETERMINANTS OF THE ACTIVITY OF BETA-LACTAMASE INHIBITOR COMBINATIONS
    LIVERMORE, DM
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 : 9 - 21
  • [10] COMPARATIVE ACTIVITIES OF CLAVULANIC ACID, SULBACTAM, AND TAZOBACTAM AGAINST CLINICALLY IMPORTANT BETA-LACTAMASES
    PAYNE, DJ
    CRAMP, R
    WINSTANLEY, DJ
    KNOWLES, DJC
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (04) : 767 - 772