DISTRIBUTION AND CHARACTERIZATION OF BETA-LACTAMASES OF MYCOBACTERIA AND RELATED ORGANISMS

被引:46
作者
KWON, HH
TOMIOKA, H
SAITO, H
机构
[1] Department of Microbiology and Immunology, Shimane Medical University, Izumo
来源
TUBERCLE AND LUNG DISEASE | 1995年 / 76卷 / 02期
关键词
D O I
10.1016/0962-8479(95)90557-X
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Setting: The detailed distribution and precise features of mycobacterial beta-lactamases urgently need to be elucidated. Objective: To study the distribution pattern of beta-lactamases among mycobacteria, their enzymatic profiles and degree of contribution to the expression of drug resistance of some mycobacteria to beta-lactam antibiotics. Design: Cell-associated beta-lactamase was measured by nitrocefin disc method. beta-lactamases obtained from some mycobacteria were studied for their substrate specificity, metal ion-dependency and isoelectric focusing (IEF) patterns. Changes in the minimum inhibitory concentrations (MICs) of beta-lactams for rapidly growing mycobacteria due to the combined use of tazobactam were measured. Results: In slow growers, Mycobacterium tuberculosis complex possessed strong and M. kansasii showed strong to intermediate beta-lactamase activity, while M. avium complex lacked such an activity. All the rapid growers possessed strong to intermediate activity. The beta-lactamases of test organisms including M. tuberculosis, M. kansasii, M. fortuitum etc, exerted both penicillinase and cephalosporinase activities and were not metallo-enzymes. M. tuberculosis, M. kansasii, and M. smegmatis exhibited the species-specific IEF patterns of beta-lactamases. Tazobactam potentiated the in vitro antimicrobial activities of some beta-lactams against M. fortuitum and M. chelonae. Conclusion: Many mycobacteria possessed peculiar beta-lactamases and the enzymes were partly attributable to their drug resistance to certain beta-lactam antibiotics.
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页码:141 / 148
页数:8
相关论文
共 35 条
[1]   CHARACTERIZATION OF A BETA-LACTAMASE PRODUCED IN MYCOBACTERIUM-FORTUITUM D316 [J].
AMICOSANTE, G ;
FRANCESCHINI, N ;
SEGATORE, B ;
ORATORE, A ;
FATTORINI, L ;
OREFICI, G ;
VANBEEUMEN, J ;
FRERE, JM .
BIOCHEMICAL JOURNAL, 1990, 271 (03) :729-734
[2]   NEW TEST METHOD FOR DEMONSTRATING B-LACTAMASE ACTIVITY AMONG MYCOBACTERIA AND NOCARDIA [J].
BACKELIN, B ;
LIND, A ;
RIDELL, M .
TUBERCLE, 1973, 54 (04) :297-307
[3]  
BONICKE R, 1957, Zentralbl Bakteriol Orig, V170, P366
[5]   CHARACTERIZATION OF BETA-LACTAMASES [J].
BUSH, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (03) :259-263
[7]  
BUSH K, 1988, REV INFECT DIS, V10, P681
[8]  
CHOUBEY D, 1986, BIOCHEM INT, V12, P207
[9]  
DUFOUR AP, 1966, AM REV RESPIR DIS, V94, P965
[10]   BETA-LACTAMASE OF MYCOBACTERIUM-FORTUITUM - KINETICS OF PRODUCTION AND RELATIONSHIP WITH RESISTANCE TO BETA-LACTAM ANTIBIOTICS [J].
FATTORINI, L ;
SCARDACI, G ;
JIN, SH ;
AMICOSANTE, G ;
FRANCESCHINI, N ;
ORATORE, A ;
OREFICI, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (09) :1760-1764