Dornbusch K, Nord C E, Olsson-Liljeqvist B
Scand J Infect Dis Suppl. 1979(19):17-25.
It was shown that recent Swedish clinical isolates of anaerobic bacteria are susceptible to many antibiotics by the agar dilution method with the exception of the Bacteroides group versus beta-lactam antibiotics or tetracyclines. Strains of B. fragilis were inhibited by 4--greater than 128 micrograms benzylpenicillin or cephalothin/ml, 1.0--64 micrograms cefoxitin/ml, 0.064--2 micrograms clindamycin or metronidazole/ml, 2--8 micrograms chloramphenicol/ml, 2--16 micrograms fusidic acid/ml and 0.032--32 micrograms doxycycline/ml. Resistance to beta-lactam antibiotics was partly due to the production of beta-lactamase. Growth of beta-lactamase producing strains in the presence of enzyme inhibitors such as clavulanic acid or CP-45899 together with cephaloridine lowered the MIC's manyfold. Cefoxitin with relative resistance to beta-lactamases inhibited the majority of the strains at 8 micrograms/ml. Cefoxitin-resistant strains (MIC greater than or equal to 16 micrograms/ml) were also resistant to the new cephalosporins BL-S786 and HR-756 as well as to the new cefamycins A, B, CL619-183, CS-1170 and Sq-14359 and to thienamycin. Cefamycin CL619-183, only showed a slightly higher in vitro activity than cefoxitin. Resistance to the cefamycins could not be correlated to the production of beta-lactamases.
结果表明,除类杆菌属对β-内酰胺类抗生素或四环素外,近期瑞典临床分离的厌氧菌通过琼脂稀释法对许多抗生素敏感。脆弱拟杆菌菌株对4~大于128μg/ml苄青霉素或头孢噻吩、1.0~64μg/ml头孢西丁、0.064~2μg/ml克林霉素或甲硝唑、2~8μg/ml氯霉素、2~16μg/ml夫西地酸和0.032~32μg/ml强力霉素敏感。对β-内酰胺类抗生素的耐药性部分归因于β-内酰胺酶的产生。在存在酶抑制剂如克拉维酸或CP-45899以及头孢菌素的情况下,产β-内酰胺酶菌株的生长使最低抑菌浓度降低了许多倍。对β-内酰胺酶相对耐药的头孢西丁在8μg/ml时可抑制大多数菌株。耐头孢西丁菌株(最低抑菌浓度大于或等于16μg/ml)对新头孢菌素BL-S786和HR-756以及新头孢霉素A、B、CL619-183、CS-1170和Sq-14359以及噻烯霉素也耐药。头孢霉素CL619-183的体外活性仅略高于头孢西丁。对头孢霉素的耐药性与β-内酰胺酶的产生无关。