Sanders C C, Sanders W E, Goering R V
Antimicrob Agents Chemother. 1982 Jun;21(6):968-75. doi: 10.1128/AAC.21.6.968.
We assessed the extent and mechanisms of antagonism of beta-lactam antibiotics by cefoxitin. In tests with 41 gram-negative isolates, cefoxitin antagonized cephalothin, cefamandole, cefsulodin, cefotaxime, moxalactam, ampicillin, carbenicillin, piperacillin, mezlocillin, and azlocillin, but not cephalexin, mecillinam, or N-formimidoyl thienamycin. The extent of antagonism varied with the beta-lactam and genus studied. However, antagonism occurred most often with strains possessing inducible cephalosporinases. Antagonism of cephalothin and cefamandole correlated closely with the induction of beta-lactamases capable of inactivating these drugs. Although antagonism of the remaining drugs occurred more often with strains possessing inducible beta-lactamases, these enzymes did not inactivate the drugs. Morphological studies revealed that cefoxitin inhibited filamentation and lysis produced by various beta-lactam drugs. Results of this investigation suggest that cefoxitin antagonizes beta-lactams via (i) induction of drug-inactivating beta-lactamases, and (ii) the induction of beta-lactamases that cannot inactivate the drug but serve as barriers against access to target proteins. This barrier appears most efficient for drugs that bind to penicillin-binding proteins 1 and 3.
我们评估了头孢西丁对β-内酰胺类抗生素的拮抗程度及机制。在用41株革兰氏阴性菌进行的试验中,头孢西丁拮抗头孢噻吩、头孢孟多、头孢磺啶、头孢噻肟、拉氧头孢、氨苄西林、羧苄西林、哌拉西林、美洛西林和阿洛西林,但不拮抗头孢氨苄、美西林或N-甲酰亚胺硫霉素。拮抗程度因所研究的β-内酰胺类药物和菌属而异。然而,拮抗作用最常发生在具有诱导型头孢菌素酶的菌株中。头孢噻吩和头孢孟多的拮抗作用与能够使这些药物失活的β-内酰胺酶的诱导密切相关。虽然其余药物的拮抗作用在具有诱导型β-内酰胺酶的菌株中更常发生,但这些酶并未使药物失活。形态学研究表明,头孢西丁抑制了各种β-内酰胺类药物产生的丝状化和裂解。本研究结果表明,头孢西丁通过以下方式拮抗β-内酰胺类药物:(i)诱导使药物失活的β-内酰胺酶,以及(ii)诱导不能使药物失活但可作为阻止药物接近靶蛋白屏障的β-内酰胺酶。对于与青霉素结合蛋白1和3结合的药物,这种屏障似乎最为有效。