Tausk F, Stratton C W
Antimicrob Agents Chemother. 1986 Oct;30(4):584-9. doi: 10.1128/AAC.30.4.584.
We studied the ability of clavulanic acid (CA) to induce beta-lactamase in Pseudomonas aeruginosa isolates and what effect this might have on the susceptibilities to beta-lactam agents. We first used a disk approximation method to test 4 laboratory and 16 clinical P. aeruginosa isolates against antipseudomonal beta-lactam agents for truncation by CA and found this to be very common. All antimicrobial compounds except imipenem demonstrated truncation in the vicinity of CA. We also evaluated the extent to which chromosomal beta-lactamase is induced by CA and found this to occur to some degree in most isolates and to be dependent on the concentration of CA. Finally, we performed time kill curves on these isolates to compare bacterial growth in ticarcillin alone with growth in ticarcillin-CA (the CA at 2 or 4 micrograms/ml). We found that CA at this concentration has neither an antagonistic nor a synergistic antibacterial effect in combination with ticarcillin.
我们研究了克拉维酸(CA)诱导铜绿假单胞菌分离株产生β-内酰胺酶的能力,以及这可能对β-内酰胺类药物敏感性产生的影响。我们首先使用纸片扩散法,针对4株实验室分离株和16株临床分离的铜绿假单胞菌,检测其对抗假单胞菌β-内酰胺类药物被CA截断的情况,发现这非常常见。除亚胺培南外,所有抗菌化合物在CA附近均表现出截断现象。我们还评估了CA诱导染色体β-内酰胺酶的程度,发现大多数分离株在一定程度上会出现这种情况,且这取决于CA的浓度。最后,我们对这些分离株进行了时间杀菌曲线实验,以比较单独使用替卡西林时的细菌生长情况与替卡西林 - CA(CA浓度为2或4微克/毫升)组合时的细菌生长情况。我们发现,该浓度的CA与替卡西林联合使用时既无拮抗作用也无协同抗菌作用。