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新型青霉烯类药物FCE 22101和FCE 24362单独或与氨基糖苷类药物联合应用对从心内膜炎患者分离出的链球菌的体外活性。

In-vitro activity of the new penems FCE 22101 and FCE 24362 alone or in combination with aminoglycosides against streptococci isolated from patients with endocarditis.

作者信息

Dornbusch K, Henning C, Lindén E

机构信息

Department of Clinical Bacteriology, Sundsvall Hospital, Sweden.

出版信息

J Antimicrob Chemother. 1989 Mar;23 Suppl C:109-17. doi: 10.1093/jac/23.suppl_c.109.

Abstract

Seven strains of viridans streptococci isolated from patients with endocarditis were inhibited in vitro by 0.06-2 mg/l and 0.016-0.5 mg/l of the penems FCE 22101 and FCE 24362 respectively. The MBCs were the same or two-fold higher than the respective MIC with three exceptions. One strain of Streptococcus faecalis was only inhibited (8 mg/ml respectively 0.5 mg/l; MBC greater than 32 mg/l) and one strain of Str. faecium was resistant (MIC greater than or equal to 16 mg/l). When combined with gentamicin or netilmicin a bactericidal and synergistic killing was observed within 1-8 h in all strains except Str. faecium. Synergy could also be confirmed in all cases by following bacterial growth kinetics after elimination of antibiotics, by calculating the difference between the times required for bacteria exposed to antibiotic and unexposed bacteria to increase in numbers (PAE).

摘要

从心内膜炎患者中分离出的七株草绿色链球菌在体外分别被0.06 - 2毫克/升和0.016 - 0.5毫克/升的青霉烯类药物FCE 22101和FCE 24362抑制。除三个例外情况外,最低杀菌浓度(MBC)与各自的最低抑菌浓度(MIC)相同或高两倍。一株粪肠球菌仅被抑制(分别为8毫克/毫升和0.5毫克/升;MBC大于32毫克/升),一株屎肠球菌耐药(MIC大于或等于16毫克/升)。除屎肠球菌外,在所有菌株中,当与庆大霉素或奈替米星联合使用时,在1 - 8小时内观察到杀菌和协同杀灭作用。在所有情况下,通过在去除抗生素后跟踪细菌生长动力学,计算暴露于抗生素的细菌和未暴露细菌数量增加所需时间之间的差异(PAE),也可以证实协同作用。

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