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LY127935的体外活性。

In vitro activity of LY127935.

作者信息

Fass R J

出版信息

Antimicrob Agents Chemother. 1979 Oct;16(4):503-9. doi: 10.1128/AAC.16.4.503.

Abstract

LY127935 is a unique new beta-lactam antibiotic. Its activity against 536 clinical isolates was studied by using microdilution methods of susceptibility testing and compared with the activities of cefamandole, cefoxitin, and cephalothin. The lowest concentrations required to inhibit at least 90% of strains tested (MIC(90)s) of LY127935 for Staphylococcus aureus, Streptococcus pyogenes, Streptococcus agalactiae, and Streptococcus pneumoniae ranged from 2 to 8 mug/ml. The MIC(90)s for other staphylococci and streptococci were higher. The MIC(90)s for Enterobacteriaceae and Pseudomonas species ranged from 0.12 to 8 mug/ml and 8 to >32 mug/ml, respectively. The MIC(90)s for anaerobes ranged from 2 to >32 mug/ml. As determined by MIC(90)s, LY127935 was consistently the least active antibiotic against facultatively anaerobic gram-positive cocci and the most active against aerobic and facultatively anaerobic gram-negative bacilli. Its position with respect to activity against anaerobes varied from being the most active against Bacteroides fragilis and Clostridium perfringens to the least active against anaerobic cocci. In a population of multidrug-resistant isolates, concentrations of 8 mug or less of LY127935 per ml inhibited 82% of Enterobacteriaceae; concentrations of 32 mug or less per ml inhibited 100% of Enterobacteriaceae and 40% of P. aeruginosa. Increasing the inoculum size by 100-fold did not increase the minimal inhibitory concentrations of LY127935 or cefoxitin but did increase minimal inhibitory concentrations of cefamandole and cephalothin for some Enterobacteriaceae. All four drugs were bactericidal; minimal bactericidal concentrations were the same or one concentration higher than minimal inhibitory concentrations for 91 to 96% of strains tested. The broad spectrum and marked in vitro activity of LY127935 make it a promising new antibiotic.

摘要

LY127935是一种独特的新型β-内酰胺抗生素。采用微量稀释法药敏试验研究了其对536株临床分离菌的活性,并与头孢孟多、头孢西丁和头孢噻吩的活性进行了比较。LY127935对金黄色葡萄球菌、化脓性链球菌、无乳链球菌和肺炎链球菌抑制至少90%受试菌株所需的最低浓度(MIC90s)为2至8μg/ml。其他葡萄球菌和链球菌的MIC90s较高。肠杆菌科细菌和假单胞菌属的MIC90s分别为0.12至8μg/ml和8至>32μg/ml。厌氧菌的MIC90s为2至>32μg/ml。根据MIC90s测定,LY127935始终是对兼性厌氧革兰氏阳性球菌活性最低的抗生素,而对需氧和兼性厌氧革兰氏阴性杆菌活性最高。其对厌氧菌的活性地位有所不同,对脆弱拟杆菌和产气荚膜梭菌活性最高,而对厌氧球菌活性最低。在多药耐药分离菌群体中,每毫升8μg或更低浓度的LY127935可抑制82%的肠杆菌科细菌;每毫升32μg或更低浓度可抑制100%的肠杆菌科细菌和40%的铜绿假单胞菌。将接种量增加100倍不会增加LY127935或头孢西丁的最低抑菌浓度,但会增加某些肠杆菌科细菌对头孢孟多和头孢噻吩的最低抑菌浓度。所有四种药物均具有杀菌作用;91%至96%受试菌株的最低杀菌浓度与最低抑菌浓度相同或高一个浓度。LY127935的广谱和显著体外活性使其成为一种有前景的新型抗生素。

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