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肽脱甲酰基酶抑制剂对革兰氏阳性病原体的体外活性

In vitro activities of peptide deformylase inhibitors against gram-positive pathogens.

作者信息

Wise R, Andrews J M, Ashby J

机构信息

Department of Microbiology, City Hospital NHS Trust, Birmingham, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2002 Apr;46(4):1117-8. doi: 10.1128/AAC.46.4.1117-1118.2002.

Abstract

The activities of six peptide deformylase (PDF) inhibitors against 107 respiratory tract pathogens were studied and compared to those of ciprofloxacin and amoxicillin-clavulanate. Against Streptococcus pneumoniae, BB-83698 and BB-83815 were the most active PDF inhibitors (MIC at which 90% of the organisms tested were inhibited [MIC(90)], 0.25 microg/ml). Five of the agents showed similar activity against Moraxella catarrhalis (MIC(90), 0.12 microg/ml). All PDF inhibitors were less active against Haemophilus influenzae; BB-3497 was the most active agent (MIC(90), 2 microg/ml). Five agents were studied against Chlamydia spp. and showed activity similar to that of ciprofloxacin (MIC, 0.5 to 4 microg/ml). This study demonstrates that PDF inhibitors have the potential to be developed for the treatment of respiratory tract infections.

摘要

研究了六种肽脱甲酰基酶(PDF)抑制剂对107种呼吸道病原体的活性,并与环丙沙星和阿莫西林-克拉维酸进行了比较。针对肺炎链球菌,BB-83698和BB-83815是活性最强的PDF抑制剂(使90%受试菌株受到抑制的最低抑菌浓度[MIC(90)]为0.25微克/毫升)。其中五种药物对卡他莫拉菌显示出相似的活性(MIC(90)为0.12微克/毫升)。所有PDF抑制剂对流感嗜血杆菌的活性较低;BB-3497是活性最强的药物(MIC(90)为2微克/毫升)。研究了五种药物对衣原体属的作用,其活性与环丙沙星相似(MIC为0.5至4微克/毫升)。该研究表明,PDF抑制剂有开发用于治疗呼吸道感染的潜力。

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