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左氧氟沙星及其他三种氟喹诺酮类药物对青霉素敏感和耐药肺炎链球菌的体外抑菌活性

In-vitro bacteriostatic activity of levofloxacin and three other fluoroquinolones against penicillin-susceptible and penicillin-resistant Streptococcus pneumoniae.

作者信息

Frémaux A, Sissia G, Geslin P

机构信息

Service de Microbiologie, Centre Hospitalier Intercommunal Créteil, France.

出版信息

J Antimicrob Chemother. 1999 Jun;43 Suppl C:9-14. doi: 10.1093/jac/43.suppl_3.9.

Abstract

The purpose of this study was to investigate the in-vitro bacteriostatic activity of levofloxacin in comparison with that of ofloxacin, sparfloxacin and ciprofloxacin against 205 strains of Streptococcus pneumoniae (101 penicillin-susceptible, 51 penicillin-intermediate and 53 penicillin-resistant). The isolates were provided between September 1996 and October 1996 by French hospitals participating in the National Co-operative Survey of Pneumococcal Infections. The determination of MICs (mg/L) was made by the agar dilution method. The MIC50 and MIC90 values of the four fluoroquinolones for the three classes of S. pneumoniae (penicillin-susceptible, penicillin-intermediate and penicillin-resistant) were not significantly different. In contrast, the differences in in-vitro activity observed among the four fluoroquinolones against the 205 strains allowed them to be separated into three groups: sparfloxacin (MIC50/90 0.25 mg/L); ciprofloxacin and levofloxacin (MIC50 0.5 and 1 mg/L respectively, MIC90 1 mg/L); and ofloxacin (MIC50 1 mg/L, MIC90 2 mg/L). A total of 204 of the strains had a levofloxacin MIC between 0.25 mg/L and 1 mg/L, and only one of the 205 strains was highly resistant (MIC 16 mg/L). Whatever the level of susceptibility to penicillin, the relative bacteriostatic activity was, in descending order of activity, sparfloxacin, levofloxacin/ciprofloxacin and ofloxacin. These results suggest levofloxacin has potential for the treatment of pneumococcal infections.

摘要

本研究旨在比较左氧氟沙星与氧氟沙星、司帕沙星和环丙沙星对205株肺炎链球菌(101株对青霉素敏感、51株对青霉素中介和53株对青霉素耐药)的体外抑菌活性。这些分离株由参与全国肺炎球菌感染合作调查的法国医院于1996年9月至1996年10月提供。采用琼脂稀释法测定最低抑菌浓度(mg/L)。这四种氟喹诺酮类药物对三类肺炎链球菌(青霉素敏感、青霉素中介和青霉素耐药)的MIC50和MIC90值无显著差异。相比之下,观察到的这四种氟喹诺酮类药物对205株菌株的体外活性差异使它们可分为三组:司帕沙星(MIC50/90为0.25 mg/L);环丙沙星和左氧氟沙星(MIC50分别为0.5和1 mg/L,MIC90为1 mg/L);以及氧氟沙星(MIC50为1 mg/L,MIC90为2 mg/L)。共有204株菌株的左氧氟沙星MIC在0.25 mg/L至1 mg/L之间,并且205株菌株中只有1株高度耐药(MIC为16 mg/L)。无论对青霉素的敏感程度如何,相对抑菌活性按活性从高到低依次为司帕沙星、左氧氟沙星/环丙沙星和氧氟沙星。这些结果表明左氧氟沙星具有治疗肺炎球菌感染的潜力。

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