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HMR 3647对肺炎链球菌、流感嗜血杆菌、卡他莫拉菌和β溶血性链球菌的体外活性。

In-vitro activity of HMR 3647 against Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and beta-haemolytic streptococci.

作者信息

Wootton M, Bowker K E, Janowska A, Holt H A, MacGowan A P

机构信息

Bristol Centre for Antimicrobial Research and Evaluation, Southmead Health Services NHS Trust, UK.

出版信息

J Antimicrob Chemother. 1999 Oct;44(4):445-53. doi: 10.1093/jac/44.4.445.

Abstract

The in-vitro activity of HMR 3647 and seven comparators (azithromycin, clarithromycin, erythromycin A, roxithromycin, penicillin G, ciprofloxacin and levofloxacin) were tested against 207 Streptococcus pneumoniae and 200 beta-haemolytic streptococci. Ten comparators (azithromycin, clarithromycin, erythromycin A, roxithromycin, ampicillin, co-amoxiclav, cefuroxime, cefotaxime, ciprofloxacin and levofloxacin) were tested against 143 Haemophilus influenzae and 58 Moraxella catarrhalis. The MIC50 of HMR 3647 for S. pneumoniae was < or =0.008 mg/L, less than that for the macrolides or quinolones tested. Pneumococci with an erythromycin A MIC of 0.06 mg/L (n = 23) had an MIC50 of HMR 3647 < or =0.008 mg/L, whereas isolates with an erythromycin A MIC > or =1 mg/L (n = 34) had an MIC50 of HMR 3647 of 0.03 mg/L, a four-fold increase. In contrast, the difference in macrolide MIC50s for the two groups was > or =64-fold. The MIC50s foro beta-haemolytic streptococci, classified by Lancefield group, were in the range 0.015 to 0.06 mg/L for HMR 3647. H. influenzae were categorized into three groups according to cefuroxime MIC: <1 mg/L (n = 72); 2-4 mg/L (n = 29); and >4 mg/L (n = 42). The MIC50 of HMR 3647 increased two-fold with increasing cefuroxime MICs; beta-lactam MICs increased much more markedly. The MIC50 of HMR 3647 for M. catarrhalis was 0.03 mg/L. HMR 3647 has good activity against respiratory tract pathogens but in-vitro susceptibility is affected by erythromycin A susceptibility in S. pneumoniae and beta-haemolytic streptococci.

摘要

测试了HMR 3647及七种对照药物(阿奇霉素、克拉霉素、红霉素A、罗红霉素、青霉素G、环丙沙星和左氧氟沙星)对207株肺炎链球菌和200株β溶血性链球菌的体外活性。测试了十种对照药物(阿奇霉素、克拉霉素、红霉素A、罗红霉素、氨苄西林、阿莫西林克拉维酸、头孢呋辛、头孢噻肟、环丙沙星和左氧氟沙星)对143株流感嗜血杆菌和58株卡他莫拉菌的体外活性。HMR 3647对肺炎链球菌的MIC50≤0.008mg/L,低于所测试的大环内酯类或喹诺酮类药物。红霉素A MIC为0.06mg/L的肺炎链球菌(n = 23),HMR 3647的MIC50≤0.008mg/L;而红霉素A MIC≥1mg/L的菌株(n = 34),HMR 3647的MIC50为0.03mg/L,增加了四倍。相比之下,两组大环内酯类药物的MIC50差异≥64倍。根据兰斯菲尔德分组,HMR 3647对β溶血性链球菌的MIC50在0.015至0.06mg/L范围内。流感嗜血杆菌根据头孢呋辛MIC分为三组:<1mg/L(n = 72);2 - 4mg/L(n = 29);>4mg/L(n = 42)。随着头孢呋辛MIC增加,HMR 3647的MIC50增加两倍;β内酰胺类药物的MIC增加更为明显。HMR 3647对卡他莫拉菌的MIC50为0.03mg/L。HMR 3647对呼吸道病原体具有良好活性,但体外敏感性受肺炎链球菌和β溶血性链球菌中红霉素A敏感性的影响。

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