Jones Ronald N, Sader Helio S, Stilwell Matthew G, Fritsche Thomas R
JMI Laboratories, North Liberty, IA 52317, USA.
Diagn Microbiol Infect Dis. 2007 May;58(1):1-7. doi: 10.1016/j.diagmicrobio.2007.01.019. Epub 2007 Apr 3.
Community-acquired pneumonia (CAP) continues to cause significant morbidity worldwide, and the principal bacterial pathogens (Streptococcus pneumoniae and Haemophilus influenzae) have acquired numerous resistance mechanisms over the last few decades. CAP treatment guidelines have suggested the use of broader spectrum agents, such as antipneumococcal fluoroquinolones as the therapy for at-risk patient population. In this report, we studied 3087 CAP isolates from the SENTRY Antimicrobial Surveillance Program (1999-2005) worldwide and all respiratory tract infection (RTI) isolate population of pneumococci (14665 strains) grouped by antibiogram patterns against a new des-F(6)-quinolone, garenoxacin. Results indicated that garenoxacin was highly active against CAP isolates of S. pneumoniae (MIC(90), 0.06 microg/mL) and H. influenzae (MIC(90), < or =0.03 microg/mL). This garenoxacin potency was 8- to 32-fold greater than gatifloxacin, levofloxacin, and ciprofloxacin against the pneumococci and >99.9% of strains were inhibited at < or =1 microg/mL (proposed susceptible breakpoint). Garenoxacin MIC values were not affected by resistances among S. pneumoniae strains to penicillin or erythromycin; however, coresistances were high among the beta-lactams (penicillins and cephalosporins), macrolides, tetracyclines, and trimethoprim/sulfamethoxazole. Analysis of S. pneumoniae isolates with various antimicrobial resistance patterns to 6 drug classes demonstrated that garenoxacin was active against >99.9% (MIC, < or =1 microg/mL) of strains, and the most resistant pneumococci (6-drug resistance, 1051 strains or 7.2% of all isolates) were completely susceptible (100.0% at < or =1 microg/mL) to garenoxacin (MIC(90), 0.06 microg/mL). These results illustrate the high activity of garenoxacin against contemporary CAP isolates and especially against multidrug-resistant (MDR) S. pneumoniae that have created therapeutic dilemmas for all RTI presentations. Garenoxacin appears to be a welcome addition to the CAP treatment options, particularly for the emerging MDR pneumococci strains.
社区获得性肺炎(CAP)在全球范围内仍导致大量发病,在过去几十年中,主要的细菌病原体(肺炎链球菌和流感嗜血杆菌)已获得多种耐药机制。CAP治疗指南建议使用更广泛的抗菌药物,如抗肺炎球菌氟喹诺酮类药物,用于治疗高危患者群体。在本报告中,我们研究了来自全球哨兵抗菌监测计划(1999 - 2005年)的3087株CAP分离株以及所有呼吸道感染(RTI)肺炎球菌分离株群体(14665株),根据对一种新型去F(6)-喹诺酮类药物加替沙星的抗菌谱模式进行分组。结果表明,加替沙星对肺炎链球菌的CAP分离株(MIC(90),0.06μg/mL)和流感嗜血杆菌(MIC(90),≤0.03μg/mL)具有高度活性。加替沙星对肺炎球菌的活性比加替沙星、左氧氟沙星和环丙沙星高8至32倍,并且>99.9%的菌株在≤1μg/mL(建议的敏感断点)时被抑制。加替沙星的MIC值不受肺炎链球菌对青霉素或红霉素耐药性的影响;然而,β-内酰胺类(青霉素和头孢菌素)、大环内酯类、四环素类和甲氧苄啶/磺胺甲恶唑之间的共同耐药性很高。对具有6种药物类别的各种抗菌耐药模式的肺炎链球菌分离株进行分析表明,加替沙星对>99.9%(MIC,≤1μg/mL)的菌株具有活性,并且最耐药的肺炎球菌(6重耐药,1051株或所有分离株的7.2%)对加替沙星(MIC(90),0.06μg/mL)完全敏感(在≤1μg/mL时为100.0%)。这些结果表明加替沙星对当代CAP分离株具有高活性,特别是对给所有RTI表现带来治疗难题的多重耐药(MDR)肺炎链球菌。加替沙星似乎是CAP治疗选择中一个受欢迎的补充,特别是对于新出现的MDR肺炎球菌菌株。