Jones R N, Pfaller M A, Doern G V
Department of Pathology, University of Iowa College of Medicine, Iowa City 52242, USA.
Diagn Microbiol Infect Dis. 1998 Oct;32(2):119-26. doi: 10.1016/s0732-8893(98)00072-8.
Trovafloxacin is a new fluorinated naphthyridone having expanded activity against Gram-positive and anaerobic pathogens compared with ciprofloxacin or levofloxacin or ofloxacin. A multicenter in vitro trial (201 sites) was initiated in late 1997 to study the comparative activity of trovafloxacin against Streptococcus pneumoniae strains during the recently completed respiratory disease season. Each laboratory was asked to test 20 to 30 recent isolates (3049 strains) by the Etest (AB BIODISK, Solna, Sweden) method with observed phenotypes with elevated trovafloxacin results (MIC, > 1 microgram/mL) confirmed by the monitor laboratory (University of Iowa College of Medicine). Approximately one-third (34.0%) of isolates were penicillin nonsusceptible (12.8% high-level resistance at > or = 2 micrograms/mL). Also 20.4% and 4.5% of strains were resistant to macrolides (erythromycin) and ceftriaxone, respectively. The macrolide resistance rate was lowered to 16.8% when the adverse effect of CO2 incubation was considered. Only 0.3% of S. pneumoniae were vancomycin-nonsusceptible using the current National Committee for Clinical Laboratory Standards breakpoint (< or = 1 microgram/mL) with nearly all results were at 1.5 micrograms/mL. Trovafloxacin (MIC50 and MIC90, 0.094 and 0.19 microgram/mL, respectively) was eight fold more potent than levofloxacin (MIC90, 0.75 and 1.5 micrograms/mL), and fewer strains (0.10%) were discovered with high-level resistance (MIC, > or = 8 micrograms/mL). The four resistant isolates from different states had alterations in both par C and gyr A. Trovafloxacin had the best potency observed against contemporary pneumococcal isolates, and has a spectrum (> 99.8% susceptible) for an orally administered agent that was comparable to the tested parenteral glycopeptide, vancomycin (> 99.7%). Blood and spinal-fluid culture isolates were generally more susceptible to penicillin (74.4 to 75.6%), other beta-lactams, and erythromycin (84.4%); throat and sputum isolates were significantly more resistant (p < 0.01). Increases in resistance among S. pneumoniae strains to beta-lactams and erythromycin were documented in all geographic regions monitored, other resistances also continue to evolve, and high-level fluoroquinolone resistance remains very rare.
曲伐沙星是一种新型的氟化萘啶酮,与环丙沙星、左氧氟沙星或氧氟沙星相比,它对革兰氏阳性菌和厌氧性病原体具有更广泛的活性。1997年末启动了一项多中心体外试验(201个位点),以研究曲伐沙星在最近结束的呼吸道疾病季节中对肺炎链球菌菌株的相对活性。要求每个实验室通过Etest(AB BIODISK,瑞典索尔纳)方法检测20至30株近期分离株(3049株),监测实验室(爱荷华大学医学院)确认曲伐沙星结果升高(MIC,>1微克/毫升)的观察表型。大约三分之一(34.0%)的分离株对青霉素不敏感(12.8%在>或=2微克/毫升时有高水平耐药)。此外,分别有20.4%和4.5%的菌株对大环内酯类(红霉素)和头孢曲松耐药。考虑到二氧化碳孵育的不利影响,大环内酯类耐药率降至16.8%。使用当前美国国家临床实验室标准委员会的断点(<或=1微克/毫升),只有0.3%的肺炎链球菌对万古霉素不敏感,几乎所有结果都在1.5微克/毫升。曲伐沙星(MIC50和MIC90分别为0.094和0.19微克/毫升)的效力比左氧氟沙星(MIC90为0.75和1.5微克/毫升)高8倍,发现高水平耐药(MIC,>或=8微克/毫升)的菌株较少(0.10%)。来自不同州的4株耐药分离株在par C和gyr A中均有改变。曲伐沙星对当代肺炎球菌分离株的效力最佳,对于口服制剂而言,其抗菌谱(>99.8%敏感)与受试的胃肠外糖肽万古霉素(>99.7%)相当。血液和脑脊液培养分离株通常对青霉素(74.4%至75.6%)、其他β-内酰胺类和红霉素(84.4%)更敏感;咽喉和痰液分离株的耐药性明显更高(p<0.01)。在所有监测的地理区域中,均记录到肺炎链球菌菌株对β-内酰胺类和红霉素的耐药性增加,其他耐药性也在不断演变,而高水平氟喹诺酮耐药性仍然非常罕见。