Baltch Aldona L, Bopp Lawrence H, Smith Raymond P, Michelsen Phyllis B, Ritz William J
Infectious Disease Section, Stratton VA Medical Center, Albany, NY 12208, USA.
J Antimicrob Chemother. 2005 Jul;56(1):104-9. doi: 10.1093/jac/dki186. Epub 2005 Jun 7.
The antibacterial activity of a new fluoroquinolone, gemifloxacin, was tested against intracellular Legionella pneumophila and Legionella micdadei and was compared with the activities of levofloxacin, gatifloxacin, moxifloxacin and erythromycin.
For intracellular assays, bacteria were used to infect human monocyte-derived macrophages prepared from heparinized blood of healthy volunteers. Antibiotics were added following phagocytosis. Numbers of viable bacteria were determined at 0, 24, 48, 72 and 96 h.
The intracellular antibacterial activity of gemifloxacin was concentration- and time-dependent. All of the quinolones had similar activities against L. pneumophila and L. micdadei at 10 x MIC, but there were minor differences: at 24 h moxifloxacin was significantly more active than the other quinolones against L. pneumophila, while gemifloxacin was more active against L. micdadei (P < 0.01). All of the quinolones were markedly more active than erythromycin (P < 0.01). The antibacterial effect of gemifloxacin against L. pneumophila following drug removal at 24 h persisted for 72 h at 20 x MIC but not at 10 x MIC, while for L. micdadei the antibacterial effect persisted for 24 h at 10 x MIC.
All of the quinolones had similar activities against intracellular L. pneumophila and L. micdadei and were markedly more effective than erythromycin.
测试新型氟喹诺酮类药物吉米沙星对细胞内嗜肺军团菌和米克戴德军团菌的抗菌活性,并与左氧氟沙星、加替沙星、莫西沙星及红霉素的活性进行比较。
进行细胞内试验时,用细菌感染从健康志愿者肝素化血液中制备的人单核细胞衍生巨噬细胞。吞噬作用后添加抗生素。在0、24、48、72和96小时测定活菌数量。
吉米沙星的细胞内抗菌活性呈浓度和时间依赖性。所有喹诺酮类药物在10倍最低抑菌浓度(MIC)时对嗜肺军团菌和米克戴德军团菌具有相似活性,但存在细微差异:在24小时时,莫西沙星对嗜肺军团菌的活性显著高于其他喹诺酮类药物,而吉米沙星对米克戴德军团菌的活性更高(P<0.01)。所有喹诺酮类药物的活性均显著高于红霉素(P<0.01)。在24小时去除药物后,吉米沙星对嗜肺军团菌的抗菌作用在20倍MIC时持续72小时,但在10倍MIC时则不然;而对于米克戴德军团菌,抗菌作用在10倍MIC时持续24小时。
所有喹诺酮类药物对细胞内嗜肺军团菌和米克戴德军团菌具有相似活性,且比红霉素显著更有效。