Department of Human Histology, CRPP, University of Liège, avenue de l'Hôpital 1, Sart Tilman, 4000 Liège, Belgium.
Department of Human Histology, CRPP, University of Liège, avenue de l'Hôpital 1, Sart Tilman, 4000 Liège, Belgium.
Int J Antimicrob Agents. 2015 Jul;46(1):33-8. doi: 10.1016/j.ijantimicag.2015.02.010. Epub 2015 Mar 18.
Recurrent Pseudomonas aeruginosa infections involving biofilm formation are frequent in cystic fibrosis, aggravating the respiratory distress. Co-administration of clarithromycin and classical tobramycin could improve the health status of patients. Antibiotic toxicity was assessed on epithelial (CFBE41o(-)) and macrophagic (THP-1) cell lines. Non-toxic concentrations of antibiotics alone or in combination were applied twice daily for 12 days on mature (12-day-old) biofilms of three P. aeruginosa strains, developed either in prokaryotic culture broth [tryptic soy broth (TSB)] or in a eukaryotic cell culture medium (RPMI-FCS) more similar to an in vivo environment. The antibiofilm and bactericidal effects of antibiotics were assessed. No toxicity of tobramycin was observed on eukaryotic cell lines at concentrations up to 500μg/mL, whilst 100μg/mL was selected as the clarithromycin upper safe limit. The amount of biofilm was strongly reduced by 100μg/mL and 500μg/mL tobramycin for each strain in both media, whilst clarithromycin was only effective in RPMI-FBS, with synergistic (PAO1 strain) and additive (PYO2 strain) effects detected when combining tobramycin 4μg/mL and clarithromycin 100μg/mL. Finally, tobramycin at ≥100μg/mL exerted strong bactericidal effects on each strain in both media. Clarithromycin also exerted bactericidal effects on each strain in both media; its effect was weaker than tobramycin in TSB but was similar in RPMI-FBS. Synergistic effects were observed on PAO1 and MUCO biofilms, e.g. when combining tobramycin 4μg/mL and clarithromycin 100μg/mL. These in vitro data show that co-administration of clarithromycin and tobramycin acts synergistically against in vitro P. aeruginosa biofilms.
反复出现的铜绿假单胞菌感染,涉及生物膜形成,在囊性纤维化中很常见,加重了呼吸窘迫。克拉霉素和经典妥布霉素联合使用可以改善患者的健康状况。在体外评估了上皮(CFBE41o(-))和巨噬(THP-1)细胞系中的抗生素毒性。单独或联合使用非毒性浓度的抗生素,每天两次,共 12 天,作用于三种铜绿假单胞菌菌株成熟(12 天龄)生物膜上,这些生物膜分别在原核培养肉汤[胰蛋白酶大豆肉汤(TSB)]或更类似于体内环境的真核细胞培养基(RPMI-FCS)中生长。评估了抗生素的抗生物膜和杀菌作用。在高达 500μg/mL 的浓度下,妥布霉素对真核细胞系没有毒性,而选择 100μg/mL 作为克拉霉素的安全上限。在两种培养基中,每种菌株的生物膜量均被 100μg/mL 和 500μg/mL 妥布霉素强烈减少,而克拉霉素仅在 RPMI-FBS 中有效,当联合使用 4μg/mL 妥布霉素和 100μg/mL 克拉霉素时,发现协同(PAO1 株)和累加(PYO2 株)作用。最后,妥布霉素在两种培养基中,浓度≥100μg/mL 时对每种菌株均具有强大的杀菌作用。克拉霉素在两种培养基中对每种菌株均具有杀菌作用;在 TSB 中的作用弱于妥布霉素,但在 RPMI-FBS 中相似。在 PAO1 和 MUCO 生物膜上观察到协同作用,例如,当联合使用 4μg/mL 妥布霉素和 100μg/mL 克拉霉素时。这些体外数据表明,克拉霉素和妥布霉素联合使用对体外铜绿假单胞菌生物膜具有协同作用。