Can Füsun, Kaya Melek, Bayindir Bilman Fulya, Uncu Hikmet, Demirbilek Müge, Yazici A Canan
Başkent Universitesi Tip Fakültesi, Mikrobiyoloji ve Klinik Mikrobiyoloji Anabilim Dali, Ankara.
Mikrobiyol Bul. 2009 Oct;43(4):587-95.
Acinetobacter baumannii is an important pathogen, capable of survival for very long periods on various surfaces in the hospital environment. Tigecycline is a commonly used antimicrobial agent especially for the treatment of resistant infections. The aim of this study was to investigate the activity of tigecycline on both planktonic and sessile biofilm cells of A. baumannii strains isolated from blood cultures and to compare the efficiency in terms of biofilm synthesis. Tigecycline activity on 59 A. baumannii strains was examined by agar dilution technique. The ability of strains to form biofilm was evaluated by adherence on polystyrene surfaces in brain heart infusion broth supplemented with 0.25% glucose. Time-kill technique was used for determination of the time and concentration dependent activity of tigecycline on biofilm positive and negative strains. The planktonic cells in logarithmic growth phase were exposed to tigecycline at 0.5, 1, 2, 4, ve 8 x minimum inhibitory concentration (MIC) concentrations and colony counts were evaluated after 0, 2, 4, 6, 24 and 48 hours. The effect of tigecycline on sessile cells was studied on biofilm matrix composed around plastic beads. Tigecycline susceptibility rate of planktonic cells was 89.8% and MIC50 and MIC90 values were 1 and 2 microg/ml, respectively. Biofilm formation was detected in 52.5% of isolates and no significant correlation was found between MIC values and biofilm production of the strains (p > 0.05). Tigecycline showed a potent antibacterial activity against planktonic cells regardless of biofilm forming capability of strains. Biofilm inhibitory concentrations of sessile cells were elevated significantly. As a result, tigecycline showed a potent activity on planktonic A. baumannii cells however, the effect was decreased significantly on sessile cells in biofilm environment. The results suggest that, the possibility of decreased sensitivity of cells in biofilm environment should be considered as well as antibiotic sensitivity test results during the treatment of infections caused by A. baumannii.
鲍曼不动杆菌是一种重要的病原体,能够在医院环境中的各种表面存活很长时间。替加环素是一种常用的抗菌药物,尤其用于治疗耐药感染。本研究的目的是调查替加环素对从血培养中分离出的鲍曼不动杆菌菌株的浮游菌和固着生物膜细胞的活性,并比较生物膜合成方面的效率。采用琼脂稀释技术检测替加环素对59株鲍曼不动杆菌菌株的活性。通过在补充有0.25%葡萄糖的脑心浸液肉汤中聚苯乙烯表面的黏附来评估菌株形成生物膜的能力。采用时间杀菌技术测定替加环素对生物膜阳性和阴性菌株的时间和浓度依赖性活性。将对数生长期的浮游菌暴露于0.5、1、2、4和8倍最小抑菌浓度(MIC)的替加环素中,并在0、2、4、6、24和48小时后评估菌落计数。在塑料珠周围形成的生物膜基质上研究替加环素对固着细胞的作用。浮游菌的替加环素敏感率为89.8%,MIC50和MIC90值分别为1和2μg/ml。52.5%的分离株检测到生物膜形成,菌株的MIC值与生物膜产生之间未发现显著相关性(p>0.05)。无论菌株的生物膜形成能力如何,替加环素对浮游菌均显示出强大的抗菌活性。固着细胞的生物膜抑制浓度显著升高。结果表明,替加环素对浮游鲍曼不动杆菌细胞具有强大的活性,然而,在生物膜环境中对固着细胞的作用显著降低。结果表明,在治疗鲍曼不动杆菌引起的感染时,除了抗生素敏感性试验结果外,还应考虑生物膜环境中细胞敏感性降低的可能性。