Turk J Med Sci. 2015;45(1):55-9. doi: 10.3906/sag-1307-18.
BACKGROUND/AIM: To detect the effects on quinolone resistance due to biofilm formation activity in Ureaplasma urealyticum.
An improved checkerboard dilution susceptibility test was used to analyze the quinolone resistance of clinical Ureaplasma isolates and a postbiofilm formation susceptibility assay was used to compare the effects on the quinolone susceptibility between pre- and postbiofilm formations. Several important functional gene expressions were detected to evaluate their roles in the process of the quinolone resistance mechanism.
The quinolone-resistant isolates produced more biofilms than the sensitive isolates. In both the quinolone-resistant and -sensitive groups, the minimal inhibitory concentrations after biofilm formation were higher than those before biofilm formation. The expression of the metabolism-related gene ureC in postbiofilm formation was higher than those in prebiofilm formation.
It seems that biofilm formation is quite important in the generation of quinolone resistance in Ureaplasma. It is very useful to detect biofilm formation activity as well as to analyze other laboratory parameters for Ureaplasma.
背景/目的:检测解脲脲原体生物膜形成活性对喹诺酮类药物耐药性的影响。
采用改良棋盘稀释药敏试验分析临床解脲脲原体分离株的喹诺酮耐药性,并采用生物膜形成后药敏试验比较生物膜形成前后对喹诺酮敏感性的影响。检测几种重要的功能基因表达,以评估它们在喹诺酮耐药机制中的作用。
喹诺酮耐药株比敏感株产生更多的生物膜。在喹诺酮耐药组和敏感组中,生物膜形成后的最小抑菌浓度均高于生物膜形成前。生物膜形成后代谢相关基因 ureC 的表达高于生物膜形成前。
生物膜形成似乎在解脲脲原体产生喹诺酮耐药性中非常重要。检测生物膜形成活性以及分析解脲脲原体的其他实验室参数非常有用。