Coldham Nick G, Randall Luke P, Piddock Laura J V, Woodward Martin J
Department of Food and Environmental Safety, Veterinary Laboratories Agency, Addlestone, Surrey, KT15 3NB, UK.
J Antimicrob Chemother. 2006 Dec;58(6):1145-53. doi: 10.1093/jac/dkl413. Epub 2006 Oct 24.
The physiological response of Salmonella enterica serovar Typhimurium to fluoroquinolone antibiotics was investigated using proteomic methods.
Proteomes were prepared from strain SL1344 following treatment of broth cultures with ciprofloxacin (0.03 and 0.008 mg/L; 2x and 0.5x MIC) and enrofloxacin (0.03 mg/L) and from a multiple antibiotic resistant (MAR) mutant. Protein expression was determined by two-dimensional HPLC-MS(n) and also after exposure to ciprofloxacin by two-dimensional gel electrophoresis (2D-GE).
The number of proteins (mean +/- SD) detected by 2D-GE derived from control cultures of the wild-type strain was significantly (P < 0.05) reduced from 296 +/- 77 to 153 +/- 36 following treatment with ciprofloxacin (0.03 mg/L). Raised expression (P < 0.05) of 17 proteins was also detected, and increases of up to 8-fold (P < 0.0001) were observed for subunits of F1F0-ATP synthase, TolC and Imp. Analysis by two-dimensional HPLC-MS(n) provided higher proteome coverage with 787 +/- 50 proteins detected, which was reduced (P < 0.005) to 560 +/- 14 by ciprofloxacin (0.03 mg/L). Increased expression of 43 proteins was observed which included those detected by 2D-GE and additionally the efflux pump protein AcrB. The basal expression of the AcrAB/TolC efflux pump was elevated in the MAR mutant compared with the untreated wild-type and augmented following treatment with ciprofloxacin (0.03 mg/L). F1F0-ATP synthase and Imp were only elevated in the mutant when treated with ciprofloxacin.
These studies suggest that increased expression of AcrAB/TolC was associated with resistance while other increases, such as in F1F0-ATP synthase and Imp, were a response to fluoroquinolone.
采用蛋白质组学方法研究肠炎沙门氏菌鼠伤寒血清型对氟喹诺酮类抗生素的生理反应。
用环丙沙星(0.03和0.008mg/L;2倍和0.5倍最低抑菌浓度)和恩诺沙星(0.03mg/L)处理肉汤培养物后的菌株SL1344以及多重耐药(MAR)突变体,制备蛋白质组。通过二维高效液相色谱-质谱联用(HPLC-MS(n))测定蛋白质表达,并用二维凝胶电泳(2D-GE)在环丙沙星处理后进行测定。
野生型菌株对照培养物经二维凝胶电泳检测到的蛋白质数量(平均值±标准差),在用环丙沙星(0.03mg/L)处理后从296±77显著(P<0.05)减少到153±36。还检测到17种蛋白质表达升高(P<0.05),F1F0-ATP合酶、TolC和Imp亚基的增加高达8倍(P<0.0001)。二维高效液相色谱-质谱联用分析提供了更高的蛋白质组覆盖率,检测到787±50种蛋白质,经环丙沙星(0.03mg/L)处理后减少(P<0.005)至560±14种。观察到43种蛋白质表达增加,包括二维凝胶电泳检测到的那些,以及额外的外排泵蛋白AcrB。与未处理的野生型相比,MAR突变体中AcrAB/TolC外排泵的基础表达升高,在用环丙沙星(0.03mg/L)处理后增强。F1F0-ATP合酶和Imp仅在突变体用环丙沙星处理时升高。
这些研究表明,AcrAB/TolC表达增加与耐药性相关,而其他增加,如F1F0-ATP合酶和Imp的增加,是对氟喹诺酮的反应。