Park B H, Levy S B
Department of Molecular Biology, Tufts University School of Medicine, Boston, Massachusetts.
Antimicrob Agents Chemother. 1988 Dec;32(12):1797-800. doi: 10.1128/AAC.32.12.1797.
Escherichia coli containing the cryptic tetracycline resistance determinant (class F) from the Bacteroides fragilis transposon Tn4400 on plasmid pGAT400 expressed a detoxification of tetracycline as well as an active efflux of tetracycline. This finding concurs with the report of detoxification for a related tetracycline resistance determinant from B. fragilis on Tn4351 (B. S. Speer and A. Salyers, J. Bacteriol. 170:1423-1429, 1987), which specifies a 10-fold-higher resistance than Tn4400. Inactivation of tetracycline occurred at an initial rate of congruent to 0.7 micrograms of tetracycline per h per 10(8) cells, as determined by biologic assay and chromatographic analysis. The detoxification is a chemical degradation which can occur in the absence of energy-dependent efflux. The products of this degradation were not substrates for active transport into susceptible cells or out of pGAT400-containing E. coli. These results indicate that Tn4400 mediates two functionally different mechanisms for tetracycline resistance: an active efflux of tetracycline and a degradation of tetracycline.
含有来自脆弱拟杆菌转座子Tn4400的隐秘四环素抗性决定簇(F类)的大肠杆菌,在质粒pGAT400上表达了四环素解毒作用以及四环素的主动外排。这一发现与关于Tn4351上来自脆弱拟杆菌的相关四环素抗性决定簇的解毒作用的报告一致(B.S.斯皮尔和A.萨利尔斯,《细菌学杂志》170:1423 - 1429, 1987),该决定簇指定的抗性比Tn4400高10倍。通过生物学测定和色谱分析确定,四环素失活的初始速率约为每小时每10⁸个细胞0.7微克四环素。解毒作用是一种化学降解,在没有能量依赖的外排情况下也能发生。这种降解产物不是主动转运进入敏感细胞或从含有pGAT400的大肠杆菌中排出的底物。这些结果表明,Tn4400介导了两种功能不同的四环素抗性机制:四环素的主动外排和四环素的降解。