Karlowsky J A, Hoban D J, Zelenitsky S A, Zhanel G G
Department of Medical Microbiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
J Antimicrob Chemother. 1997 Sep;40(3):371-6. doi: 10.1093/jac/40.3.371.
Adaptive resistance to aminoglycoside killing and cytoplasmic accumulation occurs in cultures of originally susceptible Pseudomonas aeruginosa following an initial incubation with aminoglycoside. Anaerobiosis has also been reported to reduce bacterial killing and limit cytoplasmic aminoglycoside accumulation. We hypothesized that a common mechanism may facilitate reduced bacterial killing and aminoglycoside accumulation in both cases. Northern blot analysis of P. aeruginosa adaptively resistant to gentamicin demonstrated increased mRNA levels of both denA (nitrite reductase), which facilitates terminal electron acceptance in the anaerobic respiratory pathway, and its regulatory protein, ANR, in the absence of promoter DNA sequence changes, when compared with controls. These observations suggested that P. aeruginosa may regulate the expression of genes in its anaerobic respiratory pathway in response to aminoglycosides and may explain, at least partially, P. aeruginosa adaptive resistance to aminoglycosides.
在最初用氨基糖苷类药物孵育后,原本对其敏感的铜绿假单胞菌培养物中会出现对氨基糖苷类药物杀伤作用和胞质积累的适应性耐药。据报道,厌氧环境也会减少细菌杀伤并限制胞质内氨基糖苷类药物的积累。我们推测,在这两种情况下,可能存在一种共同机制促进细菌杀伤减少和氨基糖苷类药物积累。与对照相比,对庆大霉素具有适应性耐药的铜绿假单胞菌的Northern印迹分析表明,在没有启动子DNA序列变化的情况下,促进厌氧呼吸途径中末端电子接受的denA(亚硝酸还原酶)及其调节蛋白ANR的mRNA水平均有所增加。这些观察结果表明,铜绿假单胞菌可能会响应氨基糖苷类药物调节其厌氧呼吸途径中基因的表达,这可能至少部分解释了铜绿假单胞菌对氨基糖苷类药物的适应性耐药。