Al-Asadi M J, Towner K, Greenwood D
J Med Microbiol. 1981 May;14(2):171-83. doi: 10.1099/00222615-14-2-171.
The development of non-specific resistance ot gentamicin, tobramycin and amikacin was studied in 12 clinical isolates of enterobacteria with various patterns of aminoglycoside resistance. Strains were characterised with respect to MIC, transferability of resistance and possession of acetylating and adenylylating enzymes. An increase in aminoglycoside resistance was induced in 10 strains by a single exposure to the concentration of gentamicin, tobramycin or amikacin immediately below the MIC. Such resistance was non-specific; all three aminoglycosides were affected irrespective of which one had been used to induce the increase. Increments in non-specific aminoglycoside resistance were also evoked by exposure of enterobacteria to changing drug concentrations similar to those achieved in plasma during therapy. When strains already resistant to gentamicin or other aminoglycosides were exposed to therapeutically achievable drug concentrations, no further increase in resistance was observed in most cases. This suggests that use of an aminoglycoside to which the organism is resistant, as during "blind" therapy, will not usually compromise subsequent treatment with related antibiotics. The possible relevance of non-specific aminoglycoside resistance to therapy is discussed.
对12株具有不同氨基糖苷类耐药模式的肠杆菌临床分离株进行了对庆大霉素、妥布霉素和阿米卡星非特异性耐药性的研究。对菌株进行了最低抑菌浓度(MIC)、耐药性转移性以及乙酰化和腺苷酸化酶的检测。通过单次暴露于略低于MIC的庆大霉素、妥布霉素或阿米卡星浓度,在10株菌株中诱导出氨基糖苷类耐药性增加。这种耐药性是非特异性的;无论使用哪种氨基糖苷类诱导增加,所有三种氨基糖苷类均受影响。将肠杆菌暴露于与治疗期间血浆中达到的浓度相似的变化药物浓度下,也会引起非特异性氨基糖苷类耐药性增加。当已经对庆大霉素或其他氨基糖苷类耐药的菌株暴露于治疗可达到的药物浓度时,在大多数情况下未观察到耐药性进一步增加。这表明在“经验性”治疗期间使用生物体耐药的氨基糖苷类,通常不会影响随后使用相关抗生素的治疗。讨论了非特异性氨基糖苷类耐药性与治疗的可能相关性。