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Emergence of resistance to beta-lactam and aminoglycoside antibiotics during moxalactam therapy of Pseudomonas aeruginosa infections.

机译:莫拉西坦治疗铜绿假单胞菌感染期间对β-内酰胺和氨基糖苷类抗生素产生抗药性。

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摘要

In four patients with Pseudomonas aeruginosa infections, the infecting strain developed resistance to moxalactam during therapy with this drug. In addition, P. aeruginosa isolates from two of these four patients showed increased resistance to aminoglycosides. Isolates from a third patient acquired cross-resistance to other antipseudomonal beta-lactams. In three of the cases, disk susceptibility tests failed to detect the resistance that was demonstrated in broth dilution assays. Isolate identities were confirmed by serotyping. No new plasmids were found by agarose gel electrophoresis. The mechanisms for this resistance did not involve enzymatic antibiotic degradation. These findings suggest that currently available expanded-spectrum cephalosporin derivatives should probably not be used alone for most serious infections due to P. aeruginosa. They also suggest that strains with multiple antibiotic resistance may become more prevalent in hospitals if these drugs are used extensively.
机译:在四名铜绿假单胞菌感染患者中,感染菌株在用这种药物治疗期间对莫拉内酰胺产生了抗药性。另外,来自这四名患者中的两名的铜绿假单胞菌分离株显示出对氨基糖苷的抗性增加。来自第三例患者的分离株对其他抗假性β-内酰胺类药物具有交叉耐药性。在三种情况下,磁盘敏感性测试未能检测到肉汤稀释测定法所显示的抗药性。通过血清分型确认分离的身份。琼脂糖凝胶电泳未发现新质粒。这种抗药性的机制不涉及酶促抗生素降解。这些发现表明,目前可用的广谱头孢菌素衍生物可能不应单独用于因铜绿假单胞菌引起的最严重的感染。他们还建议,如果广泛使用具有多种抗生素耐药性的菌株,则在医院中可能会变得更加普遍。

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