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[铜绿假单胞菌对β-内酰胺类抗生素的敏感性及β-内酰胺酶的作用]

[Sensitivity of Pseudomonas aeruginosa to beta-lactam antibiotics and effects of beta-lactamases].

作者信息

Avril J L, Cayla A M, Guist'hau O, Moillo-Batt A

出版信息

Pathol Biol (Paris). 1983 Jun;31(6):471-5.

PMID:6410345
Abstract

The activities of carbenicillin, ticarcillin, piperacillin, cefsulodin, ceftriaxone, azlocillin, ceftazidime and apalcillin were evaluated against 128 hospital isolates of Pseudomonas aeruginosa. Against the 85 isolates that were susceptible to carbenicillin, apalcillin had the best minimal inhibitory concentrations, the median MIC being 1, 1 microgram/ml. Against the 43 isolates resistant to carbenicillin, ceftazidime inhibited 90% of organisms at a concentration of 16 micrograms/ml. A constitutive beta-lactamase, was found in 27 of the 43 resistant isolates. All the 128 isolates, but one, were producers of an inducers of an inducible beta-lactamase. Ceftriaxone, piperacillin and azlocillin were highly antagonized by cefoxitin. The extent of antagonism was lower with ticarcillin and carbenicillin.

摘要

对128株医院分离的铜绿假单胞菌进行了羧苄西林、替卡西林、哌拉西林、磺苄西林、头孢曲松、阿洛西林、头孢他啶和阿帕西林的活性评估。对于85株对羧苄西林敏感的菌株,阿帕西林的最低抑菌浓度最佳,MIC中位数为1微克/毫升。对于43株对羧苄西林耐药的菌株,头孢他啶在浓度为16微克/毫升时可抑制90%的菌株。在43株耐药菌株中有27株发现有组成型β-内酰胺酶。除1株外,所有128株菌株均为诱导型β-内酰胺酶诱导剂的产生菌。头孢曲松、哌拉西林和阿洛西林被头孢西丁高度拮抗。替卡西林和羧苄西林的拮抗程度较低。

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