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沙门氏菌对抗菌药物的体外敏感性

In-vitro susceptibility of salmonellae to antimicrobial agents.

作者信息

Goossens H, Vanhoof R, De Mol P, Grados O, Ghysels G, Butzler J P

出版信息

J Antimicrob Chemother. 1984 Jun;13(6):559-65. doi: 10.1093/jac/13.6.559.

Abstract

The minimum inhibitory concentrations (MIC) of various antimicrobial drugs, for 667 strains of Salmonella, isolated in three different continents of the world, were determined: 17 antibiotics were tested against 506 randomly selected and 161 chloramphenicol-resistant strains. The activity of the monobactam aztreonam against these organisms was in general equal or superior to that observed with the third-generation cephalosporins, cefotaxime and ceftazidime. Furthermore aztreonam and cefotaxime exhibited uniform and high activity against all the salmonella strains tested, irrespective of their chloramphenicol resistance. Ceftazidime was found to have higher geometric mean MICs only for non-typhi salmonellae from Peru.

摘要

测定了从世界三大洲分离出的667株沙门氏菌对各种抗菌药物的最低抑菌浓度(MIC):对506株随机挑选的菌株以及161株耐氯霉素菌株测试了17种抗生素。单环β-内酰胺类药物氨曲南对这些菌株的活性总体上等于或优于第三代头孢菌素头孢噻肟和头孢他啶。此外,氨曲南和头孢噻肟对所有测试的沙门氏菌菌株均表现出一致的高活性,无论其对氯霉素的耐药性如何。仅发现头孢他啶对来自秘鲁的非伤寒沙门氏菌具有较高的几何平均MIC。

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