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Sch 34343对链球菌和耐β-内酰胺类肠杆菌科细菌的活性。

Sch 34343 activity against streptococci and beta-lactam-resistant Enterobacteriaceae.

作者信息

Gutmann L, Kitzis M D, Acar J F

出版信息

J Antimicrob Chemother. 1985 Jun;15 Suppl C:147-54. doi: 10.1093/jac/15.suppl_c.147.

Abstract

The in-vitro activity of Sch 34343 was compared with that of cefotaxime, ceftazidime, latamoxef (moxalactam), aztreonam and ampicillin. Against pneumococci, Sch 34343 was as active as ampicillin, whereas against the other streptococci it was less active than ampicillin but significantly better than the other antibiotics against enterococci. With clinical isolates of Enterobacteriaceae resistant to cefotaxime, Sch 34343 had MICs generally less than 2 mg/l. After introduction of plasmid-mediated beta-lactamases into Escherichia coli Cla. there were no significant changes in the MICs of Sch 34343. Mutants of Enterobacter cloacae, Citrobacter freundii and Morganella morganii with derepressed cephalosporinases had susceptibilities equal to or less than 1 mg/l, which were generally lower than those of the other compounds tested. Comparison of parental strains and permeability mutants of E. coli, Ent. cloacae, and Serratia marcescens showed that the increase in MICs of Sch 34343 were lower than those found for the other antibiotics.

摘要

将Sch 34343的体外活性与头孢噻肟、头孢他啶、拉氧头孢(羟羧氧酰胺菌素)、氨曲南和氨苄西林的活性进行了比较。对于肺炎球菌,Sch 34343的活性与氨苄西林相当,而对于其他链球菌,其活性低于氨苄西林,但对肠球菌的活性明显优于其他抗生素。对于对头孢噻肟耐药的肠杆菌科临床分离株,Sch 34343的最低抑菌浓度(MIC)通常低于2mg/l。将质粒介导的β-内酰胺酶导入大肠杆菌Cla后,Sch 34343的MIC没有显著变化。头孢菌素酶去阻遏的阴沟肠杆菌、弗氏柠檬酸杆菌和摩根摩根菌突变体的敏感性等于或低于1mg/l,通常低于所测试的其他化合物。对大肠杆菌、阴沟肠杆菌和粘质沙雷氏菌的亲本菌株和通透性突变体进行比较表明,Sch 34343的MIC增加幅度低于其他抗生素。

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