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由BMS-284756筛选出的金黄色葡萄球菌突变体。

Staphylococcus aureus mutants selected by BMS-284756.

作者信息

Discotto L F, Lawrence L E, Denbleyker K L, Barrett J F

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Infectious Diseases, Department of Microbiology, Wallingford, Connecticut 06492, USA.

出版信息

Antimicrob Agents Chemother. 2001 Nov;45(11):3273-5. doi: 10.1128/AAC.45.11.3273-3275.2001.

Abstract

BMS-284756, a novel des-fluoro(6)-quinolone, was used to select for in vitro mutants of Staphylococcus aureus ISP794. Step mutants were obtained, and the quinolone resistance-determining regions of four target genes, gyrA, gyrB, grlA, and grlB, were sequenced. The data suggest that DNA gyrase is the primary target for BMS-284756 in S. aureus.

摘要

新型去氟(6)-喹诺酮BMS-284756用于筛选金黄色葡萄球菌ISP794的体外突变体。获得了逐步突变体,并对四个靶基因gyrA、gyrB、grlA和grlB的喹诺酮耐药决定区进行了测序。数据表明,DNA回旋酶是BMS-284756在金黄色葡萄球菌中的主要靶点。

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2
Antibacterial spectrum of a novel des-fluoro(6) quinolone, BMS-284756.
Antimicrob Agents Chemother. 2000 Dec;44(12):3351-6. doi: 10.1128/AAC.44.12.3351-3356.2000.
3
Mechanisms and frequency of resistance to premafloxacin in Staphylococcus aureus: novel mutations suggest novel drug-target interactions.
Antimicrob Agents Chemother. 2000 Dec;44(12):3344-50. doi: 10.1128/AAC.44.12.3344-3350.2000.
6
In vitro and in vivo antibacterial activities of AM-1155, a new 6-fluoro-8-methoxy quinolone.
Antimicrob Agents Chemother. 1992 Oct;36(10):2108-17. doi: 10.1128/AAC.36.10.2108.

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