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达托霉素对金黄色葡萄球菌和肠球菌属的体外活性。

The in vitro activity of daptomycin against Staphylococcus aureus and Enterococcus species.

作者信息

Richter S S, Kealey D E, Murray C T, Heilmann K P, Coffman S L, Doern G V

机构信息

Department of Pathology, C606 GH, University of Iowa Roy J. and Lucille A. Carver College of Medicine, Iowa City, Iowa 52242-1009, USA.

出版信息

J Antimicrob Chemother. 2003 Jul;52(1):123-7. doi: 10.1093/jac/dkg288. Epub 2003 Jun 12.

Abstract

OBJECTIVE

The purpose of this study was to examine the in vitro activity of daptomycin using an optimal calcium (Ca2+) concentration (50 mg/L) against a diverse collection of enterococcal and Staphylococcus aureus clinical isolates, including glycopeptide-resistant enterococci (GRE) and methicillin-resistant S. aureus (MRSA).

METHODS

The activity of daptomycin was compared with the activities of seven other agents against 1483 enterococcal and S. aureus clinical isolates, including 303 GRE and 193 methicillin-resistant S. aureus (MRSA) strains. Susceptibility testing was performed by the NCCLS broth microdilution method, with one exception: Mueller-Hinton (MH) broth was supplemented to a physiological level of 50 mg/L Ca2+ when testing daptomycin. Daptomycin zone diameters were determined by disc diffusion with MH agar plates containing Ca2+ 50 mg/L.

RESULTS

All staphylococcal isolates tested, and the majority of enterococcal isolates (96.5%), would be considered susceptible to daptomycin if the breakpoint previously proposed of </=2 mg/L was applied. The activity of daptomycin against MRSA and methicillin-susceptible S. aureus was essentially equal. Daptomycin also had similar activity against GRE and glycopeptide-susceptible enterococci. Every S. aureus isolate had a daptomycin zone diameter > or = 20 mm, and all of the enterococcal isolates had daptomycin zone diameters > or = 17 mm.

CONCLUSIONS

Overall, daptomycin showed potent activity against S. aureus and enterococcal isolates, comparable to quinupristin-dalfopristin and linezolid.

摘要

目的

本研究旨在使用最佳钙(Ca2+)浓度(50 mg/L)检测达托霉素对多种肠球菌和金黄色葡萄球菌临床分离株的体外活性,包括耐糖肽肠球菌(GRE)和耐甲氧西林金黄色葡萄球菌(MRSA)。

方法

将达托霉素的活性与其他七种药物对1483株肠球菌和金黄色葡萄球菌临床分离株的活性进行比较,其中包括303株GRE和193株耐甲氧西林金黄色葡萄球菌(MRSA)菌株。药敏试验采用NCCLS肉汤微量稀释法,但有一个例外:检测达托霉素时,将Mueller-Hinton(MH)肉汤补充至生理水平的50 mg/L Ca2+。达托霉素抑菌圈直径通过在含50 mg/L Ca2+的MH琼脂平板上进行纸片扩散法测定。

结果

如果采用先前提出的≤2 mg/L的折点,则所有测试的葡萄球菌分离株以及大多数肠球菌分离株(96.5%)可被认为对达托霉素敏感。达托霉素对MRSA和甲氧西林敏感金黄色葡萄球菌的活性基本相同。达托霉素对GRE和糖肽敏感肠球菌也具有相似的活性。每株金黄色葡萄球菌分离株的达托霉素抑菌圈直径≥20 mm,所有肠球菌分离株的达托霉素抑菌圈直径≥17 mm。

结论

总体而言,达托霉素对金黄色葡萄球菌和肠球菌分离株显示出强效活性,与奎奴普丁-达福普汀和利奈唑胺相当。

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