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用万古霉素-精氨酸靶向大肠杆菌。

Targeting of Escherichia coli with Vancomycin-Arginine.

作者信息

Neville Lewis F, Shalit Itamar, Warn Peter A, Scheetz Marc H, Sun Jiuzhi, Chosy Madeline B, Wender Paul A, Cegelski Lynette, Rendell Jacob T

机构信息

SuperTrans Medical Ltd., Ness Ziona, Israel

SuperTrans Medical Ltd., Ness Ziona, Israel.

出版信息

Antimicrob Agents Chemother. 2021 Mar 18;65(4). doi: 10.1128/AAC.02416-20.

Abstract

The ability of vancomycin-arginine (V-r) to extend the spectrum of activity of glycopeptides to Gram-negative bacteria was investigated. Its MIC towards , including β-lactamase expressing Ambler classes A, B, and D, was 8 to 16 μg/ml. Addition of 8 times the MIC of V-r to was acutely bactericidal and associated with a low frequency of resistance (<2.32 × 10). , V-r markedly reduced burden by >7 log CFU/g in a thigh muscle model. These data warrant further development of V-r in combatting , including resistant forms.

摘要

研究了万古霉素-精氨酸(V-r)将糖肽类抗生素的活性谱扩展至革兰氏阴性菌的能力。其对包括表达A、B和D类安布勒β-内酰胺酶的菌株的最低抑菌浓度(MIC)为8至16μg/ml。将8倍MIC的V-r添加至菌株中具有急性杀菌作用,且耐药频率较低(<2.32×10)。此外,在大腿肌肉模型中,V-r使菌株负荷显著降低>7 log CFU/g。这些数据表明V-r在对抗包括耐药形式在内的菌株方面值得进一步研发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67f7/8097466/3f76a9788ebe/AAC.02416-20-f0001.jpg

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