Examining the Combination of Cefixime and Amoxicillin/Clavulanate against Extended-Spectrum Beta-Lactamase-Producing Escherichia coli Isolates.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Haedi Thelen, Thomas J Dilworth, Renée-Claude Mercier
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引用次数: 0

Abstract

Introduction: Community-acquired urinary tract infections (UTIs) caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli have limited oral therapeutic options and pose significant clinical challenges. The goal of this study was to evaluate the in vitro synergy between CFM and AMC against ESBL E. coli with aims to identify an oral treatment option for UTIs.

Methods: Minimum inhibitory concentrations (MICs) of CFM in the presence of AMC were determined for 46 clinical isolates by placing a CFM Etest on a plate with AMC impregnated in the agar. Isolates with CFM MIC ≤1 μg/mL in the presence of AMC were considered susceptible to the CFM and AMC combination. Five isolates were then selected for further testing using time-kill analysis in the presence of CFM, AMC, and CFM with AMC. Time-kill curves were plotted to determine synergy over 24 h.

Results: AMC improved the activity of CFM against ESBL E. coli isolates by 128-fold in the Etest analysis with 85% of tested isolates being susceptible to the combination. A fourfold or greater reduction in CFM MIC was exhibited in 44 of 46 (96%) isolates when in the presence of AMC. Synergy and bactericidal activity between CFM and AMC were exhibited in each of the five isolates tested by time-kill analysis.

Discussion/conclusion: This study found that AMC improves the activity of CFM against ESBL E. coli and that this antibiotic combination has potential as an oral therapeutic option to treat ESBL E. coli UTIs.

头孢克肟与阿莫西林/克拉维酸联合应用对广谱β -内酰胺酶产大肠杆菌的研究。
由产广谱β -内酰胺酶(ESBL)的大肠杆菌引起的社区获得性尿路感染(uti)的口服治疗选择有限,并构成重大的临床挑战。本研究的目的是评估CFM和AMC对ESBL大肠杆菌的体外协同作用,目的是确定一种口服治疗uti的选择。方法:通过将CFM est放置在浸染了AMC的琼脂板上,测定了46个临床分离株在AMC存在下CFM的最低抑制浓度(mic)。在AMC存在的情况下,CFM MIC≤1 μg/mL的分离株被认为对CFM和AMC联合敏感。然后选择5个分离株,在CFM、AMC和CFM合并AMC存在的情况下进行进一步的时间杀伤分析。结果:在Etest分析中,AMC将CFM对ESBL大肠杆菌的活性提高了128倍,85%的被试菌株对该组合敏感。当存在AMC时,46个分离株中有44个(96%)的CFM MIC降低了4倍或更多。时间杀伤分析表明,CFM与AMC均具有协同作用和杀菌活性。讨论/结论:本研究发现,AMC提高了CFM对ESBL大肠杆菌的活性,并且这种抗生素组合有可能作为治疗ESBL大肠杆菌尿路感染的口服治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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