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耐碳青霉烯鲍曼不动杆菌爆发与 COVID 大流行期间多粘菌素短缺有关:美罗培南、庆大霉素和舒巴坦之间协同作用的体外和生物膜分析。

A carbapenem-resistant Acinetobacter baumannii outbreak associated with a polymyxin shortage during the COVID pandemic: an in vitro and biofilm analysis of synergy between meropenem, gentamicin and sulbactam.

机构信息

Laboratory of Emerging Infectious Diseases, Pontifícia Universidade Católica do Paraná, Curitiba - PR, Brazil.

Hospital Universitário Evangélico Mackenzie, Curitiba - PR, Brazil.

出版信息

J Antimicrob Chemother. 2022 May 29;77(6):1676-1684. doi: 10.1093/jac/dkac102.

Abstract

BACKGROUND

During the COVID-19 pandemic, the burden of nosocomial infections caused by MDR pathogens has caused a shortage of polymyxins. Thus, we evaluated the in vitro synergism and antibiofilm activity of antimicrobial combinations and propose a test kit for synergism against carbapenem-resistant Acinetobacter baumannii (CRAB).

METHODS

Fifty-six CRAB isolates were tested for synergy between meropenem, gentamicin and ampicillin/sulbactam. MICs were determined by broth microdilution. Synergism was tested using chequerboard analysis, followed by a time-kill curve. Additionally, minimum biofilm eradication concentration was determined and the antibiofilm activity of the combinations was evaluated by MTT assay and biomass reduction. A test kit was developed for routine laboratory testing to detect synergism.

RESULTS

All CRAB isolates were resistant to gentamicin and ampicillin/sulbactam. Chequerboard synergism occurred against 75% of the isolates. Meropenem + ampicillin/sulbactam was the most frequent combination with synergism (69%), followed by ampicillin/sulbactam + gentamicin (64%) and meropenem + gentamicin (51%). All combinations presented only bacteriostatic activity and no bactericidal or antibiofilm effects. The routine laboratory test showed 100% accuracy compared with other in vitro assays.

CONCLUSIONS

Our study demonstrates the potential role of antibiotic combinations against planktonic bacteria. In vitro synergism is possible and can be an alternative treatment for patients with CRAB infection during a polymyxin shortage.

摘要

背景

在 COVID-19 大流行期间,耐多药病原体引起的医院感染负担导致多粘菌素短缺。因此,我们评估了抗菌药物组合的体外协同作用和抗生物膜活性,并提出了一种针对耐碳青霉烯鲍曼不动杆菌(CRAB)的协同作用检测试剂盒。

方法

对 56 株 CRAB 分离株进行了美罗培南、庆大霉素和氨苄西林/舒巴坦之间协同作用的检测。采用肉汤微量稀释法测定 MIC。采用棋盘试验检测协同作用,然后进行时间杀伤曲线试验。此外,还测定了最低生物膜清除浓度,并通过 MTT 测定和生物量减少评估组合的抗生物膜活性。开发了一种检测试剂盒,用于常规实验室检测以检测协同作用。

结果

所有 CRAB 分离株均对庆大霉素和氨苄西林/舒巴坦耐药。棋盘试验显示 75%的分离株存在协同作用。美罗培南+氨苄西林/舒巴坦是最常见的协同组合(69%),其次是氨苄西林/舒巴坦+庆大霉素(64%)和美罗培南+庆大霉素(51%)。所有组合均表现出仅抑菌活性,无杀菌或抗生物膜作用。与其他体外检测相比,常规实验室检测的准确性为 100%。

结论

我们的研究表明抗生素组合对浮游细菌具有潜在作用。体外协同作用是可能的,在多粘菌素短缺期间,可作为治疗 CRAB 感染患者的替代方法。

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