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舒巴坦与阿维巴坦或杜洛巴坦对耐碳青霉烯类细菌的比较活性。

Comparative activity of sulbactam with avibactam or durlobactam against carbapenem-resistant .

作者信息

Dorazio Ava J, Kline Ellen G, Squires Kevin M, Griffith Marissa P, Doi Yohei, Shields Ryan K

机构信息

Department of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, PA, USA.

Center for Innovative Antimicrobial Therapy, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

JAC Antimicrob Resist. 2025 Jun 23;7(3):dlaf098. doi: 10.1093/jacamr/dlaf098. eCollection 2025 Jun.

Abstract

OBJECTIVE

To determine the activity of sulbactam in combination with avibactam or durlobactam with and without meropenem or imipenem against carbapenem-resistant clinical isolates.

METHODS

Standardized susceptibility testing by broth microdilution was performed to determine MICs for imipenem, meropenem and sulbactam alone, and for combinations including sulbactam/avibactam, sulbactam/durlobactam, sulbactam/avibactam/meropenem, sulbactam/avibactam/imipenem, sulbactam/durlobactacm/meropenem and sulbactam/durlobactam/imipenem. Whole-genome sequencing was also performed to compare MICs to key resistance determinants, including mutations in penicillin-binding proteins (PBPs).

RESULTS

Median sulbactam/durlobactam and sulbactam/avibactam MICs were 2 and 16 mg/L, respectively. Imipenem potentiated the activity of both combinations to a greater extent than meropenem corresponding to median sulbactam/durlobactam/imipenem and sulbactam/avibactam/imipenem MICs of 1 and 8 mg/L, respectively. Carbapenem combinations were more active than combinations without a carbapenem against isolates with PBP3 mutations.

CONCLUSIONS

These data show that imipenem potentiates sulbactam-based combinations to a greater extent than meropenem; however, future studies are needed to define how these data should be applied in clinical practice.

摘要

目的

确定舒巴坦与阿维巴坦或杜洛巴坦联合使用,以及联合美罗培南或亚胺培南对耐碳青霉烯临床分离株的活性。

方法

采用肉汤微量稀释法进行标准化药敏试验,以确定亚胺培南、美罗培南和舒巴坦单独使用时的最低抑菌浓度(MIC),以及舒巴坦/阿维巴坦、舒巴坦/杜洛巴坦、舒巴坦/阿维巴坦/美罗培南、舒巴坦/阿维巴坦/亚胺培南、舒巴坦/杜洛巴坦/美罗培南和舒巴坦/杜洛巴坦/亚胺培南联合使用时的MIC。还进行了全基因组测序,以将MIC与关键耐药决定因素进行比较,包括青霉素结合蛋白(PBPs)的突变。

结果

舒巴坦/杜洛巴坦和舒巴坦/阿维巴坦的MIC中位数分别为2 mg/L和16 mg/L。亚胺培南比美罗培南更能增强两种联合用药的活性,舒巴坦/杜洛巴坦/亚胺培南和舒巴坦/阿维巴坦/亚胺培南的MIC中位数分别为1 mg/L和8 mg/L。对于具有PBP3突变的分离株,含碳青霉烯的联合用药比不含碳青霉烯的联合用药更具活性。

结论

这些数据表明,亚胺培南比美罗培南更能增强基于舒巴坦的联合用药的活性;然而,需要进一步研究来确定如何将这些数据应用于临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/050a/12205954/1ede384b95b9/dlaf098f1.jpg

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