抄録
Objective To determine the in vitro activity of sulbactam in combination with avibactam or durlobactam with and without meropenem or imipenem against carbapenem-resistant Acinetobacter baumannii 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 in vitro 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.
| 本文言語 | 英語 |
|---|---|
| 論文番号 | dlaf098 |
| ジャーナル | JAC-Antimicrobial Resistance |
| 巻 | 7 |
| 号 | 3 |
| DOI | |
| 出版ステータス | 出版済み - 01-06-2025 |
| 外部発表 | はい |
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All Science Journal Classification (ASJC) codes
- 微生物学
- 免疫アレルギー学
- 免疫学
- 微生物学(医療)
- 感染症
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