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美罗培南、黏菌素、替加环素、利福平、头孢他啶/他唑巴坦联合对碳青霉烯类耐药鲍曼不动杆菌的体外协同抗菌活性。

In vitro synergistic antimicrobial activity of a combination of meropenem, colistin, tigecycline, rifampin, and ceftolozane/tazobactam against carbapenem-resistant Acinetobacter baumannii.

机构信息

Institute of Emerging Infectious Diseases, Korea University College of Medicine, Seoul, Republic of Korea.

Department of Physiology, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

Sci Rep. 2022 May 9;12(1):7541. doi: 10.1038/s41598-022-11464-6.

Abstract

We investigated the in vitro activity of various antimicrobial combinations against carbapenem-resistant Acinetobacter baumannii (CRAB) isolates. The in vitro activity of six two-drug combinations against CRAB isolates collected from the blood samples of patients with bloodstream infection was evaluated using the checkerboard method and time-kill assay [0.5 ×, 1 ×, and 2 × minimum inhibitory concentration (MIC)] to identify potential synergistic and bactericidal two-drug combinations against CRAB isolates. The effects of meropenem, colistin, tigecycline, rifampin, and ceftolozane/tazobactam combinations were investigated. All 10 CRAB isolates in our study produced the OXA-58-type and OXA-23-type carbapenem-hydrolyzing oxacillinases. The colistin-ceftolozane/tazobactam combination showed synergistic effects in both the time-kill assay (using an antibiotic concentration of 1 × MIC) and the checkerboard method. It also showed bactericidal effects in the time-kill assay. For all 10 CRAB isolates, time-kill curves showed synergistic bactericidal activity of the colistin-ceftolozane/tazobactam combination at 0.5 × MIC. Overall, there was substantial discordance of synergistic activity between the checkerboard microdilution and time-kill assays (with a concordance of 31.7%). Our study demonstrated that two-drug combinations of colistin and ceftolozane/tazobactam could be useful treatment alternatives for CRAB infections. The effects of these antibiotic combinations should be evaluated using in vivo experimental models.

摘要

我们研究了各种抗菌药物组合对耐碳青霉烯鲍曼不动杆菌(CRAB)分离株的体外活性。采用棋盘微量稀释法和时间杀伤试验(0.5×、1×和 2×最低抑菌浓度 [MIC])评估了 6 种二联药物组合对血流感染患者血液样本中分离的 CRAB 分离株的体外活性,以确定针对 CRAB 分离株的潜在协同和杀菌性二联药物组合。研究了美罗培南、多粘菌素、替加环素、利福平以及头孢他啶/他唑巴坦组合的效果。我们研究中的所有 10 株 CRAB 分离株均产生了 OXA-58 型和 OXA-23 型碳青霉烯水解型青霉素酶。多粘菌素-头孢他啶/他唑巴坦组合在时间杀伤试验(使用 1×MIC 的抗生素浓度)和棋盘微量稀释法中均表现出协同作用。它在时间杀伤试验中也表现出杀菌作用。对于所有 10 株 CRAB 分离株,时间杀伤曲线显示在 0.5×MIC 时多粘菌素-头孢他啶/他唑巴坦组合具有协同杀菌活性。总的来说,棋盘微量稀释法和时间杀伤试验的协同活性存在很大差异(一致性为 31.7%)。我们的研究表明,多粘菌素和头孢他啶/他唑巴坦的二联药物组合可能是治疗 CRAB 感染的有用替代方法。这些抗生素组合的效果应通过体内实验模型进行评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bb8/9085847/e859ad900b9c/41598_2022_11464_Fig1_HTML.jpg

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