多种抗生素对囊性纤维化患者分离的木氧化无色杆菌菌株的抗生素后效应

Berna Özbek-Çelik, Damla Damar-Çelik, N. Nørskov-Lauritsen
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引用次数: 0

摘要

目的:木氧化无色杆菌是囊性纤维化(CF)疾病中一种新出现的病原体,尽管其临床影响和最佳治疗方法相对有限。抗生素后效应(PAE)等药效学正越来越多地应用于抗生素给药方案的设计。本研究对美罗培南、多里培烯、粘菌素、左氧氟沙星、替加环素、妥布霉素和氯霉素的PAE进行了检测。为了测定PAEs,将处于对数生长期的木糖氧化酶菌株暴露于抗生素1小时。离心后使用活细胞计数评估试验培养物的回收期。结果:粘菌素在1xMIC和4xMIC浓度下的体外PAEs平均值分别为3.21±0.66和3.58±0.68小时,左氧氟沙星为1.54±0.46和2.27±0.41小时,妥布霉素为2.34±0.48和3.47±0.64小时,替加环素为1.72±0.47和2.24±0.41 h,氯霉素为1.91±0.14和2.13±0.13小时。正如预期的那样,碳青霉烯类抗生素表现出较弱的PAE。结论:这项研究的发现可能对测试抗生素的抗菌治疗中的剂量选择具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-antibiotic Effect of Various Antibiotics against Achromobacter xylosoxidans Strains Isolated from Patients with Cystic Fibrosis
Objectives: Achromobacter xylosoxidans is an emerging pathogen in cystic fibrosis (CF) disease, although relatively limited is known about its clinical impact and optimal management. Pharmacodynamics such as post-antibiotic effect (PAE) are increasingly being applied to the design of antibiotic dosing regimens. In the present study, meropenem, doripenem, colistin, levofloxacin, tigecycline, tobramycin, and chloramphenicol were tested for their PAE. Materials and Methods: The in vitro activities of meropenem, doripenem, colistin, levofloxacin, tigecycline, tobramycin, and chloramphenicol were determined by the microbroth dilution technique. To determine the PAEs, A. xylosoxidans strains in the logarithmic phase of growth were exposed for 1 h to antibiotics. Recovery periods of test cultures were evaluated using viable counting after centrifugation. Results: The mean values of in vitro PAEs at 1xMIC and 4xMIC concentrations were 3.21 ± 0.66 and 3.58 ± 0.68 hours for colistin, 1.54 ± 0.46 and 2.27 ± 0.41 hours for levofloxacin, 2.34 ± 0.48 and 3.47 ± 0.64 hours for tobramycin, 1.72 ± 0.47 and 2.24 ± 0.41 hours for tigecycline 1.91 ± 0.14 and 2.13 ± 0.13 hours for chloramphenicol, respectively. The carbapenem antibiotics exhibited weak PAEs, as expected. Conclusions: This study’s findings could have important implications for the timing of doses during antimicrobial therapy with tested antibiotics.
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