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单肟型铁载体 BAL30072 与碳青霉烯类抗生素联用对多重耐药革兰氏阴性杆菌的协同作用。

Combined effects of the siderophore monosulfactam BAL30072 and carbapenems on multidrug-resistant Gram-negative bacilli.

机构信息

Basilea Pharmaceutica International Ltd, Grenzacherstrasse 487, CH-4058 Basel, Switzerland.

出版信息

J Antimicrob Chemother. 2013 May;68(5):1120-9. doi: 10.1093/jac/dks527. Epub 2013 Jan 22.

Abstract

OBJECTIVES

Carbapenem resistance in Gram-negative bacteria, mediated by restricted net influx and carbapenem-hydrolysing β-lactamases, is a growing problem. The monosulfactam antibiotic BAL30072 is stable to most carbapenemases, suggesting that it could be complementary to carbapenems. We have investigated the antimicrobial activity of BAL30072 combined with imipenem, meropenem and doripenem.

METHODS

The in vitro activities of the combinations were evaluated using broth microdilution susceptibility and agar disc diffusion tests, broth dilution chequerboard titration and time-kill studies, using strains of Enterobacteriaceae, Pseudomonas aeruginosa and Acinetobacter with carbapenem MICs ≥ 2 mg/L.

RESULTS

The combinations were effective against 70%-80% of the isolates tested in the presence of 1 mg/L of each antibiotic, whereas the carbapenems were ineffective and BAL30072 alone was effective against 20%-40% of the strains. Synergistic effects were observed with many Enterobacteriaceae and P. aeruginosa, but were less common among the Acinetobacter, although additive effects, where the activity of one partner compensated for lack of activity of the other, were common. None of the combinations exhibited an antagonistic effect in all tests, in contrast to other β-lactams where negative interactions were frequently observed. Animal models of septicaemia demonstrated that the synergy observed in vitro with BAL30072 and meropenem can translate into greater in vivo efficacy.

CONCLUSIONS

BAL30072/carbapenem combinations were effective against a broader range of multidrug-resistant Gram-negative bacteria than either of the single agents. Additive and synergistic effects were observed in Enterobacteriaceae and P. aeruginosa, and this enhanced activity was frequently associated with suppression of resistance development. The in vitro activity translated into improved in vivo efficacy.

摘要

目的

由有限的净流入和碳青霉烯水解β-内酰胺酶介导的革兰氏阴性菌碳青霉烯耐药性是一个日益严重的问题。单磺酰胺抗生素 BAL30072 对大多数碳青霉烯酶稳定,这表明它可能与碳青霉烯互补。我们研究了 BAL30072 与亚胺培南、美罗培南和多利培南联合使用的抗菌活性。

方法

使用肉汤微量稀释药敏试验和琼脂扩散试验、肉汤稀释棋盘滴定和时间杀伤研究,评估组合的体外活性,使用碳青霉烯 MIC≥2mg/L 的肠杆菌科、铜绿假单胞菌和不动杆菌菌株。

结果

在每种抗生素 1mg/L 的存在下,组合对 70%-80%的受试分离株有效,而碳青霉烯无效,BAL30072 单独对 20%-40%的菌株有效。在许多肠杆菌科和铜绿假单胞菌中观察到协同作用,但在不动杆菌中则较少见,尽管常见的是相加作用,即一种药物的活性补偿了另一种药物的无活性。与其他β-内酰胺类药物不同,在所有试验中,这些组合都没有表现出拮抗作用,而在其他β-内酰胺类药物中,经常观察到负相互作用。败血症动物模型表明,BAL30072 和美罗培南在体外观察到的协同作用可以转化为更大的体内疗效。

结论

与单一药物相比,BAL30072/碳青霉烯类药物组合对更广泛的多药耐药革兰氏阴性菌有效。在肠杆菌科和铜绿假单胞菌中观察到相加和协同作用,这种增强的活性通常与抑制耐药性发展有关。体外活性转化为改善的体内疗效。

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