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磷霉素和妥布霉素联合下调硝酸还原酶基因 narG 和 narH,导致铜绿假单胞菌在厌氧条件下的活性增加。

Fosfomycin and tobramycin in combination downregulate nitrate reductase genes narG and narH, resulting in increased activity against Pseudomonas aeruginosa under anaerobic conditions.

机构信息

CF and Airways Microbiology Research Group, Queen's University, Belfast, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2013 Nov;57(11):5406-14. doi: 10.1128/AAC.00750-13. Epub 2013 Aug 19.

Abstract

The activity of aminoglycosides, which are used to treat Pseudomonas aeruginosa respiratory infection in cystic fibrosis (CF) patients, is reduced under the anaerobic conditions that reflect the CF lung in vivo. In contrast, a 4:1 (wt/wt) combination of fosfomycin and tobramycin (F:T), which is under investigation for use in the treatment of CF lung infection, has increased activity against P. aeruginosa under anaerobic conditions. The aim of this study was to elucidate the mechanisms underlying the increased activity of F:T under anaerobic conditions. Microarray analysis was used to identify the transcriptional basis of increased F:T activity under anaerobic conditions, and key findings were confirmed by microbiological tests, including nitrate utilization assays, growth curves, and susceptibility testing. Notably, growth in subinhibitory concentrations of F:T, but not tobramycin or fosfomycin alone, significantly downregulated (P < 0.05) nitrate reductase genes narG and narH, which are essential for normal anaerobic growth of P. aeruginosa. Under anaerobic conditions, F:T significantly decreased (P < 0.001) nitrate utilization in P. aeruginosa strains PAO1, PA14, and PA14 lasR::Gm, a mutant known to exhibit increased nitrate utilization. A similar effect was observed with two clinical P. aeruginosa isolates. Growth curves indicate that nitrate reductase transposon mutants had reduced growth under anaerobic conditions, with these mutants also having increased susceptibility to F:T compared to the wild type under similar conditions. The results of this study suggest that downregulation of nitrate reductase genes resulting in reduced nitrate utilization is the mechanism underlying the increased activity of F:T under anaerobic conditions.

摘要

氨基糖苷类抗生素用于治疗囊性纤维化(CF)患者的铜绿假单胞菌呼吸道感染,但其活性在体内 CF 肺的厌氧条件下降低。相比之下,正在研究用于治疗 CF 肺部感染的磷霉素和妥布霉素(F:T)以 4:1(重量/重量)的比例组合,在厌氧条件下对铜绿假单胞菌的活性增加。本研究旨在阐明 F:T 在厌氧条件下活性增加的机制。使用微阵列分析来确定厌氧条件下 F:T 活性增加的转录基础,并通过微生物学测试(包括硝酸盐利用测定、生长曲线和药敏试验)确认关键发现。值得注意的是,在亚抑菌浓度的 F:T 生长时,而不是单独使用妥布霉素或磷霉素,显著下调(P<0.05)铜绿假单胞菌正常厌氧生长所必需的硝酸盐还原酶基因 narG 和 narH。在厌氧条件下,F:T 显著降低(P<0.001)PAO1、PA14 和 PA14 lasR::Gm 等铜绿假单胞菌菌株的硝酸盐利用,后者是一种已知增加硝酸盐利用的突变体。在两种临床铜绿假单胞菌分离株中也观察到类似的效果。生长曲线表明,硝酸盐还原酶转座子突变体在厌氧条件下的生长减少,与野生型相比,这些突变体在类似条件下对 F:T 的敏感性也增加。本研究结果表明,硝酸盐还原酶基因下调导致硝酸盐利用减少是 F:T 在厌氧条件下活性增加的机制。

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