Hirakawa Hidetada, Kurabayashi Kumiko, Tanimoto Koichi, Tomita Haruyoshi
Department of Bacteriology, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Laboratory of Bacterial Drug Resistance, Graduate School of Medicine, Gunma University, Maebashi, Japan.
Front Microbiol. 2018 Aug 21;9:1950. doi: 10.3389/fmicb.2018.01950. eCollection 2018.
Fosfomycin is resurfacing as a "last resort drug" to treat infections caused by multidrug resistant pathogens. This drug has a remarkable benefit in that its activity increases under oxygen-limited conditions unlike other commonly used antimicrobials such as β-lactams, fluoroquinolones and aminoglycosides. Especially, utility of fosfomycin has being evaluated with particular interest to treat chronic biofilm infections caused by because it often encounters anaerobic situations. Here, we showed that PAO1, commonly used in many laboratories, becomes more susceptible to fosfomycin when grown anaerobically, and studied on how fosfomycin increases its activity under anaerobic conditions. Results of transport assay and gene expression study indicated that PAO1 cells grown anaerobically exhibit a higher expression of encoding a glycerol-3-phosphate transporter which is responsible for fosfomycin uptake, then lead to increased intracellular accumulation of the drug. Elevated expression of in anaerobic cultures depended on ANR, a transcriptional regulator that is activated under anaerobic conditions. Purified ANR protein bound to the DNA fragment from region upstream, suggesting it is an activator of gene expression. We found that increased susceptibility to fosfomycin was also observed in a clinical isolate which has a promoted biofilm phenotype and its and genes are highly conserved with those of PAO1. We conclude that increased antibacterial activity of fosfomycin to under anaerobic conditions is attributed to elevated expression of GlpT following activation of ANR, then leads to increased uptake of the drug.
磷霉素正作为一种“最后手段药物”重新出现,用于治疗由多重耐药病原体引起的感染。这种药物有一个显著的优点,即与其他常用抗菌药物如β-内酰胺类、氟喹诺酮类和氨基糖苷类不同,它在氧气受限的条件下活性会增加。特别是,由于磷霉素经常遇到厌氧情况,其在治疗由[具体病原体]引起的慢性生物膜感染方面的效用受到了特别关注。在这里,我们发现许多实验室常用的PAO1在厌氧生长时对磷霉素更敏感,并研究了磷霉素在厌氧条件下如何增加其活性。转运测定和基因表达研究结果表明,厌氧生长的PAO1细胞表现出编码甘油-3-磷酸转运蛋白(负责磷霉素摄取)的基因更高的表达,进而导致药物在细胞内的积累增加。厌氧培养中该基因表达的升高依赖于ANR,一种在厌氧条件下被激活的转录调节因子。纯化的ANR蛋白与上游[具体基因]区域的DNA片段结合,表明它是该基因表达的激活剂。我们发现,在一种具有增强生物膜表型且其[相关基因]与PAO1的基因高度保守的临床分离株中也观察到对磷霉素的敏感性增加。我们得出结论,磷霉素在厌氧条件下对[具体病原体]抗菌活性的增加归因于ANR激活后GlpT表达的升高,进而导致药物摄取增加。