Zamorano Laura, Moyà Bartolomé, Juan Carlos, Mulet Xavier, Blázquez Jesús, Oliver Antonio
Servicio de Microbiología and Unidad de Investigación, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria de Palma (IdISPa), Palma de Mallorca, Spain.
Servicio de Microbiología and Unidad de Investigación, Hospital Universitario Son Espases, Instituto de Investigación Sanitaria de Palma (IdISPa), Palma de Mallorca, Spain
Antimicrob Agents Chemother. 2014 Sep;58(9):5084-95. doi: 10.1128/AAC.02556-14. Epub 2014 Jun 16.
Pseudomonas aeruginosa is a ubiquitous versatile environmental microorganism with a remarkable ability to grow under diverse environmental conditions. Moreover, P. aeruginosa is responsible for life-threatening infections in immunocompromised and cystic fibrosis patients, as the extraordinary capacity of this pathogen to develop antimicrobial resistance dramatically limits our therapeutic arsenal. Its large genome carries an outstanding number of genes belonging to regulatory systems, including multiple two-component sensor-regulator systems that modulate the response to the different environmental stimuli. Here, we show that one of two systems, designated CreBC (carbon source responsive) and BlrAB (β-lactam resistance), might be of particular relevance. We first identified the stimuli triggering the activation of the CreBC system, which specifically responds to penicillin-binding protein 4 (PBP4) inhibition by certain β-lactam antibiotics. Second, through an analysis of a large comprehensive collection of mutants, we demonstrate an intricate interconnection between the CreBC system, the peptidoglycan recycling pathway, and the expression of the concerning chromosomal β-lactamase AmpC. Third, we show that the CreBC system, and particularly its effector inner membrane protein CreD, plays a major role in bacterial fitness and biofilm development, especially in the presence of subinhibitory concentrations of β-lactams. Finally, global transcriptomics reveals broad regulatory functions of CreBC in basic physiological aspects, particularly anaerobic respiration, in both the presence and absence of antibiotics. Therefore, the CreBC system is envisaged as a potentially interesting target for improving the efficacy of β-lactams against P. aeruginosa infections.
铜绿假单胞菌是一种普遍存在的多功能环境微生物,具有在多种环境条件下生长的显著能力。此外,铜绿假单胞菌会导致免疫功能低下和囊性纤维化患者发生危及生命的感染,因为这种病原体产生抗微生物耐药性的非凡能力极大地限制了我们的治疗手段。其庞大的基因组携带了大量属于调控系统的基因,包括多个双组分传感调节系统,这些系统可调节对不同环境刺激的反应。在此,我们表明,两个系统之一,即命名为CreBC(碳源响应)和BlrAB(β-内酰胺抗性)的系统可能具有特别重要的意义。我们首先确定了触发CreBC系统激活的刺激因素,该系统对某些β-内酰胺抗生素抑制青霉素结合蛋白4(PBP4)有特异性反应。其次,通过对大量综合突变体文库的分析,我们证明了CreBC系统、肽聚糖循环途径和相关染色体β-内酰胺酶AmpC的表达之间存在复杂的相互联系。第三,我们表明CreBC系统,尤其是其效应器内膜蛋白CreD,在细菌适应性和生物膜形成中起主要作用,特别是在存在亚抑制浓度的β-内酰胺时。最后,全局转录组学揭示了CreBC在基本生理方面,特别是在有无抗生素情况下的厌氧呼吸中的广泛调控功能。因此,CreBC系统被设想为提高β-内酰胺对铜绿假单胞菌感染疗效的一个潜在有趣靶点。