Tan Xin, Coureuil Mathieu, Ramond Elodie, Euphrasie Daniel, Dupuis Marion, Tros Fabiola, Meyer Julie, Nemazanyy Ivan, Chhuon Cerina, Guerrera Ida Chiara, Ferroni Agnes, Sermet-Gaudelus Isabelle, Nassif Xavier, Charbit Alain, Jamet Anne
Université Paris Descartes, INSERM U1151 - CNRS UMR 8253, Institut Necker-Enfants Malades. Team: Pathogenesis of Systemic Infections, Paris, France.
Plateforme d'étude du métabolisme, Structure Fédérative de Recherche INSERM US24/CNRS UMS3633, Paris, France.
Clin Infect Dis. 2019 Nov 13;69(11):1937-1945. doi: 10.1093/cid/ciz106.
Chronic lung infection in cystic fibrosis (CF) patients by Staphylococcus aureus is a well-established epidemiological fact. Indeed, S. aureus is the most commonly identified pathogen in the lungs of CF patients. Improving our understanding of the mechanisms associated with the persistence of S. aureus is therefore an important issue.
We selected pairs of sequential S. aureus isolates from 3 patients with CF and from 1 patient with non-CF chronic lung disease. We used a combination of genomic, proteomic, and metabolomic approaches with functional assays for in-depth characterization of S. aureus long-term persistence.
In this study, we show that late S. aureus isolates from CF patients have an increased ability for intracellular survival in CF bronchial epithelial-F508del cells compared to ancestral early isolates. Importantly, the increased ability to persist intracellularly was confirmed for S. aureus isolates within the own-patient F508del epithelial cells. An increased ability to form biofilm was also demonstrated. Furthermore, we identified the underlying genetic modifications that induce altered protein expression profiles and notable metabolic changes. These modifications affect several metabolic pathways and virulence regulators that could constitute therapeutic targets.
Our results strongly suggest that the intracellular environment might constitute an important niche of persistence and relapse necessitating adapted antibiotic treatments.
金黄色葡萄球菌对囊性纤维化(CF)患者造成慢性肺部感染是一个已被充分证实的流行病学事实。事实上,金黄色葡萄球菌是CF患者肺部最常鉴定出的病原体。因此,加深我们对与金黄色葡萄球菌持续存在相关机制的理解是一个重要问题。
我们从3例CF患者和1例非CF慢性肺部疾病患者中选取了成对的连续金黄色葡萄球菌分离株。我们结合了基因组学、蛋白质组学和代谢组学方法以及功能测定,以深入表征金黄色葡萄球菌的长期持续性。
在本研究中,我们发现与原始早期分离株相比,CF患者的晚期金黄色葡萄球菌分离株在CF支气管上皮-F508del细胞中的细胞内存活能力增强。重要的是,在患者自身的F508del上皮细胞内,金黄色葡萄球菌分离株的细胞内持续存在能力增强也得到了证实。还证明了其形成生物膜的能力增强。此外,我们确定了导致蛋白质表达谱改变和显著代谢变化的潜在基因修饰。这些修饰影响了几个可能构成治疗靶点的代谢途径和毒力调节因子。
我们的结果强烈表明,细胞内环境可能是持续性和复发的重要生态位,需要采用适应性抗生素治疗。