Poilvache Hervé, Ruiz-Sorribas Albert, Cornu Olivier, Van Bambeke Françoise
Université catholique de Louvain, Institut de Recherche Expérimentale et Clinique, Neuromusculoskeletal Laboratory, Brussels, Belgium.
Université catholique de Louvain, Louvain Drug Research Institute, Pharmacologie cellulaire et moléculaire, Brussels, Belgium.
Antimicrob Agents Chemother. 2021 Mar 18;65(4). doi: 10.1128/AAC.01699-20.
Prosthetic joint infections (PJI) are frequent complications of arthroplasties. Their treatment is made complex by the rapid formation of bacterial biofilms, limiting the effectiveness of antibiotic therapy. In this study, we explore the effect of a tri-enzymatic cocktail (TEC) consisting of an endo-1,4-β-d-glucanase, a β-1,6-hexosaminidase, and an RNA/DNA nonspecific endonuclease combined with antibiotics of different classes against biofilms of , , and grown on Ti-6Al-4V substrates. Biofilms were grown in Trypticase soy broth (TSB) with 10 g/liter glucose and 20 g/liter NaCl (TGN). Mature biofilms were assigned to a control group or treated with the TEC for 30 min and then either analyzed or reincubated for 24 h in TGN or TGN with antibiotics. The cytotoxicity of the TEC was assayed against MG-63 osteoblasts, primary murine fibroblasts, and J-774 macrophages using the lactate dehydrogenase (LDH) release test. The TEC dispersed 80.3 to 95.2% of the biofilms' biomass after 30 min. The reincubation of the treated biofilms with antibiotics resulted in a synergistic reduction of the total culturable bacterial count (CFU) compared to that of biofilms treated with antibiotics alone in the three tested species (additional reduction from 2 to more than 3 log CFU). No toxicity of the TEC was observed against the tested cell lines after 24 h of incubation. The combination of pretreatment with TEC followed by 24 h of incubation with antibiotics had a synergistic effect against biofilms of , , and Further studies should assess the potential of the TEC as an adjuvant therapy in models of PJI.
人工关节感染(PJI)是关节置换术常见的并发症。细菌生物膜的快速形成使它们的治疗变得复杂,限制了抗生素治疗的效果。在本研究中,我们探究了一种由内切-1,4-β-D-葡聚糖酶、β-1,6-己糖胺酶和RNA/DNA非特异性内切核酸酶组成的三酶混合物(TEC)与不同类别的抗生素联合使用,对在Ti-6Al-4V基底上生长的金黄色葡萄球菌、表皮葡萄球菌和粪肠球菌生物膜的影响。生物膜在含有10 g/升葡萄糖和20 g/升氯化钠的胰蛋白酶大豆肉汤(TSB)(TGN)中生长。成熟生物膜被分为对照组,或用TEC处理30分钟,然后进行分析,或在TGN或含抗生素的TGN中再孵育24小时。使用乳酸脱氢酶(LDH)释放试验测定TEC对MG-63成骨细胞、原代小鼠成纤维细胞和J-774巨噬细胞的细胞毒性。30分钟后,TEC分散了80.3%至95.2%的生物膜生物量。与单独用抗生素处理的生物膜相比,用抗生素对处理后的生物膜进行再孵育,在三种受试菌种中导致可培养细菌总数(CFU)协同减少(额外减少2至超过3个对数CFU)。孵育24小时后,未观察到TEC对受试细胞系有毒性。先用TEC预处理,然后用抗生素孵育24小时的联合处理对金黄色葡萄球菌、表皮葡萄球菌和粪肠球菌生物膜具有协同作用。进一步的研究应评估TEC作为PJI模型辅助治疗的潜力。