Bacterial Infections: Antimicrobial Therapies group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Microbiology Section, Department of Genetics, Microbiology, and Statistics, Biology Faculty, Universitat de Barcelona, Barcelona, Spain.
NPJ Biofilms Microbiomes. 2022 Jul 4;8(1):52. doi: 10.1038/s41522-022-00317-9.
The extracellular matrix protects biofilm cells by reducing diffusion of antimicrobials. Tobramycin is an antibiotic used extensively to treat P. aeruginosa biofilms, but it is sequestered in the biofilm periphery by the extracellular negative charge matrix and loses its efficacy significantly. Dispersal of the biofilm extracellular matrix with enzymes such as DNase I is another promising therapy that enhances antibiotic diffusion into the biofilm. Here, we combine the charge neutralization of tobramycin provided by dextran-based single-chain polymer nanoparticles (SCPNs) together with DNase I to break the biofilm matrix. Our study demonstrates that the SCPNs improve the activity of tobramycin and DNase I by neutralizing the ionic interactions that keep this antibiotic in the biofilm periphery. Moreover, the detailed effects and interactions of nanoformulations with extracellular matrix components were revealed through time-lapse imaging of the P. aeruginosa biofilms by laser scanning confocal microscopy with specific labeling of the different biofilm components.
细胞外基质通过减少抗菌药物的扩散来保护生物膜细胞。妥布霉素是一种广泛用于治疗铜绿假单胞菌生物膜的抗生素,但它被细胞外负电荷基质隔离在生物膜的外围,从而显著降低了其疗效。用酶(如 DNA 酶 I)分散生物膜细胞外基质是另一种有前途的治疗方法,它可以增强抗生素向生物膜内部的扩散。在这里,我们将基于葡聚糖的单链聚合物纳米粒子 (SCPN) 提供的妥布霉素电荷中和作用与 DNA 酶 I 结合起来,以破坏生物膜基质。我们的研究表明,SCPN 通过中和将这种抗生素保留在生物膜外围的离子相互作用,提高了妥布霉素和 DNA 酶 I 的活性。此外,通过激光扫描共聚焦显微镜对铜绿假单胞菌生物膜进行特定标记,对不同生物膜成分进行时程成像,揭示了纳米制剂与细胞外基质成分的详细作用和相互作用。