LAUSR

Drug-resistant bacteria and biofilm-associated infections are prominent problems in the field of antibacterial medicine, seriously affecting human and animal health. Despite the great potential of nanomaterials in the antibacterial field, overcoming the paradox of size and charge, efficient penetration, and retention within biofilms remain a formidable challenge. Here, we designed self-assembling chimeric peptide nano-assemblies composed of multiple functional fragments for the treatment of drug-resistant bacteria and biofilm-associated infections. Notably, the chimeric peptide self-assembling into nanofibers at pH 7.4, transformable into nanoparticles in the acidic biofilm-infected microenvironment at pH 5.0, thus achieving a size reduction and charge increase, improving the penetration into the bacterial biofilms, and killing drug-resistant bacteria by a mechanism dominated by membrane cleavage. In vivo mouse and piglet infection models confirm the ability of chimeric peptide nano-assemblies to reduce bacterial load within biofilms. Collectively, this research on pathological environment-driven nano-structural transformations may provide a theoretical basis for designing high-performance antibacterial nanomaterials and advance the application of peptide-based nanomaterials in medicine and animal husbandry. This article is protected by copyright. All rights reserved.