Artificial Phages with Biocatalytic Spikes for Synergistically Eradicating Antibiotic‐Resistant Biofilms

Author:

Xiao Sutong1ORCID,Xie Lan1ORCID,Gao Yang1,Wang Mao1,Geng Wei1,Wu Xizheng2,Rodriguez Raul D.3ORCID,Cheng Liang4,Qiu Li1ORCID,Cheng Chong15

Affiliation:

1. College of Polymer Science and Engineering State Key Laboratory of Polymer Materials Engineering Department of Medical Ultrasound West China Hospital Sichuan University Chengdu 610065 China

2. Max Planck Institute for Chemical Physics of Solids 01187 Dresden Germany

3. Tomsk Polytechnic University Lenin ave. 30 Tomsk 634050 Russia

4. Department of Materials Science and Engineering The Macau University of Science and Technology Taipa Macau 999078 China

5. Department of Endodontics Department of Orthodontics State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases West China Hospital of Stomatology Sichuan University Chengdu 610041 China

Abstract

AbstractAntibiotic‐resistant pathogens have become a global public health crisis, especially biofilm‐induced refractory infections. Efficient, safe, and biofilm microenvironment (BME)‐adaptive therapeutic strategies are urgently demanded to combat antibiotic‐resistant biofilms. Here, inspired by the fascinating biological structures and functions of phages, the de novo design of a spiky Ir@Co3O4 particle is proposed to serve as an artificial phage for synergistically eradicating antibiotic‐resistant Staphylococcus aureus biofilms. Benefiting from the abundant nanospikes and highly active Ir sites, the synthesized artificial phage can simultaneously achieve efficient biofilm accumulation, extracellular polymeric substance (EPS) penetration, and superior BME‐adaptive reactive oxygen species (ROS) generation, thus facilitating the in situ ROS delivery and enhancing the biofilm eradication. Moreover, transcriptomics found that the artificial phage obstructs the bacterial attachment to EPS, disrupts the maintenance of the BME, and fosters the dispersion and eradication of biofilms by down‐regulating the associated genes for the biosynthesis and preservation of both intra‐ and extracellular environments. The in vivo results demonstrate that the artificial phage can treat the biofilm‐induced recalcitrant infected wounds equivalent to vancomycin. It is suggested that the design of this spiky artificial phage with synergistic “penetrate and eradicate” capability to treat antibiotic‐resistant biofilms offers a new pathway for bionic and nonantibiotic disinfection.

Funder

National Key Research and Development Program of China

Publisher

Wiley

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