Arginine‐Enhanced Antimicrobial Activity of Nanozymes against Gram‐Negative Bacteria

Author:

Zhao Zihan12345,Wen Shu'an1234,Song Ningning6,Wang Lixiang7,Zhou Yuan1234,Deng Xue1234,Wu Changbu1234,Zhang Guili1234,Chen Jun7,Tian Guo‐Bao12348ORCID,Liang Minmin6ORCID,Zhong Lan‐Lan1234ORCID

Affiliation:

1. Program in Pathobiology The Fifth Affiliated Hospital Zhongshan School of Medicine Sun Yat‐Sen University Guangdong 510080 China

2. Advanced Medical Technology Center The First Affiliated Hospital Zhongshan School of Medicine Sun Yat‐sen University Guangzhou 510080 China

3. State Key Laboratory of Oncology in South China Sun Yat‐sen University Cancer Center Guangzhou 510060 P. R. China

4. Key Laboratory of Tropical Diseases Control (Sun Yat‐sen University) Ministry of Education Guangzhou 510080 China

5. Department of Clinical Laboratory Shenzhen People' s Hospital (Second Clinical Medical College Jinan University; The First Affiliated Hospital Southern University of Science and Technology) Shenzhen 518020 China

6. Experimental Center of Advanced Materials School of Materials Science & Engineering Beijing Institute of Technology Beijing 100081 China

7. Department of Immunology and Microbiology Zhongshan School of Medicine Sun Yat‐sen University Guangzhou 510080 China

8. Department of Immunology School of Medicine Sun Yat‐Sen University Shenzhen 518107 China

Abstract

AbstractThe continuous reduction of clinically available antibiotics has made it imperative to exploit more effective antimicrobial therapies, especially for difficult‐to‐treat Gram‐negative pathogens. Herein, it is shown that the combination of an antimicrobial nanozyme with the clinically compatible basic amino acid L‐arginine affords a potent treatment for infections with Gram‐negative pathogens. In particular, the antimicrobial activity of the antimicrobial nanozyme is dramatically increased by ≈1000‐fold after L‐arginine stimulation. Specifically, the combination therapy enhances bacterial outer and inner membrane permeability and promotes intracellular reactive oxygen species (ROS) generation. Moreover, the metabolomic and transcriptomic results reveal that combination treatment leads to the increased ROS‐mediated damage by inhibiting the tricarboxylic acid cycle and oxidative phosphorylation, thereby inducing an imbalance of the antioxidant and oxidant systems. Importantly, L‐arginine dramatically significantly accelerates the healing of infected wounds in mouse models of multidrug‐resistant peritonitis‐sepsis and skin wound infection. Overall, this work demonstrates a novel synergistic antibacterial strategy by combining the antimicrobial nanozymes with L‐arginine, which substantively facilitates the nanozyme‐mediated killing of pathogens by promoting ROS production.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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