| Literature DB >> 33278958 |
Haitao Yu1, Zhengxin Ma2, Shanyu Meng3, Shiyan Qiao4, Xiangfang Zeng4, Zhaohui Tong3, Kwangcheol Casey Jeong5.
Abstract
Bacterial resistance to antibiotics is a critical public health concern. Alternatives of antibiotics are needed urgently. Herein, we designed and engineered a new nano-antimicrobial, chitosan nanoparticles (CNs)-antimicrobial peptide microcin J25 (MccJ25) conjugates (CNMs). The engineered CNMs proved to be highly active against Gram-negative and Gram-positive bacteria, and the activity of CNMs and CNs was stable in various thermal and pH environments. Escherichia coli K88 strain treated with CNMs did not acquire resistance in serial passage assays over a period of 18 days. Risk assessment with cell lines showed that CNMs did not cause toxicity. Additionally, CNMs did not reduce the lifespan of C. elegans. In summary, this study demonstrated that CNMs can serve as an excellent novel antimicrobial agent against multi-drug resistance pathogens.Entities:
Keywords: Antimicrobial activity; Antimicrobial peptide microcin J25; Caenorhabditis elegans; Chitosan nanoparticles; Mutagenesis; Toxicity
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Year: 2020 PMID: 33278958 DOI: 10.1016/j.carbpol.2020.117309
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381