4.8 Article

A polypeptide coating for preventing biofilm on implants by inhibiting antibiotic resistance genes

期刊

BIOMATERIALS
卷 293, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2022.121957

关键词

Orthopedic implants; Biofilm; Antimicrobial resistance; Polypeptides; Antibacterial

向作者/读者索取更多资源

Aging population has increased the demand for orthopedic implants. However, biofilm formation on implants due to antibiotic insensitivity and antimicrobial resistance has been a major challenge. In this study, an antibacterial polypeptide coating was developed to prevent biofilm formation and acquired antibiotic resistance. The coating demonstrated excellent in vivo adhesive capacity and strong antibacterial activity. It also inhibited the expression of genes associated with antimicrobial resistance. In vivo experiments confirmed the effectiveness of the coating in preventing biofilm formation and infections. Overall, this study provides a simple method for preparing antibacterial orthopedic implants without inducing antimicrobial resistance.
Aging population has been boosting the need for orthopedic implants. However, biofilm has been a major obstacle for orthopedic implants due to its insensitivity to antibiotics and tendency to drive antimicrobial resistance. Herein, an antibacterial polypeptide coating with excellent in vivo adhesive capacity was prepared to prevent implants from forming biofilms and inducing acquired antibiotic resistance. A peptide-based copolymer, poly[phenylalanine10-stat-lysine12]-block-3,4-dihydroxy-L-phenylalanine [Poly(Phe10-stat-Lys12)-DOPA] was modularly designed, where poly(Phe10-stat-Lys12) is antibacterial polypeptide with high antibacterial activity, and DOPA provides strong adhesion in both wet and dry microenvironments. Meanwhile, compared to tradi-tional graft-onto methods, this antibacterial coating can be facilely achieved by immersing Titanium substrates into antibacterial polypeptide solution for 5 min at room temperature. The poly(Phe10-stat-Lys12)-DOPA polymer showed good antibacterial activity with minimum inhibitory concentrations against S. aureus and E. coli of 32 and 400 mu g/mL, respectively. Compared to obvious antimicrobial resistance of S. aureus after continuous treatment with vancomycin, this antibacterial coating doesn't drive antimicrobial resistance upon long-term utilization. Transcriptome sequencing and qPCR tests further confirmed that the antibacterial coating was able to inhibit the expression of multiple peptide resistance factor (mprF) and lipoteichoic acid modification D-alanylation genes (dltB and dltC) that can increase the net positive charge of bacterial cell wall to induce the resistance to cationic antimicrobial peptides. In vivo experiments confirmed that this poly(Phe10-stat-Lys12)-DOPA coating can both effectively prevent biofilm formation through surface contact sterilization and avoid local and systemic infections. Overall, we proposed a facile method for preparing antibacterial orthopedic im-plants with longer indwelling time and without inducing antimicrobial resistance by coating a polypeptide-based polymer on the implants.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据