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

被引:33
|
作者
Liu, Danqing [1 ,2 ]
Xi, Yuejing [2 ]
Yu, Shunzhi [1 ]
Yang, Kexin [2 ]
Zhang, Fan [3 ,4 ]
Yang, Yuying [2 ]
Wang, Tianlong [1 ]
He, Shisheng [1 ]
Zhu, Yunqing [1 ,2 ]
Fan, Zhen [1 ,2 ]
Du, Jianzhong [1 ,2 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, Dept Orthoped, Shanghai 200072, Peoples R China
[2] Tongji Univ, Sch Mat Sci & Engn, Dept Polymer Mat, 4800 Caoan Rd, Shanghai 201804, Peoples R China
[3] Tongji Univ, Shanghai Res Ctr Tooth Restorat & Regenerat, Stomatol Hosp, Dept Oral Implantol, Shanghai 200072, Peoples R China
[4] Tongji Univ, Shanghai Res Ctr Tooth Restorat & Regenerat, Dent Sch, Shanghai 200072, Peoples R China
基金
上海市自然科学基金;
关键词
Orthopedic implants; Biofilm; Antimicrobial resistance; Polypeptides; Antibacterial; ANTIMICROBIAL PEPTIDES; STAPHYLOCOCCUS-AUREUS; SURFACES; INFECTIONS; PROTEINS; ADHESION; ACIDS;
D O I
10.1016/j.biomaterials.2022.121957
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页数:13
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