3D bioprinting of mature bacterial biofilms for antimicrobial resistance drug testing

被引:66
作者
Ning, Evita [1 ]
Turnbull, Gareth [2 ,3 ]
Clarke, Jon [3 ]
Picard, Fred [2 ,3 ]
Riches, Philip [2 ]
Vendrell, Marc [4 ]
Graham, Duncan [1 ]
Wark, Alastair W. [1 ]
Faulds, Karen [1 ]
Shu, Wenmiao [3 ]
机构
[1] Univ Strathclyde, Technol & Innovat Ctr, Dept Pure & Appl Chem, Ctr Mol Nanometrol, 99 George St, Glasgow G1 1RD, Lanark, Scotland
[2] Univ Strathclyde, Dept Biomed Engn, 50 George St, Glasgow G1 1QE, Lanark, Scotland
[3] Golden Jubilee Natl Hosp, Dept Orthopaed, Agamemnon St, Clydebank G81 4DY, Scotland
[4] Univ Edinburgh, Med Res Council, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
3D bioprinting; biofilm; antimicrobial resistance; drug testing; STAPHYLOCOCCUS-AUREUS BACTEREMIA; PSEUDOMONAS-AERUGINOSA; IN-VITRO; CELLS; SUSCEPTIBILITY; TECHNOLOGY;
D O I
10.1088/1758-5090/ab37a0
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The potential to bioprint and study 3D bacterial biofilm constructs could have great clinical significance at a time when antimicrobial resistance is rising to dangerously high levels worldwide. In this study, clinically relevant bacterial species including Escherichia coli, Staphylococcus aureus (MSSA), Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa were 3D bioprinted using a double-crosslinked alginate bioink to form mature bacteria biofilms, characterized by confocal laser scanning microscopy (CLSM) and fluorescent staining. Solid and porous bacteria-laden constructs were reproducibly bioprinted with thicknesses ranging from 0.25 to 4 mm. We demonstrated 3D bioprinting of thicker biofilms (>4 mm) than found in currently available in vitro models. Bacterial viability was excellent in the bioprinted constructs, with CLSM observation of bacterial biofilm production and maturation possible for at least 28 d in culture. Importantly, we observed the complete five-step biofilm life cycle in vitro following 3D bioprinting for the first time, suggesting the formation of mature 3D bioprinted biofilms. Bacterial growth was faster in thinner, more porous constructs whilst constructs crosslinked with BaCl2 concentrations of above 10 mM had denser biofilm formation. 3D MRSA and MSSA biofilm constructs were found to show greater resistance to antimicrobials than corresponding two-dimensional (2D) cultures. Thicker 3D E. coli biofilms had greater resistance to tetracycline than thinner constructs over 7 d of treatment. Our methodology allowed for the precise 3D bioprinting of self-supporting 3D bacterial biofilm structures that developed biofilms during extended culture. 3D biofilm constructs containing bacterial biofilms produce a model with much greater clinical relevance compared to 2D culture models and we have demonstrated their use in antimicrobial testing.
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页数:12
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