Leibniz Institute for Natural Product Research and Infection Biology, Hans Knöll Institute (HKI), Bio Pilot Plant, Jena, Germany ; Faculty of Physics and Astronomy, Chair of Materials Science (CMS), Friedrich Schiller University Jena, Jena, Germany.
Faculty of Physics and Astronomy, Chair of Materials Science (CMS), Friedrich Schiller University Jena, Jena, Germany.
PLoS One. 2014 Jan 3;9(1):e84837. doi: 10.1371/journal.pone.0084837. eCollection 2014.
Biomaterials-associated infections are primarily initiated by the adhesion of microorganisms on the biomaterial surfaces and subsequent biofilm formation. Understanding the fundamental microbial adhesion mechanisms and biofilm development is crucial for developing strategies to prevent such infections. Suitable in vitro systems for biofilm cultivation and bacterial adhesion at controllable, constant and reproducible conditions are indispensable. This study aimed (i) to modify the previously described constant-depth film fermenter for the reproducible cultivation of biofilms at non-depth-restricted, constant and low shear conditions and (ii) to use this system to elucidate bacterial adhesion kinetics on different biomaterials, focusing on biomaterials surface nanoroughness and hydrophobicity. Chemostat-grown Escherichia coli were used for biofilm cultivation on titanium oxide and investigating bacterial adhesion over time on titanium oxide, poly(styrene), poly(tetrafluoroethylene) and glass. Using chemostat-grown microbial cells (single-species continuous culture) minimized variations between the biofilms cultivated during different experimental runs. Bacterial adhesion on biomaterials comprised an initial lag-phase I followed by a fast adhesion phase II and a phase of saturation III. With increasing biomaterials surface nanoroughness and increasing hydrophobicity, adhesion rates increased during phases I and II. The influence of materials surface hydrophobicity seemed to exceed that of nanoroughness during the lag-phase I, whereas it was vice versa during adhesion phase II. This study introduces the non-constant-depth film fermenter in combination with a chemostat culture to allow for a controlled approach to reproducibly cultivate biofilms and to investigate bacterial adhesion kinetics at constant and low shear conditions. The findings will support developing and adequate testing of biomaterials surface modifications eventually preventing biomaterial-associated infections.
生物材料相关感染主要是由微生物在生物材料表面的黏附以及随后的生物膜形成引起的。了解微生物黏附机制和生物膜形成的基本原理对于开发预防此类感染的策略至关重要。可控、恒定和可重复的条件下培养生物膜和细菌黏附的合适体外系统是必不可少的。本研究旨在:(i)修改先前描述的恒深膜发酵器,以在不受深度限制、恒定和低剪切条件下可重复地培养生物膜;(ii)利用该系统阐明不同生物材料上细菌黏附的动力学,重点关注生物材料表面纳米粗糙度和疏水性。恒化器培养的大肠杆菌用于在氧化钛上培养生物膜,并研究氧化钛、聚苯乙烯、聚四氟乙烯和玻璃上随时间推移的细菌黏附情况。使用恒化器培养的微生物细胞(单物种连续培养)最大限度地减少了不同实验运行中培养的生物膜之间的差异。生物材料上的细菌黏附包括初始迟滞期 I,随后是快速黏附期 II 和饱和期 III。随着生物材料表面纳米粗糙度和疏水性的增加,I 期和 II 期的黏附速率增加。材料表面疏水性的影响似乎在迟滞期 I 期间超过了纳米粗糙度,而在黏附期 II 期间则相反。本研究引入了非恒深膜发酵器与恒化器培养相结合的方法,可实现可重复培养生物膜的受控方法,并在恒定和低剪切条件下研究细菌黏附动力学。这些发现将支持开发和充分测试生物材料表面改性,最终预防生物材料相关感染。