Bacterial Surface Appendages Modulate the Antimicrobial Activity Induced by Nanoflake Surfaces on Titanium

Xiayi Liu, Mohd I. Ishak, Huan Ma, Bo Su*, Angela H. Nobbs*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

3 Citations (Scopus)

Abstract

Bioinspired nanotopography is a promising approach to generate antimicrobial surfaces to combat implant-associated infection. Despite efforts to develop bactericidal 1D structures, the antibacterial capacity of 2D structures and their mechanism of action remains uncertain. Here, hydrothermal synthesis is utilized to generate two 2D nanoflake surfaces on titanium (Ti) substrates and investigate the physiological effects of nanoflakes on bacteria. The nanoflakes impair the attachment and growth of Escherichia coli and trigger the accumulation of intracellular reactive oxygen species (ROS), potentially contributing to the killing of adherent bacteria. E. coli surface appendages type-1 fimbriae and flagella are not implicated in the nanoflake-mediated modulation of bacterial attachment but do influence the bactericidal effects of nanoflakes. An E. coli ΔfimA mutant lacking type-1 fimbriae is more susceptible to the bactericidal effects of nanoflakes than the parent strain, while E. coli cells lacking flagella (ΔfliC) are more resistant. The results suggest that type-1 fimbriae confer a cushioning effect that protects bacteria upon initial contact with the nanoflake surface, while flagella-mediated motility can lead to elevated membrane abrasion. This finding offers a better understanding of the antibacterial properties of nanoflake structures that can be applied to the design of antimicrobial surfaces for future medical applications.
Original languageEnglish
Article number2310149
JournalSmall
Volume20
Issue number26
Early online date17 Jan 2024
DOIs
Publication statusE-pub ahead of print - 17 Jan 2024

Bibliographical note

Funding Information:
The authors acknowledge funding from the MRC (MR/S010343/1) and EU (BioTUNE). Bio‐TUNE project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska‐Curie grant agreement no. 872869. The authors thank Wolfson Bioimaging Facility at the University of Bristol for their help with electron microscopy. The authors thank G. Robinson (University of Kent) for kindly providing the Keio collection strains. The authors thank J‐C. Eloi at the University of Bristol for his help with TEM.

Publisher Copyright:
© 2024 The Authors. Small published by Wiley-VCH GmbH.

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