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For addressing the ever increasing challenge of multidrug-resistant (MDR) bacterial infections, specifically designed and prepared carbon dots (CDots) of small carbon nanoparticles with surface functionalization–passivation by oligomeric polyethylenimine were found to be readily activated by visible light to effectively and efficiently inactivate MDR bacterial strains. The inactivation was evaluated under various combinations of experimental conditions (dot concentrations, light intensities, and treatment times), with the results collectively suggesting CDots as a new class of promising agents for combating MDR bacteria. Mechanistic origins and implications of the observed strong antibacterial actions as relevant to the photoexcited state processes in CDots and the photodynamically induced cellular damages leading to the death of the bacterial cells were explored, with the results discussed.
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Photoactivated carbon dots inducing bacterial functional and molecular alterations
Carbon dots (CDots) of small carbon nanoparticles with oligomeric polyethylenimine for surface functionalization, coupled with visible light exposure, were found highly effective in the inactivation of bacterial pathogens. In this study, using a representative strain of a major foodborne pathogen – Listeria monocytogenes , as a target, the effects of the CDots treatment at sublethal concentrations on bacterial functions/behaviors related to the biofilm formation ability/potential, including cell attachment and swimming motility, were assessed. On the consequence at molecular level, the expression levels of the genes that are related to cell attachment/adhesion, motility, flagellar synthesis, quorum sensing, and environmental stress response and virulence were found all being up-regulated.
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- PAR ID:
- 10346233
- Date Published:
- Journal Name:
- Materials Advances
- Volume:
- 3
- Issue:
- 15
- ISSN:
- 2633-5409
- Page Range / eLocation ID:
- 6253 to 6261
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/D2MA00403H
