4.6 Article

Photodynamic Inactivation of E. coli Bacteria via Carbon Nanodots

Journal

ACS OMEGA
Volume 6, Issue 37, Pages 23742-23749

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c01700

Keywords

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Funding

  1. German Federal Ministry for Food and Agriculture (BMEL) [2817600712]
  2. Deutsche Forschungsgemeinschaft
  3. Open Access Publishing Fund of University of Potsdam

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The increasing antibiotic resistance in bacteria is a major problem in human and veterinary medicine. Using carbon nanodots for photodynamic inactivation is an effective method to selectively kill bacteria without damaging the cell membrane.
The increasing development of antibiotic resistance in bacteria has been a major problem for years, both in human and veterinary medicine. Prophylactic measures, such as the use of vaccines, are of great importance in reducing the use of antibiotics in livestock. These vaccines are mainly produced based on formaldehyde inactivation. However, the latter damages the recognition elements of the bacterial proteins and thus could reduce the immune response in the animal. An alternative inactivation method developed in this work is based on gentle photodynamic inactivation using carbon nanodots (CNDs) at excitation wavelengths lambda(ex) > 290 nm. The photodynamic inactivation was characterized on the nonvirulent laboratory strain Escherichia coli K12 using synthesized CNDs. For a gentle inactivation, the CNDs must be absorbed into the cytoplasm of the E. coli cell. Thus, the inactivation through photoinduced formation of reactive oxygen species only takes place inside the bacterium, which means that the outer membrane is neither damaged nor altered. The loading of the CNDs into E. coli was examined using fluorescence microscopy. Complete loading of the bacterial cells could be achieved in less than 10 min. These studies revealed a reversible uptake process allowing the recovery and reuse of the CNDs after irradiation and before the administration of the vaccine. The success of photodynamic inactivation was verified by viability assays on agar. In a homemade flow photoreactor, the fastest successful irradiation of the bacteria could be carried out in 34 s. Therefore, the photodynamic inactivation based on CNDs is very effective. The membrane integrity of the bacteria after irradiation was verified by slide agglutination and atomic force microscopy. The method developed for the laboratory strain E. coli K12 could then be successfully applied to the important avian pathogens Bordetella avium and Ornithobacterium rhinotracheale to aid the development of novel vaccines.

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