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Enhancing Antimicrobial Efficacy Against Pseudomonas Aeruginosa Biofilm Through Carbon Dot-mediated Photodynamic Inactivation

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Journal AMB Express
Date 2024 Sep 28
PMID 39342036
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Abstract

Pseudomonas aeruginosa biofilms shield the bacteria from antibiotics and the body's defenses, often leading to chronic infections that are challenging to treat. This study aimed to assess the impact of sub-lethal doses of antimicrobial photodynamic inactivation (sAPDI) utilizing carbon dots (CDs) derived from gentamicin and imipenem on biofilm formation and the expression of genes (pelA and pslA) associated with P. aeruginosa biofilm formation.The anti-biofilm effects of sAPDI were evaluated by exposing P. aeruginosa to sub-minimum biofilm inhibitory concentrations (sub-MBIC) of CDsGEN-NH, CDsIMP-NH, CDsGEN-IMP, and CDsIMP-GEN, combined with sub-lethal UVA light irradiation. Biofilm formation ability was assessed by crystal violet (CV) assay and enumeration method. Additionally, the impact of sAPDI on the expression of pelF and pslA genes was evaluated using real-time quantitative polymerase chain reaction (RT-qPCR).Compared to the control group, the sAPDI treatment with CDsGEN-NH, CDsIMP-NH, CDsGEN-IMP, and CDsIMP-GEN resulted in a significant reduction in biofilm activity of P. aeruginosa ATCC 27853 (P < 0.0001). The CV assay method demonstrated reductions in optical density of 83.70%, 81.08%, 89.33%, and 75.71%, while the CFU counting method showed reductions of 4.03, 3.76, 4.39, and 3.21 Log CFU/mL. qRT-PCR analysis revealed decreased expression of the pelA and pslA genes in P. aeruginosa ATCC 27853 following sAPDI treatment compared to the control group (P < 0.05).The results indicate that sAPDI using CDs derived from gentamicin and imipenem can decrease the biofilm formation of P. aeruginosa and the expression of the pelA and pslA genes associated with its biofilm formation.

References
1.
Hu X, Huang Y, Wang Y, Wang X, Hamblin M . Antimicrobial Photodynamic Therapy to Control Clinically Relevant Biofilm Infections. Front Microbiol. 2018; 9:1299. PMC: 6030385. DOI: 10.3389/fmicb.2018.01299. View

2.
Markovic Z, Kovacova M, Humpolicek P, Budimir M, Vajdak J, Kubat P . Antibacterial photodynamic activity of carbon quantum dots/polydimethylsiloxane nanocomposites against Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae. Photodiagnosis Photodyn Ther. 2019; 26:342-349. DOI: 10.1016/j.pdpdt.2019.04.019. View

3.
Schmittgen T, Livak K . Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008; 3(6):1101-8. DOI: 10.1038/nprot.2008.73. View

4.
Anand A, Unnikrishnan B, Wei S, Chou C, Zhang L, Huang C . Graphene oxide and carbon dots as broad-spectrum antimicrobial agents - a minireview. Nanoscale Horiz. 2020; 4(1):117-137. DOI: 10.1039/c8nh00174j. View

5.
Zhang J, Liu X, Wang X, Mu L, Yuan M, Liu B . Carbon dots-decorated NaWO composite with WO for highly efficient photocatalytic antibacterial activity. J Hazard Mater. 2018; 359:1-8. DOI: 10.1016/j.jhazmat.2018.06.072. View