Methylene Blue–Mediated Antimicrobial ​Photodynamic Therapy Against Clinical Isolates of Extensively Drug Resistant ​Gram-Negative Bacteria Causing Nosocomial Infections in Thailand, An In Vitro Study

Acinetobacter baumannii Organic chemistry FOS: Basic medicine Multiple drug resistance Gene Biochemistry Photodynamic therapy Cellular and Infection Microbiology Engineering Anti-Infective Agents Antibiotics Cross Infection 0303 health sciences methylene blue (MB) Acinetobacter Colony-forming unit Multidrug-Resistant Bacteria Life Sciences Thailand QR1-502 Anti-Bacterial Agents 3. Good health Klebsiella pneumoniae Chemistry photodynamic therapy nosocomial infection Physical Sciences Photodynamic Therapy Pseudomonas aeruginosa Medicine Molecular Medicine Paper-Based Diagnostic Devices Pulmonary and Respiratory Medicine Photodynamic Therapy in Oncology and Microbiology Biomedical Engineering FOS: Medical engineering Microbiology antimicrobials Catalysis Global Challenge of Antibiotic Resistance in Bacteria 03 medical and health sciences Biochemistry, Genetics and Molecular Biology Gram-Negative Bacteria Health Sciences Escherichia coli Genetics Humans Photocatalysis Biology Methylene blue Bacteria Methylene Blue Photochemotherapy FOS: Biological sciences Drug resistance Antimicrobial multidrug resistance (MDR)
DOI: 10.3389/fcimb.2022.929242 Publication Date: 2022-07-01T05:43:42Z
ABSTRACT
Background/PurposeSome multidrug-resistant gram-negative bacteria as a global threat have been recently prioritized for research and development of new treatments. We studied the efficacy of methylene blue–mediated antimicrobial photodynamic therapy (MB-aPDT) for the reduction of extensively drug-resistant Acinetobacter baumannii (XDR-AB) and Pseudomonas aeruginosa (XDR-PS) and multidrug-resistant Klebsiella pneumoniae (MDR-KP) isolated in a university hospital setting in Thailand.MethodTwo isolates of each selected bacterium were collected, XDR-AB1 and AB2, XDR- PS1 and PS2, and MDR-KP1 and KP2. Three triplicate experiments using various MB concentrations alone, various red light fluences alone, as well as the selected non-toxic doses of MB and fluences of red light combined as MB-aPDT were applied on each selected isolate. The colonies were counted [colony forming units (CFU)/ml]. Estimation of the lethal treatment dose defined as reduction of > 2 log10 in CFU/ml compared with untreated bacteria.ResultThere were generally negligible changes in the viable counts of the bacterial suspensions treated with all the MB concentrations (p > 0.05). In the second experiment with the only red light treatments, at fluences higher than 2 J/cm, reduction trend in viable counts across all the isolates was observed. Only for MDR-KP1, however, the lethal dose was achieved with the highest fluence of red light (80 J/cm). With the concentration of MB, 50 and 150 mg/L in the third experiment (MB-aPDT), the greater bacterial reduction was observed in all clinical isolates leading to their lethal viable cell reduction when escalating the light fluence to 80 J/cm.ConclusionsMB-aPDT evidently killed the selected XDR and MDR-gram negative bacteria. In highly drug-resistant crisis era, MB-aPDT could be a promising option, particularly for local infections and infection complicating chronic wounds.
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