Blue Light Compromises Bacterial β-Lactamases Activity to Overcome β-Lactam Resistance.
Carolina Dos Anjos1, Yin Wang2, Que Chi Truong-Bolduc2
1Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Lasers in Surgery and Medicine
|July 23, 2024
Summary
Antimicrobial blue light (aBL) effectively kills bacteria producing β-lactamase and reduces enzyme activity. This approach shows promise for overcoming antibiotic resistance, particularly when combined with antibiotics like ceftazidime.
Area of Science:
- Photomedicine
- Antimicrobial resistance research
- Biochemistry
Background:
- β-lactamase enzymes confer resistance to β-lactam antibiotics.
- Antimicrobial blue light (aBL) is an emerging therapeutic modality.
- Investigating aBL's efficacy against resistant bacteria is crucial.
Purpose of the Study:
- To evaluate the effectiveness of antimicrobial blue light (aBL) against β-lactamase-producing bacteria.
- To determine the impact of aBL on β-lactamase activity.
- To assess the synergistic effect of aBL with ceftazidime.
Main Methods:
- Exposure of bacterial strains (P. aeruginosa, E. coli, K. pneumoniae) and purified β-lactamases to aBL (410 nm).
- Assay of β-lactamase activity using chromogenic cephalosporin hydrolysis.
- Analysis of porphyrin photoreaction and protein degradation (SDS-PAGE).
- Evaluation of combined aBL-ceftazidime treatment against a metallo-β-lactamase strain.
Main Results:
- aBL significantly reduced β-lactamase activity in bacteria and purified enzymes.
- A 50% reduction in enzymatic activity was observed in P. aeruginosa after 1.52 J/cm² aBL exposure.
- aBL induced protein degradation, contributing to reduced enzyme activity.
- Combined aBL and ceftazidime enhanced bactericidal effects by over 4-log10 against resistant P. aeruginosa.
Conclusions:
- aBL effectively inhibits bacterial β-lactamase activity.
- aBL presents a potential strategy to combat β-lactam resistance.
- Combination therapy with aBL and antibiotics may overcome antimicrobial resistance.
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