4.6 Article

Potentiated antimicrobial blue light killing of methicillin resistant Staphylococcus aureus by pyocyanin

Journal

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotobiol.2020.112109

Keywords

MRSA; Pyocyanin; Antimicrobial blue light; Wound infection; Antimicrobial resistance

Funding

  1. National Institute Health [R01AI123312]
  2. U.S. Department of Defense [FA9550-171-0277]
  3. American Society for Laser Medicine and Surgery Research [BS.F04.18, BS.01.20]

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The study investigated the antimicrobial capabilities of the innovative combination of antimicrobial blue light (aBL) with Pseudomonas aeruginosa pigment pyocyanin against methicillin resistant Staphylococcus aureus (MSRA). The results showed that pyocyanin potentiated aBL activity and could bleach staphyloxanthin within MRSA colonies, significantly reducing MRSA viability in a proof-of-principle early onset MRSA skin abrasion infection model. The combination of aBL and pyocyanin represents a potentially powerful therapeutic modality for the treatment of MRSA infections.
As antimicrobial resistance continues to threaten the efficacy of conventional antibiotic therapy, it is paramount that we investigate innovative approaches to treat infectious diseases. In this study, we investigated the antimicrobial capabilities of the innovative combination of antimicrobial blue light (aBL; 405 nm wavelength) with the Pseudomonas aeruginosa pigment pyocyanin against methicillin resistant Staphylococcus aureus (MSRA. We explored the effects of different radiant exposures of aBL and increasing concentrations of pyocyanin against planktonic cells and those within biofilms. In addition, we investigated the effect of the aBL/pyocyanin on the endogenous staphyloxanthin pigment, as well as the role of hydrogen peroxide and singlet oxygen scavenging in the efficacy of this combination. Lastly, we investigated the potential for the aBL/pyocyanin to reduce the MRSA burden within a proof-of-principle mouse abrasion infection model. We found pyocyanin to be a powerful potentiator of aBL activity under all in vitro conditions tested. In addition, we serendipitously discovered the capability of the aBL/pyocyanin combination to bleach staphyloxanthin within colonies of MRSA. Furthermore, we established that singlet oxygen is an important mediator during combined aBL/pyocyanin exposure. Moreover, we found that the combination of aBL and pyocyanin could significantly reduce the viability of MRSA within a proof-of-principle early onset MRSA skin abrasion infection. Exposure to the treatment did not have deleterious effects on skin tissue. In conclusion, the combination of aBL and pyocyanin represents a potentially powerful therapeutic modality for the treatment of infections caused by MRSA.

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