4.7 Article

Antimicrobial Blue Light Therapy for Multidrug-Resistant Acinetobacter baumannii Infection in a Mouse Burn Model: Implications for Prophylaxis and Treatment of Combat-related Wound Infections

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 209, 期 12, 页码 1963-1971

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jit842

关键词

Blue light; Acinetobacter baumannii; burn; infection; multidrug resistance; mouse model

资金

  1. Center for Integration of Medicine and Innovative Technology (CIMIT) under a US Army Medical Research Acquisition Activity [13-1033]
  2. COTA/Smith and Nephew [2012-16]
  3. Airlift Research Foundation [109421]
  4. National Institutes of Health [RO1AI050875]

向作者/读者索取更多资源

In this study, we investigated the utility of antimicrobial blue light therapy for multidrug-resistant Acinetobacter baumannii infection in a mouse burn model. A bioluminescent clinical isolate of multidrug-resistant A. baumannii was obtained. The susceptibility of A. baumannii to blue light (415 nm)-inactivation was compared in vitro to that of human keratinocytes. Repeated cycles of sublethal inactivation of bacterial by blue light were performed to investigate the potential resistance development of A. baumannii to blue light. A mouse model of third degree burn infected with A. baumannii was developed. A single exposure of blue light was initiated 30 minutes after bacterial inoculation to inactivate A. baumannii in mouse burns. It was found that the multidrug-resistant A. baumannii strain was significantly more susceptible than keratinocytes to blue light inactivation. Transmission electron microscopy revealed blue light-induced ultrastructural damage in A. baumannii cells. Fluorescence spectroscopy suggested that endogenous porphyrins exist in A. baumannii cells. Blue light at an exposure of 55.8 J/cm(2) significantly reduced the bacterial burden in mouse burns. No resistance development to blue light inactivation was observed in A. baumannii after 10 cycles of sublethal inactivation of bacteria. No significant DNA damage was detected in mouse skin by means of a skin TUNEL assay after a blue light exposure of 195 J/cm(2).

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