TY - JOUR
T1 - Antimicrobial Blue Light Inactivation of Gram-Negative Pathogens in Biofilms
T2 - In Vitro and in Vivo Studies
AU - Wang, Yucheng
AU - Wu, Ximing
AU - Chen, Jia
AU - Amin, Rehab
AU - Lu, Min
AU - Bhayana, Brijesh
AU - Zhao, Jie
AU - Murray, Clinton K.
AU - Hamblin, Michael R.
AU - Hooper, David C.
AU - Dai, Tianhong
N1 - Publisher Copyright:
© 2015 The Author 2016.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Background. Biofilms affect >80% bacterial infections in human and are usually difficult to eradicate because of their inherent drug resistance. Methods. We investigated the effectiveness of antimicrobial blue light (aBL) (wavelength, 415 nm) for inactivating Acinetobacter baumannii or Pseudomonas aeruginosa biofilms in 96-well microplates or infected mouse burn wounds. Results. In vitro, in 96-well microplates, exposure of 24-hour-old and 72-hour-old A. baumannii biofilms to 432 J/cm2 aBL resulted in inactivation of 3.59 log10 and 3.18 log10 colony-forming units (CFU), respectively. For P. aeruginosa biofilms, similar levels of inactivation - 3.02 log10 and 3.12 log10 CFU, respectively - were achieved. In mouse burn wounds infected with 5 × 106 CFU of A. baumannii, approximately 360 J/cm2 and 540 J/cm2 aBL was required to inactivate 3 log10 CFU in biofilms when delivered 24 and 48 hours, respectively, after bacterial inoculation. High-performance liquid chromatography analysis revealed the presence of endogenous porphyrins in both A. baumannii and P. aeruginosa. TUNEL assay detected no apoptotic cells in aBL-irradiated mouse skin at up to 24 hours after aBL exposure (540 J/cm2). Conclusions. aBL has antimicrobial activity in biofilms of A. baumannii and P. aeruginosa and is a potential therapeutic approach for biofilm-related infections.
AB - Background. Biofilms affect >80% bacterial infections in human and are usually difficult to eradicate because of their inherent drug resistance. Methods. We investigated the effectiveness of antimicrobial blue light (aBL) (wavelength, 415 nm) for inactivating Acinetobacter baumannii or Pseudomonas aeruginosa biofilms in 96-well microplates or infected mouse burn wounds. Results. In vitro, in 96-well microplates, exposure of 24-hour-old and 72-hour-old A. baumannii biofilms to 432 J/cm2 aBL resulted in inactivation of 3.59 log10 and 3.18 log10 colony-forming units (CFU), respectively. For P. aeruginosa biofilms, similar levels of inactivation - 3.02 log10 and 3.12 log10 CFU, respectively - were achieved. In mouse burn wounds infected with 5 × 106 CFU of A. baumannii, approximately 360 J/cm2 and 540 J/cm2 aBL was required to inactivate 3 log10 CFU in biofilms when delivered 24 and 48 hours, respectively, after bacterial inoculation. High-performance liquid chromatography analysis revealed the presence of endogenous porphyrins in both A. baumannii and P. aeruginosa. TUNEL assay detected no apoptotic cells in aBL-irradiated mouse skin at up to 24 hours after aBL exposure (540 J/cm2). Conclusions. aBL has antimicrobial activity in biofilms of A. baumannii and P. aeruginosa and is a potential therapeutic approach for biofilm-related infections.
KW - Acinetobacter baumannii
KW - HPLCantimicrobial blue light
KW - Pseudomonas aeruginosa
KW - TUNEL assay
KW - biofilm
KW - bioluminescence imaging HPLC
KW - burn wound
KW - endogenous porphyrins
KW - mouse model
UR - http://www.scopus.com/inward/record.url?scp=84971643889&partnerID=8YFLogxK
U2 - 10.1093/infdis/jiw070
DO - 10.1093/infdis/jiw070
M3 - Article
C2 - 26908743
AN - SCOPUS:84971643889
SN - 0022-1899
VL - 213
SP - 1380
EP - 1387
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 9
ER -