Antimicrobial photodynamic therapy in a mouse model of Acinetobacter baumannii burn infection

Multi-drug resistant Acinetobacter baumanii infections represent a growing problem, especially in traumatic wounds and burns suffered by military personnel injured in Middle Eastern conflicts. Effective treatment using traditional antibiotics can be extremely difficult and new antimicrobial approaches are being investigated. One of these antimicrobial alternatives could be the combination of non-toxic photosensitizers (PS) and visible light known as photodynamic therapy (PDT). We report on the establishment of a new mouse model of full thickness thermal burns infected with a bioluminescent derivative of a clinical Iraqi isolate of A. baumannii and its PDT treatment by topical application of a PS produced by covalent conjugation chlorin(e6) to polyethylenimine followed by illumination of the burn surface with red light. Application of 108 A. baumannii cells to the surface of 10-second burns made on the dorsal surface of shaved female BALB/c mice led to chronic infections that lasted on average 22 days characterized by a remarkably stable bacterial bioluminescence. PDT carried out on day 0 soon after applying bacteria gave over three logs of loss of bacterial luminescence in a light exposure dependent manner, while PDT carried out on day 1 and day 2 gave approximately a 1.7-log reduction. Application of PS dissolved in 10% or 20% DMSO without light gave only modest reduction in bacterial luminescence from mouse burns. Some bacterial regrowth in the treated burn was observed but was generally modest. It was also found that PDT did not lead to inhibition of wound healing. The data suggest that PDT may be an effective new treatment for multi-drug resistant localized A. baumannii infections.

[1]  D. Gilpin Calculation of a new Meeh constant and experimental determination of burn size. , 1996, Burns : journal of the International Society for Burn Injuries.

[2]  R. Bonomo,et al.  Why are we afraid of Acinetobacter baumannii? , 2008, Expert review of anti-infective therapy.

[3]  J. Peto,et al.  Asymptotically Efficient Rank Invariant Test Procedures , 1972 .

[4]  J. Patel,et al.  An outbreak of multidrug-resistant Acinetobacter baumannii-calcoaceticus complex infection in the US military health care system associated with military operations in Iraq. , 2007, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[5]  Michael R Hamblin,et al.  Photodynamic Therapy Targeted to Pathogens , 2004, International journal of immunopathology and pharmacology.

[6]  J. Alexander,et al.  Relationship between extent of burn injury and magnitude of microbial translocation from the intestine. , 1993, The Journal of burn care & rehabilitation.

[7]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[8]  Z. Malik,et al.  Photodynamic inactivation of Gram-negative bacteria: problems and possible solutions. , 1992, Journal of photochemistry and photobiology. B, Biology.

[9]  J. Poulain,et al.  Comparative Analysis of Acinetobacters: Three Genomes for Three Lifestyles , 2008, PloS one.

[10]  C. Ryan,et al.  A quantitative model of invasive Pseudomonas infection in burn injury. , 1994, The Journal of burn care & rehabilitation.

[11]  J. Alexander,et al.  Comparison of translocation of different types of microorganisms from the intestinal tract of burned mice. , 2001, Shock.

[12]  Giulio Jori,et al.  Photodynamic therapy in the treatment of microbial infections: Basic principles and perspective applications , 2006, Lasers in surgery and medicine.

[13]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .

[14]  W. Manson,et al.  Intestinal bacterial translocation in experimentally burned mice with wounds colonized by Pseudomonas aeruginosa. , 1992, The Journal of trauma.

[15]  Tayyaba Hasan,et al.  Rapid Control of Wound Infections by Targeted Photodynamic Therapy Monitored by In Vivo Bioluminescence Imaging¶ , 2002 .

[16]  Faten Gad,et al.  Protease-Stable Polycationic Photosensitizer Conjugates between Polyethyleneimine and Chlorin(e6) for Broad-Spectrum Antimicrobial Photoinactivation , 2006, Antimicrobial Agents and Chemotherapy.

[17]  Shouguang Jin,et al.  Expression of the soxR Gene ofPseudomonas aeruginosa Is Inducible during Infection of Burn Wounds in Mice and Is Required To Cause Efficient Bacteremia , 1999, Infection and Immunity.

[18]  A. Habeeb,et al.  Determination of free amino groups in proteins by trinitrobenzenesulfonic acid. , 1966, Analytical biochemistry.

[19]  E. Hultén,et al.  Acinetobacter baumannii infections among patients at military medical facilities treating injured U.S. service members, 2002-2004. , 2004, MMWR. Morbidity and mortality weekly report.

[20]  S. Tu,et al.  Cloning and nucleotide sequences of lux genes and characterization of luciferase of Xenorhabdus luminescens from a human wound , 1991, Journal of Bacteriology.

[21]  Michael R Hamblin,et al.  Photodynamic therapy: a new antimicrobial approach to infectious disease? , 2004, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[22]  A. Peleg Optimizing therapy for Acinetobacter baumannii. , 2007, Seminars in respiratory and critical care medicine.

[23]  Á. Villanueva,et al.  Meso-substituted cationic porphyrins as efficient photosensitizers of gram-positive and gram-negative bacteria. , 1996, Journal of photochemistry and photobiology. B, Biology.