Strategies to Potentiate Antimicrobial Photoinactivation by Overcoming Resistant Phenotypes

被引:105
作者
Adolfo Vera, Domingo Mariano [2 ]
Haynes, Mark H.
Ball, Anthony R. [3 ]
Dai, Tianhong [5 ]
Astrakas, Christos [6 ]
Kelso, Michael J. [7 ]
Hamblin, Michael R. [5 ,8 ]
Tegos, George P. [1 ,4 ,5 ]
机构
[1] Univ New Mexico, Sch Med, Dept Pathol, Ctr Mol Discovery, Albuquerque, NM 87131 USA
[2] Univ Nacl Mar del Plata, Fac Ciencias Exactas & Nat, Dept Chem, Mar Del Plata, Buenos Aires, Argentina
[3] Toxikon Corp, Bedford, MA USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Wellman Ctr Photomed, Boston, MA USA
[5] Harvard Univ, Sch Med, Dept Dermatol, Boston, MA 02115 USA
[6] Democritus Univ, Thrace Med Sch, Div Internal Med, Alexandroupolis, Greece
[7] Univ Wollongong, Sch Chem, Wollongong, NSW 2522, Australia
[8] Harvard MIT Div Hlth Sci & Technol, Cambridge, MA USA
关键词
MEDIATED PHOTODYNAMIC THERAPY; PSEUDOMONAS-AERUGINOSA BIOFILMS; GRAM-NEGATIVE BACTERIA; N-METHYL-PYRIDYL; STAPHYLOCOCCUS-AUREUS; MULTIDRUG TRANSPORTER; CRYSTAL-STRUCTURE; EFFLUX PUMP; IN-VITRO; ABC TRANSPORTERS;
D O I
10.1111/j.1751-1097.2012.01087.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Conventional antimicrobial strategies have become increasingly ineffective due to the emergence of multidrug resistance among pathogenic microorganisms. The need to overcome these deficiencies has triggered the exploration of alternative treatments and unconventional approaches towards controlling microbial infections. Photodynamic therapy (PDT) was originally established as an anticancer modality and is currently used in the treatment of age-related macular degeneration. The concept of photodynamic inactivation requires cell exposure to light energy, typically wavelengths in the visible region that causes the excitation of photosensitizer molecules either exogenous or endogenous, which results in the production of reactive oxygen species (ROS). ROS produce cell inactivation and death through modification of intracellular components. The versatile characteristics of PDT prompted its investigation as an anti-infective discovery platform. Advances in understanding of microbial physiology have shed light on a series of pathways, and phenotypes that serve as putative targets for antimicrobial drug discovery. Investigations of these phenotypic elements in concert with PDT have been reported focused on multidrug efflux systems, biofilms, virulence and pathogenesis determinants. In many instances the results are promising but only preliminary and require further investigation. This review discusses the different antimicrobial PDT strategies and highlights the need for highly informative and comprehensive discovery approaches.
引用
收藏
页码:499 / 511
页数:13
相关论文
共 129 条
[1]   Photochemical internalisation of chemotherapy potentiates killing of multidrug-resistant breast and bladder cancer cells [J].
Adigbli, D. K. ;
Wilson, D. G. G. ;
Farooqui, N. ;
Sousi, E. ;
Risley, P. ;
Taylor, I. ;
MacRobert, A. J. ;
Loizidou, M. .
BRITISH JOURNAL OF CANCER, 2007, 97 (04) :502-512
[2]  
AHMED M, 1993, J BIOL CHEM, V268, P11086
[3]   Crystal structure of the membrane fusion protein, MexA, of the multidrug transporter in Pseudomonas aeruginosa [J].
Akama, H ;
Matsuura, T ;
Kashiwagi, S ;
Yoneyama, H ;
Narita, SI ;
Tsukihara, T ;
Nakagawa, A ;
Nakae, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (25) :25939-25942
[4]   Molecular mechanisms of antibacterial multidrug resistance [J].
Alekshun, Michael N. ;
Levy, Stuart B. .
CELL, 2007, 128 (06) :1037-1050
[5]   Structure of P-Glycoprotein Reveals a Molecular Basis for Poly-Specific Drug Binding [J].
Aller, Stephen G. ;
Yu, Jodie ;
Ward, Andrew ;
Weng, Yue ;
Chittaboina, Srinivas ;
Zhuo, Rupeng ;
Harrell, Patina M. ;
Trinh, Yenphuong T. ;
Zhang, Qinghai ;
Urbatsch, Ina L. ;
Chang, Geoffrey .
SCIENCE, 2009, 323 (5922) :1718-1722
[6]   Promising Therapy of XDR-TB/MDR-TB with Thioridazine an Inhibitor of Bacterial Efflux Pumps [J].
Amaral, L. ;
Martins, M. ;
Viveiros, M. ;
Molnar, J. ;
Kristiansen, J. E. .
CURRENT DRUG TARGETS, 2008, 9 (09) :816-819
[7]   Structure-activity relationships of 2-aryl-1H-indole inhibitors of the NorA efflux pump in Staphylococcus aureus [J].
Ambrus, Joseph I. ;
Kelso, Michael J. ;
Bremner, John B. ;
Ball, Anthony R. ;
Casadei, Gabriele ;
Lewis, Kim .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (15) :4294-4297
[8]   RamA confers multidrug resistance in Salmonella enterica via increased expression of acrB, which is inhibited by chlorpromazine [J].
Bailey, Andrew M. ;
Paulsen, Ian T. ;
Piddock, Laura J. V. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (10) :3604-3611
[9]   Conjugating berberine to a multidrug resistance pump inhibitor creates an effective antimicrobial [J].
Ball, Anthony R. ;
Casadei, Gabriele ;
Samosorn, Siritron ;
Bremner, John B. ;
Ausubel, Frederick M. ;
Moy, Terence I. ;
Lewis, Kim .
ACS CHEMICAL BIOLOGY, 2006, 1 (09) :594-600
[10]   A WELL-BEHAVED ELECTROSTATIC POTENTIAL BASED METHOD USING CHARGE RESTRAINTS FOR DERIVING ATOMIC CHARGES - THE RESP MODEL [J].
BAYLY, CI ;
CIEPLAK, P ;
CORNELL, WD ;
KOLLMAN, PA .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (40) :10269-10280