Photodynamic inactivation of clinical isolates of Candida using Photodithazine®

被引:54
作者
Dovigo, L. N. [1 ]
Carmello, J. C. [2 ]
Carvalho, M. T. [3 ]
Mima, E. G. [2 ]
Vergani, C. E. [2 ]
Bagnato, V. S. [3 ]
Pavarina, A. C. [2 ]
机构
[1] UNESP Univ Estadual Paulista, Araraquara Dent Sch, Dept Social Dent, Araraquara, Brazil
[2] UNESP Univ Estadual Paulista, Araraquara Dent Sch, Dept Dent Mat & Prosthodont, Araraquara, Brazil
[3] Univ Sao Paulo, Phys Inst Sao Carlos, Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
photodynamic therapy; Candida spp; biofilms; BIOFILM FORMATION; YEAST-CELLS; DENTURE STOMATITIS; ORAL CANDIDIASIS; TOLUIDINE-BLUE; ALBICANS; THERAPY; SUSCEPTIBILITY; MICROORGANISMS; DERIVATIVES;
D O I
10.1080/08927014.2013.827668
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study evaluated the photodynamic inactivation (PDI) mediated by Photodithazine((R)) (PDZ) against 15 clinical isolates of Candida albicans, Candida glabrata and Candida tropicalis. Each isolate, in planktonic and biofilm form, was exposed to PDI by assessing a range of PDZ concentrations and light emitting diode fluences. Cell survival of the planktonic suspensions was determined by colony forming units (CFU ml(-1)). The antifungal effects of PDI against biofilms were evaluated by CFUml(-1) and metabolic assay. Data were analyzed by non-parametric tests (=0.05). Regardless of the species, PDI promoted a significant viability reduction of planktonic yeasts. The highest reduction in cell viability of the biofilms was equivalent to 0.9 log(10) (CFU ml(-1)) for C. albicans, while 1.4 and 1.5 log(10) reductions were obtained for C. tropicalis and C. glabrata, respectively. PDI reduced the metabolic activity of biofilms by 62.1, 76.0, and 76.9% for C. albicans, C. tropicalis, and C. glabrata, respectively. PDZ-mediated PDI promoted significant reduction in the viability of Candida isolates.
引用
收藏
页码:1057 / 1067
页数:11
相关论文
共 64 条
[1]   ANIMAL-MODELS OF ORAL CANDIDIASIS - A REVIEW [J].
ALLEN, CM .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1994, 78 (02) :216-221
[2]  
BERTOLONI G, 1992, MICROBIOS, V71, P33
[3]  
BERTOLONI G, 1989, J GEN MICROBIOL, V135, P957
[4]   Susceptibility of Candida species to photodynamic effects of photofrin [J].
Bliss, JM ;
Bigelow, CE ;
Foster, TH ;
Haidaris, CG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) :2000-2006
[5]   Photobleaching of sensitisers used in photodynamic therapy [J].
Bonnett, R ;
Martínez, G .
TETRAHEDRON, 2001, 57 (47) :9513-9547
[6]   Intracellular reactive oxygen species in monocytes generated by photosensitive chromophores activated with blue light [J].
Bouillaguet, Serge ;
Owen, Brandi ;
Wataha, John C. ;
Campo, Marino A. ;
Lange, Norbert ;
Schrenzel, Jacques .
DENTAL MATERIALS, 2008, 24 (08) :1070-1076
[7]   Photodynamic Antifungal Chemotherapy [J].
Calzavara-Pinton, Piergiacomo ;
Rossi, M. Teresa ;
Sala, Raffaella ;
Venturini, Marina .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2012, 88 (03) :512-522
[8]   Fungicidal properties of meso-arylglycosylporphyrins:: influence of sugar substituents on photoinduced damage in the yeast Saccharomyces cerevisiae [J].
Carré, V ;
Gaud, O ;
Sylvain, I ;
Bourdon, O ;
Spiro, M ;
Blais, J ;
Granet, R ;
Krausz, P ;
Guilloton, M .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1999, 48 (01) :57-62
[9]   Biofilm formation by the fungal pathogen Candida albicans:: Development, architecture, and drug resistance [J].
Chandra, J ;
Kuhn, DM ;
Mukherjee, PK ;
Hoyer, LL ;
McCormick, T ;
Ghannoum, MA .
JOURNAL OF BACTERIOLOGY, 2001, 183 (18) :5385-5394
[10]   Photolon™, a chlorin e6 derivative, triggers ROS production and light-dependent cell death via necrosis [J].
Copley, Louise ;
van der Watt, Pauline ;
Wirtz, Karel W. ;
Parker, M. Iqbal ;
Leaner, Vima D. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2008, 40 (02) :227-235