Fontana Carla R, Song Xiaoqing, Polymeri Angeliki, Goodson J Max, Wang Xiaoshan, Soukos Nikolaos S
Applied Molecular Photomedicine Laboratory, Department of Applied Oral Sciences, The Forsyth Institute, 245 First Street, Cambridge, MA, 02142, USA.
Department of Clinical Analysis, School of Pharmaceutical Sciences, University of São Paulo State (UNESP), 1621 Expedicionarios do Brasil Street, Araraquara, SP, 14801-960, Brazil.
Lasers Med Sci. 2015 Nov;30(8):2077-86. doi: 10.1007/s10103-015-1724-7. Epub 2015 Mar 11.
We have previously shown that blue light eliminates the black-pigmented oral bacteria Porphyromonas gingivalis, Prevotella intermedia, Prevotella nigrescens, and Prevotella melaninogenica. In the present study, the in vitro photosensitivity of the above black-pigmented microorganisms and four Fusobacteria species (Fusobacterium nucleatum ss. nucleatum, F. nucleatum ss. vincentii, F. nucleatum ss. polymorphum, Fusobacterium periodonticum) was investigated in pure cultures and human dental plaque suspensions. We also tested the hypothesis that phototargeting the above eight key periodontopathogens in plaque-derived biofilms in vitro would control growth within the dental biofilm environment. Cultures of the eight bacteria were exposed to blue light at 455 nm with power density of 80 mW/cm2 and energy fluence of 4.8 J/cm2. High-performance liquid chromatography (HPLC) analysis of bacteria was performed to demonstrate the presence and amounts of porphyrin molecules within microorganisms. Suspensions of human dental plaque bacteria were also exposed once to blue light at 455 nm with power density of 50 mW/cm2 and energy fluence of 12 J/cm2. Microbial biofilms developed from the same plaque were exposed to 455 nm blue light at 50 mW/cm2 once daily for 4 min (12 J/cm2) over a period of 3 days (4 exposures) in order to investigate the cumulative action of phototherapy on the eight photosensitive pathogens as well as on biofilm growth. Bacterial growth was evaluated using the colony-forming unit (CFU) assay. The selective phototargeting of pathogens was studied using whole genomic probes in the checkerboard DNA-DNA format. In cultures, all eight species showed significant growth reduction (p < 0.05). HPLC demonstrated various porphyrin patterns and amounts of porphyrins in bacteria. Following phototherapy, the mean survival fractions were reduced by 28.5 and 48.2% in plaque suspensions and biofilms, respectively, (p < 0.05). DNA probe analysis showed significant reduction in relative abundances of the eight bacteria as a group in plaque suspensions and biofilms. The cumulative blue light treatment suppressed biofilm growth in vitro. This may introduce a new avenue of prophylactic treatment for periodontal diseases.
我们之前已经表明,蓝光可清除产黑色素的口腔细菌牙龈卟啉单胞菌、中间普氏菌、变黑普氏菌和产黑色素普氏菌。在本研究中,我们对上述产黑色素微生物以及四种梭杆菌属细菌(具核梭杆菌具核亚种、具核梭杆菌文森亚种、具核梭杆菌多形亚种、牙周梭杆菌)在纯培养物和人类牙菌斑悬液中的体外光敏性进行了研究。我们还验证了这样一个假设,即体外对菌斑衍生生物膜中的上述八种关键牙周病原体进行光靶向作用可控制牙生物膜环境中的生长。将这八种细菌的培养物暴露于波长455 nm、功率密度80 mW/cm²、能量通量4.8 J/cm²的蓝光下。对细菌进行高效液相色谱(HPLC)分析,以证明微生物中卟啉分子的存在及含量。人类牙菌斑细菌悬液也暴露于波长455 nm、功率密度50 mW/cm²、能量通量12 J/cm²的蓝光下一次。从同一菌斑形成的微生物生物膜每天暴露于波长455 nm、功率密度50 mW/cm²的蓝光下一次,每次4分钟(12 J/cm²),持续3天(4次暴露),以研究光疗对这八种光敏病原体以及生物膜生长的累积作用。使用菌落形成单位(CFU)测定法评估细菌生长。使用棋盘式DNA - DNA格式的全基因组探针研究病原体的选择性光靶向作用。在培养物中,所有八个菌种均显示出显著的生长抑制(p < 0.05)。HPLC显示细菌中存在各种卟啉模式和卟啉含量。光疗后,菌斑悬液和生物膜中的平均存活分数分别降低了28.5%和48.2%(p < 0.05)。DNA探针分析显示,菌斑悬液和生物膜中这八种细菌作为一个群体的相对丰度显著降低。累积蓝光处理在体外抑制了生物膜生长。这可能为牙周疾病的预防性治疗引入一条新途径。