Real-time imaging and quantification of bioluminescent bacteria in root canals in vitro

被引:34
作者
Sedgley, C
Applegate, B
Nagel, A
Hall, D
机构
[1] Univ Michigan, Sch Dent, Dept Cariol Restorat Sci & Endodont, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Dent, Dept Radiol, Ann Arbor, MI 48109 USA
[3] Purdue Univ, Dept Food Sci, W Lafayette, IN 47907 USA
关键词
D O I
10.1097/01.DON.0000132299.02265.6C
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The detection of microorganisms in root canals is generally limited to qualitative or semiquantitative methods. We describe a new and nondestructive in vitro method to quantify root-canal bacteria over sequential treatment procedures using real-time imaging in conjunction with the bioluminescent reporter strain Pseudomonas fluorescens 5RL. Induced bacterial photon emission can be monitored by sensitive optical photonic imaging and luminometry, providing images as well as spatial and quantitative measurements. Bioluminescence imaging and luminometry determined that the lower limit of detection of bacteria in root canals occurred between 2 x 102 and 2 x 103 cells, with high correlation between cell counts and detection devices (r greater than or equal to 0.981). A preliminary study assessed the efficacy of sequential irrigation procedures to remove 5 x 106 bacteria from root canals (n = 5; apical size 60) using a 28-gauge, endodontic needle positioned 1 mm from working length; 9.2% +/- 3.1% and 8% +/- 3.6% of bacteria remained after 3 and 6 ml irrigation, respectively (p = 0.03), corresponding to approximately 4 x 10(5) bacteria remaining after 6 ml. This method can be used to study the efficacy of sequential endodontic treatment procedures in removing bacteria from root canals.
引用
收藏
页码:893 / 898
页数:6
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