OBJECTIVE: To explore the fluorescence characteristics of common cariogenic bacteria: Streptococcus mutans, S. sanguis, Actinomyces viscosus, Prevotella intermedia, Lactobacillus acidophilus, and Candida albicans. METHODS: The bacteria were cultured on brain heart infusion (BHI) agar and BHI blood agar, and bacterial colonies were collected for further amplification in liquid medium. Bacterial suspensions in physiological saline were equally divided into three parts for bacteria counting, fluorescence spectrometry detection, and fluorescence microscope examination. RESULTS: The optimal excitation wavelength of the bacteria was 350 nm; their characteristic fluorescence peak position was at 436 ± 4 nm. There was a significant linear correlation between fluorescence intensity and bacterial concentration. The mean optical density (MOD) of S. mutans and L. acidophilus cultivated in BHI blood was significantly higher than that cultivated in BHI agar (110 ± 10 vs. 57 ± 20; 94 ± 16 vs. 31 ± 12, respectively, P < 0.05). The MOD of S. sanguis, A. viscosus, and P. intermedia cultivated in BHI blood agar was higher than that cultivated in BHI agar (37 ± 12 vs. 36 ± 11; 43 ± 17 vs. 38 ± 6; 86 ± 21 vs. 72 ± 8, respectively, P > 0.05); the opposite was observed for C. albicans. CONCLUSION: At 350 nm excitation wavelength, 436 ± 4 nm is an indicator for detecting six cariogenic bacteria. The fluorescence energy, Q, is a valuable index reflecting bacterial concentration under fluorescence spectrometry detection. Exogenous fluorescence groups have greater influence on fluorescence intensity and little influence on fluorescence peak position detection.
OBJECTIVE: To explore the fluorescence characteristics of common cariogenic bacteria: Streptococcus mutans, S. sanguis, Actinomyces viscosus, Prevotella intermedia, Lactobacillus acidophilus, and Candida albicans. METHODS: The bacteria were cultured on brain heart infusion (BHI) agar and BHI blood agar, and bacterial colonies were collected for further amplification in liquid medium. Bacterial suspensions in physiological saline were equally divided into three parts for bacteria counting, fluorescence spectrometry detection, and fluorescence microscope examination. RESULTS: The optimal excitation wavelength of the bacteria was 350 nm; their characteristic fluorescence peak position was at 436 ± 4 nm. There was a significant linear correlation between fluorescence intensity and bacterial concentration. The mean optical density (MOD) of S. mutans and L. acidophilus cultivated in BHI blood was significantly higher than that cultivated in BHI agar (110 ± 10 vs. 57 ± 20; 94 ± 16 vs. 31 ± 12, respectively, P < 0.05). The MOD of S. sanguis, A. viscosus, and P. intermedia cultivated in BHI blood agar was higher than that cultivated in BHI agar (37 ± 12 vs. 36 ± 11; 43 ± 17 vs. 38 ± 6; 86 ± 21 vs. 72 ± 8, respectively, P > 0.05); the opposite was observed for C. albicans. CONCLUSION: At 350 nm excitation wavelength, 436 ± 4 nm is an indicator for detecting six cariogenic bacteria. The fluorescence energy, Q, is a valuable index reflecting bacterial concentration under fluorescence spectrometry detection. Exogenous fluorescence groups have greater influence on fluorescence intensity and little influence on fluorescence peak position detection.
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