Real-time quantitative polymerase chain reaction for enumeration of Streptococcus mutans from oral samples

• Published in: European journal of oral sciences 2011-12, Vol.119 (6), p.447-454
• Main Authors: Childers, Noel K., Osgood, Robert C., Hsu, Kuei-Ling, Manmontri, Chanika, Momeni, Stephanie S., Mahtani, Harry K., Cutter, Gary R., Ruby, John D.
• Format: Article
• Language: English
• Subjects: Absorbance; Bacterial Typing Techniques - methods; Child; Child, Preschool; Children; Colony Count, Microbial; Colony-forming cells; copy number; Dental Caries - microbiology; Dental Caries - prevention & control; Dental Caries Susceptibility; dental plaque; Dentistry; Enumeration; Humans; Infant; Media (selective); Polymerase chain reaction; Primers; Real-Time Polymerase Chain Reaction; real-time quantitative polymerase chain reaction; saliva; Saliva - microbiology; Sensitivity and Specificity; Streptococcus mutans; Streptococcus mutans - isolation & purification; tongue
• ISSN: 0909-8836; 1600-0722
• DOI: 10.1111/j.1600-0722.2011.00888.x

Childers NK, Osgood RC, Hsu K‐L, Manmontri C, Momeni SS, Mahtani HK, Cutter GR, Ruby JD. Real‐time quantitative polymerase chain reaction for enumeration of Streptococcus mutans from oral samples. 
 Eur J Oral Sci 2011; 119: 447–454. © 2011 Eur J Oral Sci This study compared SYBR Green real‐time quantitative PCR (qPCR) with standard plate counting for the enumeration of Streptococcus mutans in oral samples. Oral samples (n = 710) were collected from high‐caries‐risk children for quantification of S. mutans by qPCR using primer pairs. The S. mutans copy number was calculated with reference to a qPCR quantification cycle (Cq) standard curve and compared with the absorbance value at 600 nm of a standard suspension of S. mutans UA159. The S. mutans copy number results were evaluated in relation to standard plate count (SPC) results obtained from each sample following culture on Petri plates containing S. mutans selective media and reported as colony‐forming units (CFUs). The mean S. mutans copy number calculated from qPCR was higher than the SPC CFUs (1.3 × 106 and 1.5 × 105 CFUs, respectively). The qPCR values were usually higher in individual samples and qPCR detected the presence of S. mutans 84% (231/276) of the time that the SPC did not, compared with 33% (4/12) of the time when qPCR failed to detect S. mutans and the SPC did. The qPCR technique was found to be more sensitive for detection of S. mutans from oral samples, a method that is not dependent on the viability of the sample taken and therefore is proposed as a more reliable and efficient means of quantification of S. mutans.