2007
DOI: 10.1590/s0103-64402007000400011
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Detection of streptococcus mutans and streptococcus sobrinus in dental plaque samples from Brazilian preschool children by polymerase chain reaction

Abstract: The purposes of this study were to detect S. mutans and S. sobrinus by polymerase chain reaction (PCR) amplification, and to relate their presence to the incidence of dental caries in 42 Brazilian preschool children. Dental plaque samples were collected from the cervical margin of all erupted teeth of 5-6 years old children with primary dentition, using a sterile explorer. Examination of the dmft (decayed, missing, filled teeth) index, performed following the World Health Organization (WHO) caries diagnostic c… Show more

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Cited by 37 publications
(35 citation statements)
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“…The gtfB and gtfI genes of Streptococcus mutans and Streptococcus sobrinus respectively are suitable for designing PCR primers, as both genes express important virulence factors of the cariogenic bacteria and have nucleotide sequences specific to each species [17]. The same set of primers were used for the detection of S. mutans and S. sobrinus in studies done by Carmona et al [8], Seki et al [18] and Franco e Franco et al [19] and they yielded substantial results.…”
Section: Discussionmentioning
confidence: 99%
“…The gtfB and gtfI genes of Streptococcus mutans and Streptococcus sobrinus respectively are suitable for designing PCR primers, as both genes express important virulence factors of the cariogenic bacteria and have nucleotide sequences specific to each species [17]. The same set of primers were used for the detection of S. mutans and S. sobrinus in studies done by Carmona et al [8], Seki et al [18] and Franco e Franco et al [19] and they yielded substantial results.…”
Section: Discussionmentioning
confidence: 99%
“…The 16S ribosomal RNA gene was used to detect P. nigrescens ( 5 ' AT G A A A C A A A G G T T T T C C G G TA A G 3 ' 5'CCCACGTCTCTGTGGGGCTGCGA3' (804bp)) and P. intermedia (5'TTTGTTGGGGAGTAAAGCGGG3' and 5'TCAACATCTCTGTATCCTGCGT3' (575bp)) according to Tomazinho and Ávila-Campos (18). The target gene to detect S. mutans was the glucosyltransferase-I (5'ACTACACTTTCGGGTGGCTTGG3' and 5'CAGT ATAAGCGCCAGTTTCATC3'(517bp)) according to Franco and Franco et al (19) and the 16S ribosomal RNA gene was used to detect Actinomyces spp 5'CTTAGCTTGCTAAGTATGCCGTTTAG3' and 5'CAGCTGACTTATACTCCCGAAATC3' (889bp) according to Saba et al (7). Positive controls used in each experiment were the genomic DNA of S. mutans, P. nigrescens (ATCC 35406), P. intermedia (ATCC 25611) and Actinomyces spp (B19SC strain).…”
Section: Identification Of the Bacteria By Multiplex Pcrmentioning
confidence: 99%
“…The PCR reaction was performed in a volume of 25 µl under the following conditions: initial denaturation at 95 °C for 4 min, 30 cycles of denaturation at 95 °C for 30 s, annealing at 59 °C for 30 s and extension at 72 °C for 5 min. PCR-amplified products were then analysed by horizontal electrophoresis using a 1.5% agarose gel (Franco e Franco et al 2007). The primer sequences used in this study are provided in Table 1.…”
Section: Methodsmentioning
confidence: 99%