Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque

Tooth decay is one of the most important problems societie. the activity of acid producing bacteria, especially Streptococcus mutans, is the main cause of this complication. The creation of the biofilms of the bacterium is subject to the presence of a specific enzyme called glucan sucrase or glucosy...

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Main Authors: fatemeh gharahkhani, amirhossein momen
Format: Article
Language:fas
Published: Neyshabur University of Medical Sciences 2019-09-01
Series:Majallah-i Dānishkadah-i ̒ulūm-i Pizishkī-i Niyshābūr
Subjects:
pcr
Online Access:http://journal.nums.ac.ir/article-1-710-en.html
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spelling doaj-11edd917d9d5457e966dfbe18867f31d2020-11-25T02:01:45ZfasNeyshabur University of Medical SciencesMajallah-i Dānishkadah-i ̒ulūm-i Pizishkī-i Niyshābūr2383-32032476-27682019-09-01736374Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaquefatemeh gharahkhani0amirhossein momen1 Department of Microbiology, School of Basic Sciences, Hamedan Branch, Islamic Azad University, Hamedan, Iran Department of Microbiology, School of Basic Sciences, Hamedan Branch, Islamic Azad University, Hamedan, Iran Tooth decay is one of the most important problems societie. the activity of acid producing bacteria, especially Streptococcus mutans, is the main cause of this complication. The creation of the biofilms of the bacterium is subject to the presence of a specific enzyme called glucan sucrase or glucosyltransferase, coded by gtf gene. The aim of this study was to evaluate the genes of GtfB and GtfC of Streptococcus mutans in the formation of dental plaque biofilm. Material & Mthod: . In study, the biofilm was formed on a polystyrene surface using a microtiter plate and stained. In order to confirm Streptococcus mutans colonies, biochemical and fermentative tests were performed. DNA extraction from the kit of gram-positive bacteria (Cinna Pure DNA KIT-PR881614) was used to extract DNA. To evaluate the PCR product, the samples were transferred to 1% agarose gel  examined staining. optimum pH and the effect of different concentrations of sucrose on bacterial growth were measured at 630 nm using spectropHotometer. Results: The results showed that out of 46 samples, 19 isolates (41.30%) had gtfB gene and 8 (17.4%) had gtfC gene. The absorbance of the biofilm produced by the samples is different and the highest absorption is 1.43. In this study, the highest growth rate of Streptococcus mutans isolated from tooth plaque was obtained at a concentration of 0.5 g / L sucrose and pH = 4.5. Conclusion: Therefore, sucrose sugar, which is commonly found in the diet, causes the growth of Streptococcus mutanshttp://journal.nums.ac.ir/article-1-710-en.htmlstreptococcus mutansgtfb genegtfc genebiofilmpcr
collection DOAJ
language fas
format Article
sources DOAJ
author fatemeh gharahkhani
amirhossein momen
spellingShingle fatemeh gharahkhani
amirhossein momen
Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
Majallah-i Dānishkadah-i ̒ulūm-i Pizishkī-i Niyshābūr
streptococcus mutans
gtfb gene
gtfc gene
biofilm
pcr
author_facet fatemeh gharahkhani
amirhossein momen
author_sort fatemeh gharahkhani
title Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
title_short Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
title_full Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
title_fullStr Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
title_full_unstemmed Evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
title_sort evaluation of phenotypic and molecular analysis of biofilm production in stereptococcus mutants producing dental plaque
publisher Neyshabur University of Medical Sciences
series Majallah-i Dānishkadah-i ̒ulūm-i Pizishkī-i Niyshābūr
issn 2383-3203
2476-2768
publishDate 2019-09-01
description Tooth decay is one of the most important problems societie. the activity of acid producing bacteria, especially Streptococcus mutans, is the main cause of this complication. The creation of the biofilms of the bacterium is subject to the presence of a specific enzyme called glucan sucrase or glucosyltransferase, coded by gtf gene. The aim of this study was to evaluate the genes of GtfB and GtfC of Streptococcus mutans in the formation of dental plaque biofilm. Material & Mthod: . In study, the biofilm was formed on a polystyrene surface using a microtiter plate and stained. In order to confirm Streptococcus mutans colonies, biochemical and fermentative tests were performed. DNA extraction from the kit of gram-positive bacteria (Cinna Pure DNA KIT-PR881614) was used to extract DNA. To evaluate the PCR product, the samples were transferred to 1% agarose gel  examined staining. optimum pH and the effect of different concentrations of sucrose on bacterial growth were measured at 630 nm using spectropHotometer. Results: The results showed that out of 46 samples, 19 isolates (41.30%) had gtfB gene and 8 (17.4%) had gtfC gene. The absorbance of the biofilm produced by the samples is different and the highest absorption is 1.43. In this study, the highest growth rate of Streptococcus mutans isolated from tooth plaque was obtained at a concentration of 0.5 g / L sucrose and pH = 4.5. Conclusion: Therefore, sucrose sugar, which is commonly found in the diet, causes the growth of Streptococcus mutans
topic streptococcus mutans
gtfb gene
gtfc gene
biofilm
pcr
url http://journal.nums.ac.ir/article-1-710-en.html
work_keys_str_mv AT fatemehgharahkhani evaluationofphenotypicandmolecularanalysisofbiofilmproductioninstereptococcusmutantsproducingdentalplaque
AT amirhosseinmomen evaluationofphenotypicandmolecularanalysisofbiofilmproductioninstereptococcusmutantsproducingdentalplaque
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