Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR
Background and Aims: Candida is an opportunistic pathogen that causes illness in people with a defective or weakened condition. Infectious diseases (periodontal diseases) are inflammatory and malignant inflammation of the dental-gum complex, in which the growth of biofilms caused by Candida glabrata...
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Format: | Article |
Language: | fas |
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Tehran University of Medical Sciences
2019-07-01
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Series: | Journal of Dental Medicine |
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Online Access: | http://jdm.tums.ac.ir/article-1-5865-en.html |
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author | Pooneh Mahmoudi Kiumarss Amini Parviz Amini |
author_facet | Pooneh Mahmoudi Kiumarss Amini Parviz Amini |
author_sort | Pooneh Mahmoudi |
collection | DOAJ |
description | Background and Aims: Candida is an opportunistic pathogen that causes illness in people with a defective or weakened condition. Infectious diseases (periodontal diseases) are inflammatory and malignant inflammation of the dental-gum complex, in which the growth of biofilms caused by Candida glabrata, Parapseilosis and Tropikalis is less than Candida albicans. Brown algae Sargasum is more compatible with human medicines due to having a natural origin than chemical drugs and has less side effects. The aim of the present study was to investigate the molecular characteristics of Candida species isolated from periodontal infections and the effect of Sargassum glaucescens extract on biofilm gene expression using Real-Time-PCR.
Materials and Methods: Oral samples of periodontal infection were collected from the referred patients. To isolate the candidate species, the specimens were cultured on a Sabouraud dextrose agar containing chloramphenicol (SDAc). The extracted DNA was extracted from colonies grown from Kit and Glass pearl. Grown chickens were identified by specific primers by PCR-RFLP method. In order to detect the expression of als genes in Candida isolates, RNA extraction was performed using Phenol-Chloroform and Pearl glass, and the CLSI-M27-A2 method was used to evaluate the effect of Sargasum glaucescens extract of algae.
Results: The results showed that the expression of als gene in periodontal infection is higher than other genes. Another role is als in the formation of Candida albicans biofilm. The minimum inhibitory concentration of fungal growth was 256 μg/ml by algae extract. Sargasum glaucescens reduced the expression of als gene expression by about 62% in the sample.
Conclusion: Sargasum glaucescens algae possesses specific pharmacological properties and antimicrobial and antimicrobial effects. The results of the study using Real Time PCR showed that expression of als gene in isolated studied with Sargasum algae extract was lower than untreated isolates. Thus, this indicated the positive role of treatment by sargasum glaucescens extract in reducing the expression of biofilm gene in isolates. |
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institution | Directory Open Access Journal |
issn | 1024-641X 2008-2444 |
language | fas |
last_indexed | 2024-12-22T10:47:37Z |
publishDate | 2019-07-01 |
publisher | Tehran University of Medical Sciences |
record_format | Article |
series | Journal of Dental Medicine |
spelling | doaj.art-dc62c4ec54614cbcb88460e16d71d5682022-12-21T18:28:53ZfasTehran University of Medical SciencesJournal of Dental Medicine1024-641X2008-24442019-07-013211121Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCRPooneh Mahmoudi0Kiumarss Amini1Parviz Amini2 Master of Microbiology, Department of Microbiology, Sirjan Branch, Faculty of Basic Sciences, Islamic Azad University, Sirjan, Iran Associate Professor, Department of Microbiology, Faculty of Basic Sciences, Saveh Branch, Islamic Azad University, Saveh, Iran Associate Professor, Department of Prosthodontics, School of Dentistry, Kerman University of Medical Sciences, Kerman, Iran Background and Aims: Candida is an opportunistic pathogen that causes illness in people with a defective or weakened condition. Infectious diseases (periodontal diseases) are inflammatory and malignant inflammation of the dental-gum complex, in which the growth of biofilms caused by Candida glabrata, Parapseilosis and Tropikalis is less than Candida albicans. Brown algae Sargasum is more compatible with human medicines due to having a natural origin than chemical drugs and has less side effects. The aim of the present study was to investigate the molecular characteristics of Candida species isolated from periodontal infections and the effect of Sargassum glaucescens extract on biofilm gene expression using Real-Time-PCR. Materials and Methods: Oral samples of periodontal infection were collected from the referred patients. To isolate the candidate species, the specimens were cultured on a Sabouraud dextrose agar containing chloramphenicol (SDAc). The extracted DNA was extracted from colonies grown from Kit and Glass pearl. Grown chickens were identified by specific primers by PCR-RFLP method. In order to detect the expression of als genes in Candida isolates, RNA extraction was performed using Phenol-Chloroform and Pearl glass, and the CLSI-M27-A2 method was used to evaluate the effect of Sargasum glaucescens extract of algae. Results: The results showed that the expression of als gene in periodontal infection is higher than other genes. Another role is als in the formation of Candida albicans biofilm. The minimum inhibitory concentration of fungal growth was 256 μg/ml by algae extract. Sargasum glaucescens reduced the expression of als gene expression by about 62% in the sample. Conclusion: Sargasum glaucescens algae possesses specific pharmacological properties and antimicrobial and antimicrobial effects. The results of the study using Real Time PCR showed that expression of als gene in isolated studied with Sargasum algae extract was lower than untreated isolates. Thus, this indicated the positive role of treatment by sargasum glaucescens extract in reducing the expression of biofilm gene in isolates.http://jdm.tums.ac.ir/article-1-5865-en.htmlCandida albicansBiofilmSargassum glaucescensReal time PCR |
spellingShingle | Pooneh Mahmoudi Kiumarss Amini Parviz Amini Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR Journal of Dental Medicine Candida albicans Biofilm Sargassum glaucescens Real time PCR |
title | Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR |
title_full | Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR |
title_fullStr | Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR |
title_full_unstemmed | Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR |
title_short | Molecular study of Candida albicans isolated from periodontal infections and effect of Sargasum alga extract on biofilm als gene expression using Real-Time-PCR |
title_sort | molecular study of candida albicans isolated from periodontal infections and effect of sargasum alga extract on biofilm als gene expression using real time pcr |
topic | Candida albicans Biofilm Sargassum glaucescens Real time PCR |
url | http://jdm.tums.ac.ir/article-1-5865-en.html |
work_keys_str_mv | AT poonehmahmoudi molecularstudyofcandidaalbicansisolatedfromperiodontalinfectionsandeffectofsargasumalgaextractonbiofilmalsgeneexpressionusingrealtimepcr AT kiumarssamini molecularstudyofcandidaalbicansisolatedfromperiodontalinfectionsandeffectofsargasumalgaextractonbiofilmalsgeneexpressionusingrealtimepcr AT parvizamini molecularstudyofcandidaalbicansisolatedfromperiodontalinfectionsandeffectofsargasumalgaextractonbiofilmalsgeneexpressionusingrealtimepcr |