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Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms

Dental caries, an ecological dysbiosis of oral microflora, initiates from the virulent biofilms formed on tooth surfaces where cariogenic microorganisms metabolize dietary carbohydrates, producing acid that demineralizes tooth enamel. Forming cariogenic biofilms, Streptococcus mutans and Candida alb...

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Autores principales: Zeng, Yan, Fadaak, Ahmed, Alomeir, Nora, Wu, Tong Tong, Rustchenko, Elena, Qing, Shuang, Bao, Jianhang, Gilbert, Christie, Xiao, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980721/
https://www.ncbi.nlm.nih.gov/pubmed/35392605
http://dx.doi.org/10.3389/fcimb.2022.872012
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author Zeng, Yan
Fadaak, Ahmed
Alomeir, Nora
Wu, Tong Tong
Rustchenko, Elena
Qing, Shuang
Bao, Jianhang
Gilbert, Christie
Xiao, Jin
author_facet Zeng, Yan
Fadaak, Ahmed
Alomeir, Nora
Wu, Tong Tong
Rustchenko, Elena
Qing, Shuang
Bao, Jianhang
Gilbert, Christie
Xiao, Jin
author_sort Zeng, Yan
collection PubMed
description Dental caries, an ecological dysbiosis of oral microflora, initiates from the virulent biofilms formed on tooth surfaces where cariogenic microorganisms metabolize dietary carbohydrates, producing acid that demineralizes tooth enamel. Forming cariogenic biofilms, Streptococcus mutans and Candida albicans are well-recognized and emerging pathogens for dental caries. Recently, probiotics have demonstrated their potential in treating biofilm-related diseases, including caries. However, limited studies have assessed their effect on cariogenic bacteria–fungi cross-kingdom biofilm formation and their underlying interactions. Here, we assessed the effect of four probiotic Lactobacillus strains (Lactobacillus rhamnosus ATCC 2836, Lactobacillus plantarum ATCC 8014, Lactobacillus plantarum ATCC 14917, and Lactobacillus salivarius ATCC 11741) on S. mutans and C. albicans using a comprehensive multispecies biofilm model that mimicked high caries risk clinical conditions. Among the tested probiotic species, L. plantarum demonstrated superior inhibition on the growth of C. albicans and S. mutans, disruption of virulent biofilm formation with reduced bacteria and exopolysaccharide (EPS) components, and formation of virulent microcolonies structures. Transcriptome analysis (RNA sequencing) further revealed disruption of S. mutans and C. albicans cross-kingdom interactions with added L. plantarum. Genes of S. mutans and C. albicans involved in metabolic pathways (e.g., EPS formation, carbohydrate metabolism, glycan biosynthesis, and metabolism) were significantly downregulated. More significantly, genes related to C. albicans resistance to antifungal medication (ERG4), fungal cell wall chitin remodeling (CHT2), and resistance to oxidative stress (CAT1) were also significantly downregulated. In contrast, Lactobacillus genes plnD, plnG, and plnN that contribute to antimicrobial peptide plantaricin production were significantly upregulated. Our novel study findings support further assessment of the potential role of probiotic L. plantarum for cariogenic biofilm control.
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spelling pubmed-89807212022-04-06 Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms Zeng, Yan Fadaak, Ahmed Alomeir, Nora Wu, Tong Tong Rustchenko, Elena Qing, Shuang Bao, Jianhang Gilbert, Christie Xiao, Jin Front Cell Infect Microbiol Cellular and Infection Microbiology Dental caries, an ecological dysbiosis of oral microflora, initiates from the virulent biofilms formed on tooth surfaces where cariogenic microorganisms metabolize dietary carbohydrates, producing acid that demineralizes tooth enamel. Forming cariogenic biofilms, Streptococcus mutans and Candida albicans are well-recognized and emerging pathogens for dental caries. Recently, probiotics have demonstrated their potential in treating biofilm-related diseases, including caries. However, limited studies have assessed their effect on cariogenic bacteria–fungi cross-kingdom biofilm formation and their underlying interactions. Here, we assessed the effect of four probiotic Lactobacillus strains (Lactobacillus rhamnosus ATCC 2836, Lactobacillus plantarum ATCC 8014, Lactobacillus plantarum ATCC 14917, and Lactobacillus salivarius ATCC 11741) on S. mutans and C. albicans using a comprehensive multispecies biofilm model that mimicked high caries risk clinical conditions. Among the tested probiotic species, L. plantarum demonstrated superior inhibition on the growth of C. albicans and S. mutans, disruption of virulent biofilm formation with reduced bacteria and exopolysaccharide (EPS) components, and formation of virulent microcolonies structures. Transcriptome analysis (RNA sequencing) further revealed disruption of S. mutans and C. albicans cross-kingdom interactions with added L. plantarum. Genes of S. mutans and C. albicans involved in metabolic pathways (e.g., EPS formation, carbohydrate metabolism, glycan biosynthesis, and metabolism) were significantly downregulated. More significantly, genes related to C. albicans resistance to antifungal medication (ERG4), fungal cell wall chitin remodeling (CHT2), and resistance to oxidative stress (CAT1) were also significantly downregulated. In contrast, Lactobacillus genes plnD, plnG, and plnN that contribute to antimicrobial peptide plantaricin production were significantly upregulated. Our novel study findings support further assessment of the potential role of probiotic L. plantarum for cariogenic biofilm control. Frontiers Media S.A. 2022-03-22 /pmc/articles/PMC8980721/ /pubmed/35392605 http://dx.doi.org/10.3389/fcimb.2022.872012 Text en Copyright © 2022 Zeng, Fadaak, Alomeir, Wu, Rustchenko, Qing, Bao, Gilbert and Xiao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Zeng, Yan
Fadaak, Ahmed
Alomeir, Nora
Wu, Tong Tong
Rustchenko, Elena
Qing, Shuang
Bao, Jianhang
Gilbert, Christie
Xiao, Jin
Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title_full Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title_fullStr Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title_full_unstemmed Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title_short Lactobacillus plantarum Disrupts S. mutans–C. albicans Cross-Kingdom Biofilms
title_sort lactobacillus plantarum disrupts s. mutans–c. albicans cross-kingdom biofilms
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980721/
https://www.ncbi.nlm.nih.gov/pubmed/35392605
http://dx.doi.org/10.3389/fcimb.2022.872012
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