Please use this identifier to cite or link to this item: https://doi.org/10.1128/IAI.00339-19
Title: Multi-omics Analyses Reveal Synergistic Carbohydrate Metabolism in Streptococcus mutans-Candida albicans Mixed-Species Biofilms
Authors: Ellepola, K 
Truong, T 
Liu, Y
Lin, Q
Lim, TK
Lee, YM
Cao, T
Koo, H
Seneviratne, CJ 
Keywords: Science & Technology
Life Sciences & Biomedicine
Immunology
Infectious Diseases
Candida albicans
early-childhood caries
omics
Streptococcus mutans
mixed-species biofilms
EARLY-CHILDHOOD CARIES
DENTAL-CARIES
GENE
INHERITANCE
PROTEOMICS
TOLERANCE
CYTOSCAPE
CHILDREN
BACTERIA
Issue Date: 1-Oct-2019
Publisher: AMER SOC MICROBIOLOGY
Citation: Ellepola, K, Truong, T, Liu, Y, Lin, Q, Lim, TK, Lee, YM, Cao, T, Koo, H, Seneviratne, CJ (2019-10-01). Multi-omics Analyses Reveal Synergistic Carbohydrate Metabolism in Streptococcus mutans-Candida albicans Mixed-Species Biofilms. INFECTION AND IMMUNITY 87 (10). ScholarBank@NUS Repository. https://doi.org/10.1128/IAI.00339-19
Abstract: Candida albicans, a major opportunistic fungal pathogen, is frequently found together with Streptococcus mutans in dental biofilms associated with severe childhood caries (tooth decay), a prevalent pediatric oral disease. However, the impact of this cross-kingdom relationship on C. albicans remains largely uncharacterized. Here, we employed a novel quantitative proteomics approach in conjunction with transcriptomic profiling to unravel molecular pathways of C. albicans when cocultured with S. mutans in mixed biofilms. RNA sequencing and iTRAQ (isobaric tags for relative and absolute quantitation)-based quantitative proteomics revealed that C. albicans genes and proteins associated with carbohydrate metabolism were significantly enhanced, including sugar transport, aerobic respiration, pyruvate breakdown, and the glyoxylate cycle. Other C. albicans genes and proteins directly and indirectly related to cell morphogenesis and cell wall components such as mannan and glucan were also upregulated, indicating enhanced fungal activity in mixed-species biofilm. Further analyses revealed that S. mutans-derived exoenzyme gluco-syltransferase B (GtfB), which binds to the fungal cell surface to promote coadhesion, can break down sucrose into glucose and fructose that can be readily metabolized by C. albicans, enhancing growth and acid production. Altogether, we identified key pathways used by C. albicans in the mixed biofilm, indicating an active fungal role in the sugar metabolism and environmental acidification (key virulence traits associated with caries onset) when interacting with S. mutans, and a new cross-feeding mechanism mediated by GtfB that enhances C. albicans carbohydrate utilization. In addition, we demonstrate that comprehensive transcriptomics and quantitative proteomics can be powerful tools to study microbial contributions which remain underexplored in cross-kingdom biofilms.
Source Title: INFECTION AND IMMUNITY
URI: https://scholarbank.nus.edu.sg/handle/10635/205948
ISSN: 00199567
10985522
DOI: 10.1128/IAI.00339-19
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