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Determination of Biofilm Initiation on Virus-infected Cells by Bacteria and Fungi
Published on: July 6, 2016
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Cellular Components Mediating Coadherence of Candida albicans and Fusobacterium nucleatum
Journal of Dental Research
|July 9, 2015
Summary
Researchers identified key molecules, FLO9 in Candida albicans and radD in Fusobacterium nucleatum, responsible for their coaggregation. This finding offers insights into treating oral polymicrobial infections by targeting these microbial interactions.
Area of Science:
- Microbiology
- Oral Biology
- Pathogenesis
Background:
- Candida albicans and Fusobacterium nucleatum are opportunistic pathogens often found together in oral diseases.
- Their physical coadherence facilitates colonization and contributes to polymicrobial pathogenesis.
- Previous research suggested carbohydrate and protein interactions mediate this coadherence, but specific components remained unknown.
Purpose of the Study:
- To identify the specific genetic determinants responsible for the coaggregation between Candida albicans and Fusobacterium nucleatum.
- To elucidate the molecular mechanisms underlying the physical interaction between these two oral pathogens.
Main Methods:
- Screening of a Candida albicans SN152 mutant library.
- Screening of a panel of Fusobacterium nucleatum 23726 outer membrane protein mutants.
- In vitro coaggregation assays using wild-type strains and identified mutants, with inhibition studies using arginine and mannose.
Main Results:
- Identification of FLO9 in C. albicans (encoding a mannoprotein) and radD in F. nucleatum (encoding an adhesin) as key genes mediating interspecies coadherence.
- Demonstration that arginine and mannose significantly inhibit the coaggregation between wild-type F. nucleatum and C. albicans.
- Evidence for a complex, multifaceted mechanism underlying the physical interaction between these species.
Conclusions:
- FLO9 and radD are major genetic components involved in Candida albicans-Fusobacterium nucleatum coaggregation.
- Targeting these identified adhesins and their associated molecules could lead to novel therapeutic strategies.
- Understanding these interactions provides crucial knowledge for developing treatments against polymicrobial oral diseases.
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