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      Lichen Polyphenolic Compounds for the Eradication of Candida albicans Biofilms

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          Abstract

          Lichens, due to their symbiotic nature (association between fungi and algae), constitute a chemical factory of original compounds. Polyphenolic compounds (depsides and depsidones) are the main constituents of lichens and are exclusively biosynthesized by these organisms. A panel of 11 polyphenols was evaluated for their anti-biofilm activity against Candida albicans biofilms on the maturation phase (anti-maturation) (MMIC 50) as well as on preformed 24-h-old biofilm (anti-biofilm) (MBIC 50) using the XTT assay. Minimum inhibitory concentrations of compounds (MICs) against C. albicans planktonic yeast were also determined using a broth microdilution method. While none of the tested compounds were active against planktonic cells (IC 50 > 100 µg/ml), three depsides slowed the biofilm maturation (MMIC 50 ≤12.5 µg/ml after 48 h of contact with Candida cells). Evernic acid was able to both slow the maturation and reduce the already formed biofilms with MBIC 50 ≤12.5 µg/ml after 48 h of contact with the biofilm. This compound shows a weak toxicity against HeLa cells (22%) at the minimal active concentration and no hemolytic activity at 100 µg/ml. Microscopic observations of evernic acid and optimization of its solubility were performed to further study this compound. This work confirmed the anti-biofilm potential of depsides, especially evernic acid, and allows to establish the structure–activity relationships to better explain the anti-biofilm potential of these compounds.

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          Biofilms: Survival Mechanisms of Clinically Relevant Microorganisms

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            Biofilm formation by the fungal pathogen Candida albicans: development, architecture, and drug resistance.

            Biofilms are a protected niche for microorganisms, where they are safe from antibiotic treatment and can create a source of persistent infection. Using two clinically relevant Candida albicans biofilm models formed on bioprosthetic materials, we demonstrated that biofilm formation proceeds through three distinct developmental phases. These growth phases transform adherent blastospores to well-defined cellular communities encased in a polysaccharide matrix. Fluorescence and confocal scanning laser microscopy revealed that C. albicans biofilms have a highly heterogeneous architecture composed of cellular and noncellular elements. In both models, antifungal resistance of biofilm-grown cells increased in conjunction with biofilm formation. The expression of agglutinin-like (ALS) genes, which encode a family of proteins implicated in adhesion to host surfaces, was differentially regulated between planktonic and biofilm-grown cells. The ability of C. albicans to form biofilms contrasts sharply with that of Saccharomyces cerevisiae, which adhered to bioprosthetic surfaces but failed to form a mature biofilm. The studies described here form the basis for investigations into the molecular mechanisms of Candida biofilm biology and antifungal resistance and provide the means to design novel therapies for biofilm-based infections.
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              The mycobiota: interactions between commensal fungi and the host immune system.

              The body is host to a wide variety of microbial communities from which the immune system protects us and that are important for the normal development of the immune system and for the maintenance of healthy tissues and physiological processes. Investigators have mostly focused on the bacterial members of these communities, but fungi are increasingly being recognized to have a role in defining these communities and to interact with immune cells. In this Review, we discuss what is currently known about the makeup of fungal communities in the body and the features of the immune system that are particularly important for interacting with fungi at these sites.
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                Author and article information

                Contributors
                Journal
                Front Cell Infect Microbiol
                Front Cell Infect Microbiol
                Front. Cell. Infect. Microbiol.
                Frontiers in Cellular and Infection Microbiology
                Frontiers Media S.A.
                2235-2988
                16 September 2021
                2021
                : 11
                : 698883
                Affiliations
                [1] 1UMR CNRS 7267, Laboratoire Ecologie et Biologie des Interactions, Université de Poitiers , Poitiers, France
                [2] 2EA 7500, Laboratoire PEIRENE, Université de Limoges , Limoges, France
                Author notes

                Edited by: Claus Moser, Rigshospitalet, Denmark

                Reviewed by: Ai-Qun Jia, Hainan University, China; Karishma S. Kaushik, Savitribai Phule Pune University, India

                *Correspondence: Marion Millot, marion.millot@ 123456unilim.fr

                †These authors have contributed equally to this work and share first authorship

                This article was submitted to Biofilms, a section of the journal Frontiers in Cellular and Infection Microbiology

                Article
                10.3389/fcimb.2021.698883
                8481799
                34604104
                8ad604d2-b923-476b-8937-d2b4a4cf794d
                Copyright © 2021 Girardot, Millot, Hamion, Billard, Juin, Ntoutoume, Sol, Mambu and Imbert

                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.

                History
                : 22 April 2021
                : 19 August 2021
                Page count
                Figures: 3, Tables: 2, Equations: 0, References: 46, Pages: 10, Words: 5847
                Categories
                Cellular and Infection Microbiology
                Original Research

                Infectious disease & Microbiology
                depsides,lichens,biofilm,candida albicans,evernic acid
                Infectious disease & Microbiology
                depsides, lichens, biofilm, candida albicans, evernic acid

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