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      Antifungal and Antibiofilm Activities of B-Type Oligomeric Procyanidins From Commiphora leptophloeos Used Alone or in Combination With Fluconazole Against Candida spp.

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          Abstract

          Commiphora leptophloeos (Burseraceae) is a medicinal plant native to Brazil which is popularly used for treating oral and vaginal infections. There has been no scientific evidence pointing to its efficacy in the treatment of these infections. Thus, this study sought to investigate the cytotoxic, antifungal, and antibiofilm activity of C. leptophloeos against Candida spp. and to isolate, identify, and quantify the content of B-type oligomeric procyanidins (BDP) in the extract of C. leptophloeos stem bark. The extract and the n-butanol fraction were obtained by maceration and liquid-liquid partition, respectively. Phytochemical analysis performed by HPLC-PDA/ELSD and FIA-ESI-IT-MS/MS allowed the identification and quantification of BDP in the samples. The application of centrifugal partition chromatography helped isolate BDP, which was identified by 1H NMR and MS analyses. Candida spp. reference strains and clinical isolates (including fluconazole-resistant strains) derived from the blood cultures of candidemic patients and the vaginal secretion of patients with vulvovaginal candidiasis were used for evaluating the antifungal and antibiofilm effects. Minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC) were determined by the microdilution technique, and biofilm inhibition was evaluated through crystal violet and XTT assays. The combined action of BDP with fluconazole was determined by the checkerboard method. The extract, the n-butanol fraction, and the BDP exhibited antifungal activity with MIC values ranging from 312.5 to 2500 μg/mL and were found to significantly reduce the biofilm formed in all the Candida strains investigated. BDP showed a fungicidal potential against strains of Candida spp. (especially against fluconazole-resistant strains), with MIC and MFC values ranging from 156.2 to 2500 μg/mL. In addition, the combined application of BDP and fluconazole produced synergistic antifungal effects against resistant Candida spp. (FICI = 0.31–1.5). The cytotoxic properties of the samples evaluated in human erythrocytes through hemolytic test did not show hemolytic activity under active concentrations. The findings of the study show that C. leptophloeos has antifungal and antibiofilm potential but does not cause toxicity in human erythrocytes. Finally, BDP, which was isolated for the first time in C. leptophloeos, was found to exhibit antifungal effect against Candida spp. either when applied alone or in combination with fluconazole.

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          Quantification of biofilm in microtiter plates: overview of testing conditions and practical recommendations for assessment of biofilm production by staphylococci.

          The details of all steps involved in the quantification of biofilm formation in microtiter plates are described. The presented protocol incorporates information on assessment of biofilm production by staphylococci, gained both by direct experience as well as by analysis of methods for assaying biofilm production. The obtained results should simplify quantification of biofilm formation in microtiter plates, and make it more reliable and comparable among different laboratories.
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            Proanthocyanidins: A comprehensive review

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              Biofilm-Forming Capability of Highly Virulent, Multidrug-Resistant Candida auris

              The emerging multidrug-resistant yeast pathogen Candida auris has attracted considerable attention as a source of healthcare–associated infections. We report that this highly virulent yeast has the capacity to form antifungal resistant biofilms sensitive to the disinfectant chlorhexidine in vitro.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                22 February 2021
                2021
                : 12
                : 613155
                Affiliations
                [1] 1Laboratory of Pharmacognosy, Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Rio Grande do Norte , Natal, Brazil
                [2] 2Laboratory of Bioprospecting of Natural Products, São Paulo State University (UNESP) , São Paulo, Brazil
                [3] 3Laboratory of Phytochemistry, Institute of Chemistry, São Paulo State University (UNESP) , São Paulo, Brazil
                [4] 4Laboratory of Medical and Molecular Mycology, Department of Clinical and Toxicological Analyses, Federal University of Rio Grande do Norte , Natal, Brazil
                [5] 5Laboratory of Technology and Pharmaceutical Biotechnology (Tecbiofar), Faculty of Pharmacy, Federal University of Rio Grande do Norte , Natal, Brazil
                [6] 6Department of Health, University Center of Maurício de Nassau , Recife, Brazil
                [7] 7Laboratory of Pharmacognosy, Faculty of Pharmacy, University Paris Descartes , Paris, France
                Author notes

                Edited by: Miguel Cacho Teixeira, University of Lisbon, Portugal

                Reviewed by: Natália Cruz-Martins, Universidade do Porto, Portugal; Hamed Fakhim, Urmia University of Medical Sciences, Iran; Afsane Vaezi, Mazandaran University of Medical Sciences, Iran

                *Correspondence: Silvana Maria Zucolotto, silvanazucolotto@ 123456ufrnnet.br ; szucolotto@ 123456hotmail.com

                This article was submitted to Antimicrobials, Resistance and Chemotherapy, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2021.613155
                7937886
                790bd6f8-99cd-4c78-b4ed-6c7fa15e9b3c
                Copyright © 2021 Dantas-Medeiros, Zanatta, de Souza, Fernandes, Amorim-Carmo, Torres-Rêgo, Fernandes-Pedrosa, Vilegas, Araújo, Michel, Grougnet, Chaves and Zucolotto.

                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
                : 01 October 2020
                : 04 January 2021
                Page count
                Figures: 5, Tables: 5, Equations: 0, References: 67, Pages: 15, Words: 0
                Funding
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico 10.13039/501100003593
                Funded by: Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 10.13039/501100002322
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                burseraceae,fungal infections,biofilm,resistance,herbal drug,natural antifungal,imburana

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