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      Fluconazole impacts the extracellular matrix of fluconazole-susceptible and -resistant Candida albicans and Candida glabrata biofilms

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          ABSTRACT

          Background: Fluconazole (FLZ) is a drug commonly used for the treatment of Candida infections. However, β-glucans in the extracellular matrices (ECMs) hinder FLZ penetration into Candida biofilms, while extracellular DNA (eDNA) contributes to the biofilm architecture and resistance.

          Methods: This study characterized biofilms of FLZ-sensitive (S) and -resistant (R) Candida albicans and Candida glabrata in the presence or absence of FLZ focusing on the ECM traits. Biofilms of C. albicans American Type Culture Collection (ATCC) 90028 (CaS), C. albicans ATCC 96901 (CaR), C. glabrata ATCC 2001 (CgS), and C. glabrata ATCC 200918 (CgR) were grown in RPMI medium with or without FLZ at 5× the minimum inhibitory concentration (37°C/48 h). Biofilms were assessed by colony-forming unit (CFU)/mL, biomass, and ECM components (alkali-soluble polysaccharides [ASP], water-soluble polysaccharides [WSP], eDNA, and proteins). Scanning electron microscopy (SEM) was also performed. Data were analyzed by parametric and nonparametric tests ( α  =  0.05).

          Results: In biofilms, FLZ reduced the CFU/mL of all strains ( p < 0.001), except for CaS ( p = 0.937). However, the ASP quantity in CaS was significantly reduced by FLZ ( p = 0.034), while the drug had no effect on the ASP levels in other strains ( p > 0.05). Total biomasses and WSP were significantly reduced by FLZ in the ECM of all yeasts ( p < 0.001), but levels of eDNA and proteins were unaffected ( p > 0.05). FLZ affected the cell morphology and biofilm structure by hindering hyphae formation in CaS and CaR biofilms, by decreasing the number of cells in CgS and CgR biofilms, and by yielding sparsely spaced cell agglomerates on the substrate.

          Conclusion: FLZ impacts biofilms of C. albicans and C. glabrata as evident by reduced biomass. This reduced biomass coincided with lowered cell numbers and quantity of WSPs. Hyphal production by C. albicans was also reduced.

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          Mechanisms of biofilm resistance to antimicrobial agents.

          Biofilms are communities of microorganisms attached to a surface. It has become clear that biofilm-grown cells express properties distinct from planktonic cells, one of which is an increased resistance to antimicrobial agents. Recent work has indicated that slow growth and/or induction of an rpoS-mediated stress response could contribute to biocide resistance. The physical and/or chemical structure of exopolysaccharides or other aspects of biofilm architecture could also confer resistance by exclusion of biocides from the bacterial community. Finally, biofilm-grown bacteria might develop a biofilm-specific biocide-resistant phenotype. Owing to the heterogeneous nature of the biofilm, it is likely that there are multiple resistance mechanisms at work within a single community. Recent research has begun to shed light on how and why surface-attached microbial communities develop resistance to antimicrobial agents.
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            The cidA murein hydrolase regulator contributes to DNA release and biofilm development in Staphylococcus aureus.

            The Staphylococcus aureus cidA and lrgA genes have been shown to affect cell lysis under a variety of conditions during planktonic growth. It is hypothesized that these genes encode holins and antiholins, respectively, and may serve as molecular control elements of bacterial cell lysis. To examine the biological role of cell death and lysis, we studied the impact of the cidA mutation on biofilm development. Interestingly, this mutation had a dramatic impact on biofilm morphology and adherence. The cidA mutant (KB1050) biofilm exhibited a rougher appearance compared with the parental strain (UAMS-1) and was less adherent. Propidium iodide staining revealed that KB1050 accumulated more dead cells within the biofilm population relative to UAMS-1, indicative of reduced cell lysis. In agreement with this finding, quantitative real-time PCR experiments demonstrated the presence of 5-fold less genomic DNA in the KB1050 biofilm relative to UAMS-1. Furthermore, treatment of the UAMS-1 biofilm with DNase I caused extensive cell detachment, whereas similar treatment of the KB1050 biofilm had only a modest effect. These results demonstrate that cidA-controlled cell lysis plays a significant role during biofilm development and that released genomic DNA is an important structural component of S. aureus biofilm.
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              Regulatory circuitry governing fungal development, drug resistance, and disease.

              Pathogenic fungi have become a leading cause of human mortality due to the increasing frequency of fungal infections in immunocompromised populations and the limited armamentarium of clinically useful antifungal drugs. Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus are the leading causes of opportunistic fungal infections. In these diverse pathogenic fungi, complex signal transduction cascades are critical for sensing environmental changes and mediating appropriate cellular responses. For C. albicans, several environmental cues regulate a morphogenetic switch from yeast to filamentous growth, a reversible transition important for virulence. Many of the signaling cascades regulating morphogenesis are also required for cells to adapt and survive the cellular stresses imposed by antifungal drugs. Many of these signaling networks are conserved in C. neoformans and A. fumigatus, which undergo distinct morphogenetic programs during specific phases of their life cycles. Furthermore, the key mechanisms of fungal drug resistance, including alterations of the drug target, overexpression of drug efflux transporters, and alteration of cellular stress responses, are conserved between these species. This review focuses on the circuitry regulating fungal morphogenesis and drug resistance and the impact of these pathways on virulence. Although the three human-pathogenic fungi highlighted in this review are those most frequently encountered in the clinic, they represent a minute fraction of fungal diversity. Exploration of the conservation and divergence of core signal transduction pathways across C. albicans, C. neoformans, and A. fumigatus provides a foundation for the study of a broader diversity of pathogenic fungi and a platform for the development of new therapeutic strategies for fungal disease.
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                Author and article information

                Journal
                J Oral Microbiol
                J Oral Microbiol
                ZJOM
                zjom20
                Journal of Oral Microbiology
                Taylor & Francis
                2000-2297
                2018
                04 June 2018
                : 10
                : 1
                : 1476644
                Affiliations
                [a ] Department of Cariology, Operative Dentistry and Dental Public Health, Indiana University– Purdue University Indianapolis, School of Dentistry , Indianapolis, IN, USA
                [b ] Department of Dental Materials and Prosthodontics, São Paulo State University (Unesp), School of Dentistry , Araraquara, São Paulo, Brazil
                Author notes
                CONTACT Ana Cláudia Pavarina pavarina@ 123456foar.unesp.br Department of Dental Materials and Prosthodontics, São Paulo State University (Unesp), School of Dentistry , Araraquara, São Paulo, Brazil
                Author information
                http://orcid.org/0000-0002-2138-1223
                http://orcid.org/0000-0002-7916-1557
                http://orcid.org/0000-0002-9575-7625
                http://orcid.org/0000-0002-9231-1994
                Article
                1476644
                10.1080/20002297.2018.1476644
                5990947
                29887974
                66e93d92-803e-4557-aab6-bab04d2259da
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 January 2018
                : 07 May 2018
                Page count
                Figures: 11, Tables: 1, References: 59, Pages: 13
                Funding
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico 10.13039/501100003593
                Award ID: 465360/2014-9
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo 10.13039/501100001807
                Award ID: 2014/50857-8
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo 10.13039/501100001807
                Award ID: 2014/18804-1
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo 10.13039/501100001807
                Award ID: 2013/07276-1
                This work was supported by the São Paulo Research Foundation: [FAPESP, Grant Numbers 2014/18804-1 and 2013/07276-1] and by the National Institute in Basic Optics and Applied to Life Sciences: [FAPESP Grant Number 2014/50857-8 and National Counsel of Technological and Scientific Development – CNPq Grant Number 465360/2014-9].
                Categories
                Original Article

                Microbiology & Virology
                biofilm,candida albicans,candida glabrata,extracellular matrix,fluconazole,fluconazole-resistant

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