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      Pathogenesis and Clinical Relevance of Candida Biofilms in Vulvovaginal Candidiasis

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          Abstract

          The ability of Candida spp. to form biofilms is crucial for its pathogenicity, and thus, it should be considered an important virulence factor in vulvovaginal candidiasis (VVC) and recurrent VVC (RVVC). Its ability to generate biofilms is multifactorial and is generally believed to depend on the site of infection, species and strain involved, and the microenvironment in which the infection develops. Therefore, both cell surface proteins, such as Hwp1, Als1, and Als2, and the cell wall-related protein, Sun41, play a critical role in the adhesion and virulence of the biofilm. Immunological and pharmacological approaches have identified the NLRP3 inflammasome as a crucial molecular factor contributing to host immunopathology. In this context, we have earlier shown that Candida albicans associated with hyphae-secreted aspartyl proteinases (specifically SAP4-6) contribute to the immunopathology of the disease. Transcriptome profiling has revealed that non-coding transcripts regulate protein synthesis post-transcriptionally, which is important for the growth of Candida spp. Other studies have employed RNA sequencing to identify differences in the 1,245 Candida genes involved in surface and invasive cellular metabolism regulation. In vitro systems allow the simultaneous processing of a large number of samples, making them an ideal screening technique for estimating various physicochemical parameters, testing the activity of antimicrobial agents, and analyzing genes involved in biofilm formation and regulation ( in situ) in specific strains. Murine VVC models are used to study C. albicans infection, especially in trials of novel treatments and to understand the cause(s) for resistance to conventional therapeutics. This review on the clinical relevance of Candida biofilms in VVC focuses on important advances in its genomics, transcriptomics, and proteomics. Moreover, recent experiments on the influence of biofilm formation on VVC or RVVC pathogenesis in laboratory animals have been discussed. A clear elucidation of one of the pathogenesis mechanisms employed by Candida biofilms in vulvovaginal candidiasis and its applications in clinical practice represents the most significant contribution of this manuscript.

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          Most cited references202

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          Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement

          Systematic reviews should build on a protocol that describes the rationale, hypothesis, and planned methods of the review; few reviews report whether a protocol exists. Detailed, well-described protocols can facilitate the understanding and appraisal of the review methods, as well as the detection of modifications to methods and selective reporting in completed reviews. We describe the development of a reporting guideline, the Preferred Reporting Items for Systematic reviews and Meta-Analyses for Protocols 2015 (PRISMA-P 2015). PRISMA-P consists of a 17-item checklist intended to facilitate the preparation and reporting of a robust protocol for the systematic review. Funders and those commissioning reviews might consider mandating the use of the checklist to facilitate the submission of relevant protocol information in funding applications. Similarly, peer reviewers and editors can use the guidance to gauge the completeness and transparency of a systematic review protocol submitted for publication in a journal or other medium.
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            The biofilm matrix.

            The microorganisms in biofilms live in a self-produced matrix of hydrated extracellular polymeric substances (EPS) that form their immediate environment. EPS are mainly polysaccharides, proteins, nucleic acids and lipids; they provide the mechanical stability of biofilms, mediate their adhesion to surfaces and form a cohesive, three-dimensional polymer network that interconnects and transiently immobilizes biofilm cells. In addition, the biofilm matrix acts as an external digestive system by keeping extracellular enzymes close to the cells, enabling them to metabolize dissolved, colloidal and solid biopolymers. Here we describe the functions, properties and constituents of the EPS matrix that make biofilms the most successful forms of life on earth.
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              Vulvovaginal candidosis.

              Despite therapeutic advances, vulvovaginal candidosis remains a common problem worldwide, affecting all strata of society. Understanding of anti-candida host defence mechanisms in the vagina has developed slowly and, despite a growing list of recognised risk factors, a fundamental grasp of pathogenic mechanisms continues to elude us. The absence of rapid, simple, and inexpensive diagnostic tests continues to result in both overdiagnosis and underdiagnosis of vulvovaginal candidosis. I review the epidemiology and pathogenesis of this infection, and also discuss management strategies.
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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
                11 November 2020
                2020
                : 11
                : 544480
                Affiliations
                [1] 1Efficiency, Quality, and Costs in Health Services Research Group (EFISALUD), Health Research Institute, SERGAS-UVIGO , Vigo, Spain
                [2] 2Department of Dermatology, Hospital do Meixoeiro and University of Vigo , Vigo, Spain
                [3] 3European Women’s Dermatologic and Venereologic Society , Tui, Spain
                [4] 4Psychodermatology Task Force of the Ibero-Latin American College of Dermatology (CILAD) , Buenos Aires, Argentina
                [5] 5Unidad de Investigación, Hospital Regional de Alta Especialidad de Ixtapaluca , Ixtapaluca, Mexico
                [6] 6Department of Molecular Diagnosis (Array & NGS Division), Institute of Cellular and Molecular Studies , Lugo, Spain
                [7] 7Section of Mycology, Department of Dermatology, Manuel Gea González hospital , Mexico City, Mexico
                [8] 8Department of Dermatology, University of Naples Federico II , Naples, Italy
                [9] 9Department of Dermatology, University of Medicine, Tirana , Tirana, Albania
                [10] 10Department of Dermatology, Faculty of Medicine, Ain Shams University , Cairo, Egypt
                Author notes

                Edited by: Juliana Campos Junqueira, São Paulo State University, Brazil

                Reviewed by: Rohitashw Kumar, University at Buffalo, United States; Noelly Queiroz Ribeiro, Federal University of Minas Gerais, Brazil

                This article was submitted to Fungi and Their Interactions, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2020.544480
                7686049
                33262741
                2604904d-d9e9-42f4-8f6e-fe8010f19698
                Copyright © 2020 Rodríguez-Cerdeira, Martínez-Herrera, Carnero-Gregorio, López-Barcenas, Fabbrocini, Fida, El-Samahy and González-Cespón.

                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
                : 20 March 2020
                : 23 October 2020
                Page count
                Figures: 3, Tables: 5, Equations: 0, References: 202, Pages: 23, Words: 0
                Categories
                Microbiology
                Review

                Microbiology & Virology
                vulvovaginal candidiasis,candida spp.,biofilm models,proteomic,genomic,new anti-candida targets

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