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      Candida albicans Yeast, Pseudohyphal, and Hyphal Morphogenesis Differentially Affects Immune Recognition

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          Abstract

          Candida albicans is a human opportunist pathogen that can grow as yeast, pseudohyphae, or true hyphae in vitro and in vivo, depending on environmental conditions. Reversible cellular morphogenesis is an important virulence factor that facilitates invasion of host tissues, escape from phagocytes, and dissemination in the blood stream. The innate immune system is the first line of defense against C. albicans infections and is influenced by recognition of wall components that vary in composition in different morphological forms. However, the relationship between cellular morphogenesis and immune recognition of this fungus is not fully understood. We therefore studied various vegetative cell types of C. albicans, singly and in combination, to assess the consequences of cellular morphogenesis on selected immune cytokine outputs from human monocytes. Hyphae stimulated proportionally lower levels of certain cytokines from monocytes per unit of cell surface area than yeast cells, but did not suppress cytokine response when copresented with yeast cells. Pseudohyphal cells induced intermediate cytokine responses. Yeast monomorphic mutants had elevated cytokine responses under conditions that otherwise supported filamentous growth and mutants of yeast and hyphal cells that were defective in cell wall mannosylation or lacking certain hypha-specific cell wall proteins could variably unmask or deplete the surface of immunostimulatory ligands. These observations underline the critical importance of C. albicans morphology and morphology-associated changes in the cell wall composition that affect both immune recognition and pathogenesis.

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          Most cited references69

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          Recognition of microorganisms and activation of the immune response.

          The mammalian immune system has innate and adaptive components, which cooperate to protect the host against microbial infections. The innate immune system consists of functionally distinct 'modules' that evolved to provide different forms of protection against pathogens. It senses pathogens through pattern-recognition receptors, which trigger the activation of antimicrobial defences and stimulate the adaptive immune response. The adaptive immune system, in turn, activates innate effector mechanisms in an antigen-specific manner. The connections between the various immune components are not fully understood, but recent progress brings us closer to an integrated view of the immune system and its function in host defence.
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            Nonfilamentous C. albicans mutants are avirulent.

            Candida albicans and Saccharomyces cerevisiae switch from a yeast to a filamentous form. In Saccharomyces, this switch is controlled by two regulatory proteins, Ste12p and Phd1p. Single-mutant strains, ste12/ste12 or phd1/phd1, are partially defective, whereas the ste12/ste12 phd1/phd1 double mutant is completely defective in filamentous growth and is noninvasive. The equivalent cph1/cph1 efg1/efg1 double mutant in Candida (Cph1p is the Ste12p homolog and Efg1p is the Phd1p homolog) is also defective in filamentous growth, unable to form hyphae or pseudohyphae in response to many stimuli, including serum or macrophages. This Candida cph1/cph1 efg1/efg1 double mutant, locked in the yeast form, is avirulent in a mouse model.
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              Candidalysin is a fungal peptide toxin critical for mucosal infection

              Cytolytic proteins and peptide toxins are classical virulence factors of several bacterial pathogens which disrupt epithelial barrier function, damage cells and activate or modulate host immune responses. Until now human pathogenic fungi were not known to possess such toxins. Here we identify the first fungal cytolytic peptide toxin in the opportunistic pathogen Candida albicans. This secreted toxin directly damages epithelial membranes, triggers a danger response signaling pathway and activates epithelial immunity. Toxin-mediated membrane permeabilization is enhanced by a positively charged C-terminus and triggers an inward current concomitant with calcium influx. C. albicans strains lacking this toxin do not activate or damage epithelial cells and are avirulent in animal models of mucosal infection. We propose the name ‘Candidalysin’ for this cytolytic peptide toxin; a newly identified, critical molecular determinant of epithelial damage and host recognition of the clinically important fungus, C. albicans.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                07 June 2017
                2017
                : 8
                : 629
                Affiliations
                [1] 1Aberdeen Fungal Group, Institute of Medical Sciences, Foresterhill, University of Aberdeen , Aberdeen, United Kingdom
                [2] 2Department of Microbiology and Immunology, Medical School, University of Minnesota , Minneapolis, MN, United States
                [3] 3Departamento de Biología, División de Ciencias Naturales y Exactas, Universidad de Guanajuato , Guanajuato, Mexico
                Author notes

                Edited by: Steven Templeton, Indiana University School of Medicine – Terre Haute, United States

                Reviewed by: Michael K. Mansour, Massachusetts General Hospital, United States; Michail Lionakis, National Institute of Allergy and Infectious Diseases, United States

                *Correspondence: Neil A. R. Gow, n.gow@ 123456abdn.ac.uk

                These authors have contributed equally to this work.

                Specialty section: This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2017.00629
                5461353
                28638380
                dcf4f840-2477-4582-b5af-038e2b4cfda2
                Copyright © 2017 Mukaremera, Lee, Mora-Montes and Gow.

                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) or licensor 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
                : 10 March 2017
                : 12 May 2017
                Page count
                Figures: 6, Tables: 1, Equations: 0, References: 80, Pages: 12, Words: 8864
                Funding
                Funded by: Wellcome Trust 10.13039/100004440
                Award ID: 086827, 075470, 097377, 101873, and 200208
                Funded by: Sixth Framework Programme 10.13039/100011103
                Award ID: ALLFUN FP7/2007 2013, HEALTH-2010-260338
                Funded by: Medical Research Council 10.13039/501100000265
                Award ID: N006364/1
                Categories
                Immunology
                Original Research

                Immunology
                candida albicans,cell wall,cytokine,immune recognition,morphogenesis
                Immunology
                candida albicans, cell wall, cytokine, immune recognition, morphogenesis

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