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Conidial melanin of the human pathogenic fungus Aspergillus fumigatus disrupts cell autonomous defenses in amoebae

https://doi.org/10.1101/730879
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf01716563openalex-snapshot
Macrophage functions in antimicrobial defense
inferredcites →https://doi.org/10.1007/s00253-015-6898-1openalex-snapshot
Identification of the antiphagocytic trypacidin gene cluster in the human-pathogenic fungus Aspergillus fumigatus
inferredcites →https://doi.org/10.1016/j.bbamcr.2005.02.004openalex-snapshot
NADPH oxidase homologs are required for normal cell differentiation and morphogenesis in Dictyostelium discoideum
inferredcites →https://doi.org/10.1016/j.celrep.2020.108017openalex-snapshot
Flotillin-Dependent Membrane Microdomains Are Required for Functional Phagolysosomes against Fungal Infections
inferredcites →https://doi.org/10.1016/j.chom.2015.12.002openalex-snapshot
Aspergillus Cell Wall Melanin Blocks LC3-Associated Phagocytosis to Promote Pathogenicity
inferredcites →https://doi.org/10.1016/j.ijmm.2014.04.009openalex-snapshot
Melanin dependent survival of Apergillus fumigatus conidia in lung epithelial cells
inferredcites →https://doi.org/10.1016/j.imbio.2009.10.002openalex-snapshot
Aspergillus fumigatus Conidial Melanin Modulates Host Cytokine Response
inferredcites →https://doi.org/10.1016/j.mib.2008.05.005openalex-snapshot
Eat, kill or die: when amoeba meets bacteria
inferredcites →https://doi.org/10.1016/s0021-9258(19)38362-0openalex-snapshot
Bleaching of melanin pigments. Role of copper ions and hydrogen peroxide in autooxidation and photooxidation of synthetic dopa-melanin.
inferredcites →https://doi.org/10.1038/nature25974openalex-snapshot
Recognition of DHN-melanin by a C-type lectin receptor is required for immunity to Aspergillus
inferredcites →https://doi.org/10.1038/nrmicro2128openalex-snapshot
Antimicrobial mechanisms of phagocytes and bacterial evasion strategies
inferredcites →https://doi.org/10.1046/j.1462-5822.2002.00228.xopenalex-snapshot
PKSP-dependent reduction of phagolysosome fusion and intracellular kill ofAspergillus fumigatusconidia by human monocyte-derived macrophages
inferredcites →https://doi.org/10.1083/jcb.201009119openalex-snapshot
Actin polymerization driven by WASH causes V-ATPase retrieval and vesicle neutralization before exocytosis
inferredcites →https://doi.org/10.1086/314093openalex-snapshot
Destruction of Fungal Melanins by Ligninases ofPhanerochaete chrysosporiumand Other White Rot Fungi
inferredcites →https://doi.org/10.1091/mbc.e14-05-0967openalex-snapshot
Contrasting phagosome pH regulation and maturation in human M1 and M2 macrophages
inferredcites →https://doi.org/10.1093/gbe/evy011openalex-snapshot
Multiple Roots of Fruiting Body Formation in Amoebozoa
inferredcites →https://doi.org/10.1099/jmm.0.05421-0openalex-snapshot
Production of melanin by Aspergillus fumigatus
inferredcites →https://doi.org/10.1101/582049openalex-snapshot
Dictyostelium discoideum flotillin homologues are essential for phagocytosis and participate in plasma membrane recycling and lysosome biogenesis
inferredcites →https://doi.org/10.1111/1462-2920.12808openalex-snapshot
Virulence determinants of the human pathogenic fungus A spergillus fumigatus protect against soil amoeba predation
inferredcites →https://doi.org/10.1111/1462-2920.14588openalex-snapshot
The different morphologies of yeast and filamentous fungi trigger distinct killing and feeding mechanisms in a fungivorous amoeba
inferredcites →https://doi.org/10.1111/1758-2229.12082openalex-snapshot
Interaction of A spergillus fumigatus conidia with A canthamoeba castellanii parallels macrophage–fungus interactions
inferredcites →https://doi.org/10.1111/cmi.12320openalex-snapshot
The complex roles of NADPH oxidases in fungal infection
inferredcites →https://doi.org/10.1111/cmi.12994openalex-snapshot
The puzzling construction of the conidial outer layer of Aspergillus fumigatus
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00796.xopenalex-snapshot
Phagocytosis of Aspergillus fumigatus conidia by murine macrophages involves recognition by the dectin-1 beta-glucan receptor and Toll-like receptor 2
inferredcites →https://doi.org/10.1111/j.1462-5822.2011.01605.xopenalex-snapshot
Phagocytosis of melanized Aspergillus conidia by macrophages exerts cytoprotective effects by sustained PI3K/Akt signalling
inferredcites →https://doi.org/10.1111/j.1600-0854.2011.01296.xopenalex-snapshot
Dynamin A, Myosin IB and Abp1 Couple Phagosome Maturation to F‐Actin Binding
inferredcites →https://doi.org/10.1126/science.1247136openalex-snapshot
ESCRT Machinery Is Required for Plasma Membrane Repair
inferredcites →https://doi.org/10.1126/science.aar5078openalex-snapshot
Triggered recruitment of ESCRT machinery promotes endolysosomal repair
inferredcites →https://doi.org/10.1126/scitranslmed.3004404openalex-snapshot
Hidden Killers: Human Fungal Infections
inferredcites →https://doi.org/10.1128/mmbr.00024-12openalex-snapshot
Prison Break: Pathogens' Strategies To Egress from Host Cells
inferredcites →https://doi.org/10.1146/annurev.micro.56.012302.160625openalex-snapshot
Menacing Mold: The Molecular Biology of Aspergillus fumigatus
inferredcites →https://doi.org/10.1242/jcs.109.5.1041openalex-snapshot
The vacuolar proton pump of Dictyostelium discoideum: Molecular cloning and analysis of the 100 kDa subunit
inferredcites →https://doi.org/10.1242/jcs.115.14.2893openalex-snapshot
Dynamics of the vacuolar H+-ATPase in the contractile vacuole complex and the endosomal pathway ofDictyosteliumcells
inferredcites →https://doi.org/10.1371/journal.pone.0008585openalex-snapshot
Retrieval of the Vacuolar H+-ATPase from Phagosomes Revealed by Live Cell Imaging
inferredcites →https://doi.org/10.1371/journal.pone.0031223openalex-snapshot
Persistence versus Escape: Aspergillus terreus and Aspergillus fumigatus Employ Different Strategies during Interactions with Macrophages
inferredcites →https://doi.org/10.1371/journal.ppat.1006344openalex-snapshot
Mycobacterium marinum antagonistically induces an autophagic response while repressing the autophagic flux in a TORC1- and ESX-1-dependent manner
inferredcites →https://doi.org/10.1371/journal.ppat.1007501openalex-snapshot
The ESCRT and autophagy machineries cooperate to repair ESX-1-dependent damage at the Mycobacterium-containing vacuole but have opposite impact on containing the infection
inferredcites →https://doi.org/10.3389/fcimb.2018.00108openalex-snapshot
Cryptococcus neoformans Escape From Dictyostelium Amoeba by Both WASH-Mediated Constitutive Exocytosis and Vomocytosis
inferredcites →https://doi.org/10.3389/fimmu.2017.01906openalex-snapshot
Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses
inferredcites →https://doi.org/10.3389/fmicb.2011.00096openalex-snapshot
Conidial Dihydroxynaphthalene Melanin of the Human Pathogenic Fungus Aspergillus fumigatus Interferes with the Host Endocytosis Pathway
inferredcites →https://doi.org/10.3389/fmicb.2012.00440openalex-snapshot
Aspergillus fumigatus melanins: interference with the host endocytosis pathway and impact on virulence
inferredcites →https://doi.org/10.3389/fmicb.2015.01463openalex-snapshot
Fungal Melanin: What do We Know About Structure?
inferredcites →https://doi.org/10.3390/jof3040057openalex-snapshot
Global and Multi-National Prevalence of Fungal Diseases—Estimate Precision
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