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Intersection of phosphate transport, oxidative stress and TOR signalling in Candida albicans virulence

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/yea.738openalex-snapshot

Cassettes for PCR‐mediated construction of green, yellow, and cyan fluorescent protein fusions in Candida albicans

inferredcites →https://doi.org/10.1007/s00018-016-2294-yopenalex-snapshot

Control of Candida albicans morphology and pathogenicity by post-transcriptional mechanisms

inferredcites →https://doi.org/10.1007/s00204-015-1520-yopenalex-snapshot

Interactions between mitochondrial reactive oxygen species and cellular glucose metabolism

inferredcites →https://doi.org/10.1007/s00775-013-1045-xopenalex-snapshot

Species-specific activation of Cu/Zn SOD by its CCS copper chaperone in the pathogenic yeast Candida albicans

inferredcites →https://doi.org/10.1007/s10863-017-9695-yopenalex-snapshot

H+-dependent inorganic phosphate uptake in Trypanosoma brucei is influenced by myo-inositol transporter

inferredcites →https://doi.org/10.1007/s12038-014-9435-yopenalex-snapshot

Conservation of PHO pathway in ascomycetes and the role of Pho84

inferredcites →https://doi.org/10.1007/s12275-015-4727-yopenalex-snapshot

Deletion analysis of LSm, FDF, and YjeF domains of Candida albicans Edc3 in hyphal growth and oxidative-stress response

inferredcites →https://doi.org/10.1007/s40265-013-0133-0openalex-snapshot

Therapeutic Options for Visceral Leishmaniasis

inferredcites →https://doi.org/10.1016/0002-9343(81)90259-xopenalex-snapshot

Fungal infection in chronic granulomatous disease

inferredcites →https://doi.org/10.1016/0003-9969(80)90147-8openalex-snapshot

The prevalence and intra-oral distribution of Candida albicans in man

inferredcites →https://doi.org/10.1016/j.bbagen.2012.11.017openalex-snapshot

Transport of inorganic phosphate in Leishmania infantum and compensatory regulation at low inorganic phosphate concentration

inferredcites →https://doi.org/10.1016/j.bbagen.2013.04.034openalex-snapshot

Inorganic phosphate uptake in Trypanosoma cruzi is coupled to K+ cycling and to active Na+ extrusion

inferredcites →https://doi.org/10.1016/j.bbagen.2014.03.014openalex-snapshot

Inorganic phosphate uptake in unicellular eukaryotes

inferredcites →https://doi.org/10.1016/j.cmet.2011.03.018openalex-snapshot

Regulation of Yeast Chronological Life Span by TORC1 via Adaptive Mitochondrial ROS Signaling

inferredcites →https://doi.org/10.1016/j.febslet.2012.01.036openalex-snapshot

Phosphate homeostasis in the yeast Saccharomyces cerevisiae, the key role of the SPX domain‐containing proteins

inferredcites →https://doi.org/10.1016/j.fgb.2018.04.004openalex-snapshot

Evolutionary conservation of a core fungal phosphate homeostasis pathway coupled to development in Blastocladiella emersonii

inferredcites →https://doi.org/10.1016/j.molp.2016.08.011openalex-snapshot

Arbuscular Mycorrhizal Symbiosis Requires a Phosphate Transceptor in the Gigaspora margarita Fungal Symbiont

inferredcites →https://doi.org/10.1016/j.tim.2004.05.008openalex-snapshot

The distinct morphogenic states of Candida albicans

inferredcites →https://doi.org/10.1016/s0092-8674(00)80358-xopenalex-snapshot

Nonfilamentous C. albicans Mutants Are Avirulent

inferredcites →https://doi.org/10.1038/nature18849openalex-snapshot

Interactions between the microbiota and pathogenic bacteria in the gut

inferredcites →https://doi.org/10.1038/ng.605openalex-snapshot

Systematic screens of a Candida albicans homozygous deletion library decouple morphogenetic switching and pathogenicity

inferredcites →https://doi.org/10.1038/nprot.2012.011openalex-snapshot

Mouse model of oropharyngeal candidiasis

inferredcites →https://doi.org/10.1042/bj20112086openalex-snapshot

Mutational analysis of putative phosphate- and proton-binding sites in the Saccharomyces cerevisiae Pho84 phosphate:H+ transceptor and its effect on signalling to the PKA and PHO pathways

inferredcites →https://doi.org/10.1042/bj2370111openalex-snapshot

The effect of the inhibitor diphenylene iodonium on the superoxide-generating system of neutrophils. Specific labelling of a component polypeptide of the oxidase

inferredcites →https://doi.org/10.1042/bj2510887openalex-snapshot

The effect of the NADPH oxidase inhibitor diphenyleneiodonium on aerobic and anaerobic microbicidal activities of human neutrophils

inferredcites →https://doi.org/10.1056/nejmoa1507574openalex-snapshot

Randomized Trial of Benznidazole for Chronic Chagas’ Cardiomyopathy

inferredcites →https://doi.org/10.1073/pnas.0809147105openalex-snapshot

The Candida albicans pescadillo homolog is required for normal hypha-to-yeast morphogenesis and yeast proliferation

inferredcites →https://doi.org/10.1073/pnas.0906546107openalex-snapshot

Transport and signaling through the phosphate-binding site of the yeast Pho84 phosphate transceptor

inferredcites →https://doi.org/10.1073/pnas.1513447112openalex-snapshot

Candida albicans adapts to host copper during infection by swapping metal cofactors for superoxide dismutase

inferredcites →https://doi.org/10.1073/pnas.1617799114openalex-snapshot

Phosphate is the third nutrient monitored by TOR in Candida albicans and provides a target for fungal-specific indirect TOR inhibition

inferredcites →https://doi.org/10.1073/pnas.89.12.5547openalex-snapshot

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters.

inferredcites →https://doi.org/10.1074/jbc.m108095200openalex-snapshot

Candida albicans Expresses an Unusual Cytoplasmic Manganese-containing Superoxide Dismutase (SOD3 Gene Product) upon the Entry and during the Stationary Phase

inferredcites →https://doi.org/10.1074/jbc.m113.494815openalex-snapshot

Essential Role for Vacuolar Acidification in Candida albicans Virulence

inferredcites →https://doi.org/10.1074/jbc.m307413200openalex-snapshot

The Saccharomyces cerevisiae High Affinity Phosphate Transporter Encoded by PHO84 Also Functions in Manganese Homeostasis

inferredcites →https://doi.org/10.1083/jcb.133.4.895openalex-snapshot

Deficiency of Src family kinases p59/61hck and p58c-fgr results in defective adhesion-dependent neutrophil functions.

inferredcites →https://doi.org/10.1084/jem.20102049openalex-snapshot

Mitochondrial reactive oxygen species promote production of proinflammatory cytokines and are elevated in TNFR1-associated periodic syndrome (TRAPS)

inferredcites →https://doi.org/10.1091/mbc.e03-03-0179openalex-snapshot

Superoxide Dismutases in Candida albicans : Transcriptional Regulation and Functional Characterization of the Hyphal-induced SOD5 Gene

inferredcites →https://doi.org/10.1091/mbc.e05-06-0501openalex-snapshot

Role of the Hog1 Stress-activated Protein Kinase in the Global Transcriptional Response to Stress in the Fungal PathogenCandida albicans

inferredcites →https://doi.org/10.1091/mbc.e16-05-0266openalex-snapshot

Pho4 mediates phosphate acquisition inCandida albicansand is vital for stress resistance and metal homeostasis

inferredcites →https://doi.org/10.1093/genetics/134.3.717openalex-snapshot

Isogenic strain construction and gene mapping in Candida albicans.

inferredcites →https://doi.org/10.1099/00221287-148-11-3705openalex-snapshot

Copper- and zinc-containing superoxide dismutase (Cu/ZnSOD) is required for the protection of Candida albicans against oxidative stresses and the expression of its full virulence

inferredcites →https://doi.org/10.1101/cshperspect.a019273openalex-snapshot

The Spectrum of Fungi That Infects Humans

inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04238.xopenalex-snapshot

Rck1 and Rck2 MAPKAP kinases and the HOG pathway are required for oxidative stress resistance

inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04557.xopenalex-snapshot

Granulocytes govern the transcriptional response, morphology and proliferation of Candida albicans in human blood

inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06528.xopenalex-snapshot

Candida albicans cell surface superoxide dismutases degrade host‐derived reactive oxygen species to escape innate immune surveillance

inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07310.xopenalex-snapshot

PhoB regulates both environmental and virulence gene expression in Vibrio cholerae

inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00659.xopenalex-snapshot

Neutrophil extracellular traps capture and kill Candida albicans yeast and hyphal forms

inferredcites →https://doi.org/10.1111/j.1462-5822.2007.00898.xopenalex-snapshot

Differential susceptibility of mitogen-activated protein kinase pathway mutants to oxidative-mediated killing by phagocytes in the fungal pathogen Candida albicans

inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00101.xopenalex-snapshot

The phosphate regulon and bacterial virulence: a regulatory network connecting phosphate homeostasis and pathogenesis

inferredcites →https://doi.org/10.1111/mmi.13130openalex-snapshot

Ribosomal protein S 6 phosphorylation is controlled by TOR and modulated by PKA in C andida albicans

inferredcites →https://doi.org/10.1128/cmr.00005-11openalex-snapshot

Trypanosoma cruzi and Chagas' Disease in the United States

inferredcites →https://doi.org/10.1128/ec.00312-09openalex-snapshot

Global Gene Expression Analysis during Sporulation of the Aquatic Fungus Blastocladiella emersonii

inferredcites →https://doi.org/10.1128/ec.2.2.351-361.2003openalex-snapshot

The Hog1 Mitogen-Activated Protein Kinase Is Essential in the Oxidative Stress Response and Chlamydospore Formation inCandidaalbicans

inferredcites →https://doi.org/10.1128/iai.01607-14openalex-snapshot

Defects in Phosphate Acquisition and Storage Influence Virulence of Cryptococcus neoformans

inferredcites →https://doi.org/10.1128/jb.98.3.996-1004.1969openalex-snapshot

Interaction ofCandida albicanswith Human Leukocytes and Serum

inferredcites →https://doi.org/10.1128/mbio.01649-14openalex-snapshot

Identification of Aph1, a Phosphate-Regulated, Secreted, and Vacuolar Acid Phosphatase in Cryptococcus neoformans

inferredcites →https://doi.org/10.1128/mcb.00156-16openalex-snapshot

Oma1 Links Mitochondrial Protein Quality Control and TOR Signaling To Modulate Physiological Plasticity and Cellular Stress Responses

inferredcites →https://doi.org/10.1128/msphere.00381-16openalex-snapshot

Pho4 Is Essential for Dissemination of Cryptococcus neoformans to the Host Brain by Promoting Phosphate Uptake and Growth at Alkaline pH

inferredcites →https://doi.org/10.1139/w2012-090openalex-snapshot

Phosphate limitation induces sporulation in the chytridiomyceteBlastocladiella emersonii

inferredcites →https://doi.org/10.1146/annurev-genet-120213-092421openalex-snapshot

Gastrointestinal Microbiota–Mediated Control of Enteric Pathogens

inferredcites →https://doi.org/10.1172/jci106114openalex-snapshot

Leukocyte myeloperoxidase deficiency and disseminated candidiasis: the role of myeloperoxidase in resistance to Candida infection

inferredcites →https://doi.org/10.1182/blood-2014-01-551473openalex-snapshot

Two independent killing mechanisms of Candida albicans by human neutrophils: evidence from innate immunity defects

inferredcites →https://doi.org/10.1182/blood.v70.5.1233.1233openalex-snapshot

The HL-60 promyelocytic leukemia cell line: proliferation, differentiation, and cellular oncogene expression

inferredcites →https://doi.org/10.1186/1710-1492-2-3-98openalex-snapshot

Mechanisms of Degranulation in Neutrophils

inferredcites →https://doi.org/10.1371/journal.pone.0027434openalex-snapshot

Wild-Type Drosophila melanogaster as a Model Host to Analyze Nitrogen Source Dependent Virulence of Candida albicans

inferredcites →https://doi.org/10.1371/journal.ppat.0040035openalex-snapshot

Mucosal Damage and Neutropenia Are Required for Candida albicans Dissemination

inferredcites →https://doi.org/10.1371/journal.ppat.1005295openalex-snapshot

SOD Enzymes and Microbial Pathogens: Surviving the Oxidative Storm of Infection

inferredcites →https://doi.org/10.1371/journal.ppat.1006763openalex-snapshot

Candida albicans FRE8 encodes a member of the NADPH oxidase family that produces a burst of ROS during fungal morphogenesis

inferredcites →https://doi.org/10.1534/genetics.111.133306openalex-snapshot

Regulation of Amino Acid, Nucleotide, and Phosphate Metabolism in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.3389/fmicb.2015.00402openalex-snapshot

The Pho regulon: a huge regulatory network in bacteria

inferredcites →https://doi.org/10.3389/fmicb.2015.00984openalex-snapshot

Fungal association and utilization of phosphate by plants: success, limitations, and future prospects

inferredcites →https://doi.org/10.3390/microorganisms5030048openalex-snapshot

Phosphate Acquisition and Virulence in Human Fungal Pathogens

inferredcites →https://doi.org/10.3852/11-229openalex-snapshot

Fresh perspectives on the roles of arbuscular mycorrhizal fungi in plant nutrition and growth

inferredcites →https://doi.org/10.4161/viru.29307openalex-snapshot

Interplay between genetic regulation of phosphate homeostasis and bacterial virulence

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3390/antiox10040572openalex-snapshot

Acetyl-CoA Metabolism and Histone Acetylation in the Regulation of Aging and Lifespan

inferred← citeshttps://doi.org/10.3390/cells8050461openalex-snapshot

The Reduced Level of Inorganic Polyphosphate Mobilizes Antioxidant and Manganese-Resistance Systems in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.3390/ijms27093707openalex-snapshot

Phosphate Acquisition in Protozoan Parasites: Transport Systems, and Extracellular Phosphate-Releasing Enzymatic Activities

inferred← citeshttps://doi.org/10.3390/jof6020040openalex-snapshot

Phosphate in Virulence of Candida albicans and Candida glabrata

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