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Intestinal fungal-host interactions in promoting and maintaining health

https://doi.org/10.1016/j.chom.2024.09.010

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What this work says

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

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The mammalian mycobiome: A complex system in a dynamic relationship with the host

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C-Type Lectin Receptors in Antifungal Immunity

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Fungi in Gastrointestinal Tracts of Human and Mice: from Community to Functions

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Candida spp. in Human Intestinal Health and Disease: More than a Gut Feeling

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The Role of Early Life Gut Mycobiome on Child Health

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Human gut mycobiota tune immunity via CARD9-dependent induction of anti-fungal IgG antibodies

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SnapShot: Microbiota effects on host physiology

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Mucosal fungi promote gut barrier function and social behavior via Type 17 immunity

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Design, construction, and in vivo augmentation of a complex gut microbiome

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Phage therapy: From biological mechanisms to future directions

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A genomic compendium of cultivated human gut fungi characterizes the gut mycobiome and its relevance to common diseases

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Pathogen size alters C-type lectin receptor signaling in dendritic cells to influence CD4 Th9 cell differentiation

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Gut Dysbiosis Promotes M2 Macrophage Polarization and Allergic Airway Inflammation via Fungi-Induced PGE2

inferredcites →https://doi.org/10.1016/j.chom.2014.03.008openalex-snapshot

Fungal Engagement of the C-Type Lectin Mincle Suppresses Dectin-1-Induced Antifungal Immunity

inferredcites →https://doi.org/10.1016/j.chom.2015.07.003openalex-snapshot

Inhibition of Dectin-1 Signaling Ameliorates Colitis by Inducing Lactobacillus-Mediated Regulatory T Cell Expansion in the Intestine

inferredcites →https://doi.org/10.1016/j.chom.2016.05.003openalex-snapshot

Immunological Consequences of Intestinal Fungal Dysbiosis

inferredcites →https://doi.org/10.1016/j.chom.2017.10.013openalex-snapshot

Commensal Fungi Recapitulate the Protective Benefits of Intestinal Bacteria

inferredcites →https://doi.org/10.1016/j.chom.2019.01.007openalex-snapshot

Malassezia Is Associated with Crohn’s Disease and Exacerbates Colitis in Mouse Models

inferredcites →https://doi.org/10.1016/j.chom.2019.01.008openalex-snapshot

Expansion of Bacteriophages Is Linked to Aggravated Intestinal Inflammation and Colitis

inferredcites →https://doi.org/10.1016/j.chom.2019.02.004openalex-snapshot

Commensal Candida albicans Positively Calibrates Systemic Th17 Immunological Responses

inferredcites →https://doi.org/10.1016/j.chom.2020.02.015openalex-snapshot

Altered Immunity of Laboratory Mice in the Natural Environment Is Associated with Fungal Colonization

inferredcites →https://doi.org/10.1016/j.chom.2020.03.001openalex-snapshot

Rewilding Nod2 and Atg16l1 Mutant Mice Uncovers Genetic and Environmental Contributions to Microbial Responses and Immune Cell Composition

inferredcites →https://doi.org/10.1016/j.chom.2021.02.009openalex-snapshot

Microbiota-antibody interactions that regulate gut homeostasis

inferredcites →https://doi.org/10.1016/j.chom.2022.04.005openalex-snapshot

Supplementation with a probiotic mixture accelerates gut microbiome maturation and reduces intestinal inflammation in extremely preterm infants

inferredcites →https://doi.org/10.1016/j.coi.2022.102177openalex-snapshot

Gut microbiome-mediated regulation of neuroinflammation

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Anaerobic Bacteria Grow within Candida albicans Biofilms and Induce Biofilm Formation in Suspension Cultures

inferredcites →https://doi.org/10.1016/j.cub.2020.09.027openalex-snapshot

Gut Bacteria Shape Intestinal Microhabitats Occupied by the Fungus Candida albicans

inferredcites →https://doi.org/10.1016/j.cub.2022.01.049openalex-snapshot

Mycoviruses

inferredcites →https://doi.org/10.1016/j.immuni.2023.11.003openalex-snapshot

Intestinal microbiota-specific Th17 cells possess regulatory properties and suppress effector T cells via c-MAF and IL-10

inferredcites →https://doi.org/10.1016/j.isci.2024.110412openalex-snapshot

The gut mycobiome signatures in long-lived populations

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Host–microbe interactions: Malassezia and human skin

inferredcites →https://doi.org/10.1016/j.mib.2019.09.010openalex-snapshot

Gut mycobiota under scrutiny: fungal symbionts or environmental transients?

inferredcites →https://doi.org/10.1016/j.micpath.2019.103619openalex-snapshot

Binary interactions between the yeast Candida albicans and two gut-associated Bacteroides species

inferredcites →https://doi.org/10.1016/j.xcrm.2023.100928openalex-snapshot

Maturational patterns of the infant gut mycobiome are associated with early-life body mass index

inferredcites →https://doi.org/10.1038/218542a0openalex-snapshot

Viruses in Fungi and Interferon Stimulation

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Creating and characterizing communities of human gut microbes in gnotobiotic mice

inferredcites →https://doi.org/10.1038/nature06244openalex-snapshot

The Human Microbiome Project

inferredcites →https://doi.org/10.1038/nature17655openalex-snapshot

Normalizing the environment recapitulates adult human immune traits in laboratory mice

inferredcites →https://doi.org/10.1038/nrmicro.2016.157openalex-snapshot

Candida albicans cell-type switching and functional plasticity in the mammalian host

inferredcites →https://doi.org/10.1038/nrmicro1347openalex-snapshot

Yeast viral killer toxins: lethality and self-protection

inferredcites →https://doi.org/10.1038/s41390-023-02471-yopenalex-snapshot

Development of gut mycobiome in infants and young children: a prospective cohort study

inferredcites →https://doi.org/10.1038/s41467-020-16431-1openalex-snapshot

Intestinal fungi are causally implicated in microbiome assembly and immune development in mice

inferredcites →https://doi.org/10.1038/s41467-021-26390-wopenalex-snapshot

A small molecule produced by Lactobacillus species blocks Candida albicans filamentation by inhibiting a DYRK1-family kinase

inferredcites →https://doi.org/10.1038/s41467-022-30661-5openalex-snapshot

Lactobacillus rhamnosus colonisation antagonizes Candida albicans by forcing metabolic adaptations that compromise pathogenicity

inferredcites →https://doi.org/10.1038/s41467-022-30686-wopenalex-snapshot

Temporal changes in gastrointestinal fungi and the risk of autoimmunity during early childhood: the TEDDY study

inferredcites →https://doi.org/10.1038/s41467-022-34722-7openalex-snapshot

PD-L1 negatively regulates antifungal immunity by inhibiting neutrophil release from bone marrow

inferredcites →https://doi.org/10.1038/s41564-021-00983-zopenalex-snapshot

Mycobiota-induced IgA antibodies regulate fungal commensalism in the gut and are dysregulated in Crohn’s disease

inferredcites →https://doi.org/10.1038/s41575-023-00816-wopenalex-snapshot

Commensal fungi in intestinal health and disease

inferredcites →https://doi.org/10.1038/s41579-020-00460-0openalex-snapshot

The gut microbiota–brain axis in behaviour and brain disorders

inferredcites →https://doi.org/10.1038/s41579-022-00720-1openalex-snapshot

Tackling the emerging threat of antifungal resistance to human health

inferredcites →https://doi.org/10.1038/s41579-022-00768-zopenalex-snapshot

Microbiota succession throughout life from the cradle to the grave

inferredcites →https://doi.org/10.1038/s41579-022-00796-9openalex-snapshot

Architecture of the dynamic fungal cell wall

inferredcites →https://doi.org/10.1038/s41586-021-03241-8openalex-snapshot

Multi-kingdom ecological drivers of microbiota assembly in preterm infants

inferredcites →https://doi.org/10.1038/s41586-021-03669-yopenalex-snapshot

Microbiota regulate social behaviour via stress response neurons in the brain

inferredcites →https://doi.org/10.1038/s41586-021-03722-wopenalex-snapshot

Adaptive immunity induces mutualism between commensal eukaryotes

inferredcites →https://doi.org/10.1038/s41586-022-04396-8openalex-snapshot

A gut-derived metabolite alters brain activity and anxiety behaviour in mice

inferredcites →https://doi.org/10.1038/s41586-022-04502-wopenalex-snapshot

Immune regulation by fungal strain diversity in inflammatory bowel disease

inferredcites →https://doi.org/10.1038/s41586-022-05546-8openalex-snapshot

Questioning the fetal microbiome illustrates pitfalls of low-biomass microbial studies

inferredcites →https://doi.org/10.1038/s41586-024-07499-6openalex-snapshot

Profiling phagosome proteins identifies PD-L1 as a fungal-binding receptor

inferredcites →https://doi.org/10.1038/s41598-019-44579-4openalex-snapshot

Vaginal lactobacilli inhibit growth and hyphae formation of Candida albicans

inferredcites →https://doi.org/10.1073/pnas.0711918105openalex-snapshot

The PD-1/PD-L costimulatory pathway critically affects host resistance to the pathogenic fungus Histoplasma capsulatum

inferredcites →https://doi.org/10.1073/pnas.0805177106openalex-snapshot

C-type lectin Mincle is an activating receptor for pathogenic fungus, Malassezia

inferredcites →https://doi.org/10.1073/pnas.1102938108openalex-snapshot

Extensive personal human gut microbiota culture collections characterized and manipulated in gnotobiotic mice

inferredcites →https://doi.org/10.1074/jbc.m113.547034openalex-snapshot

Chemical Organization of the Cell Wall Polysaccharide Core of Malassezia restricta

inferredcites →https://doi.org/10.1084/jem.20082818openalex-snapshot

Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection

inferredcites →https://doi.org/10.1093/cid/ciw038openalex-snapshot

Probiotics as Antifungals in Mucosal Candidiasis

inferredcites →https://doi.org/10.1093/femspd/fty038openalex-snapshot

Secondary bile acids inhibit Candida albicans growth and morphogenesis

inferredcites →https://doi.org/10.1093/femsre/fuaa060openalex-snapshot

The impact of the Fungus-Host-Microbiota interplay uponCandida albicansinfections: current knowledge and new perspectives

inferredcites →https://doi.org/10.1093/femsyr/foad046openalex-snapshot

The prevalence of killer yeasts and double-stranded RNAs in the budding yeast Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1093/femsyr/foz008openalex-snapshot

Anti-Candidaactivity of beneficial vaginal lactobacilli inin vitroassays and in a murine experimental model

inferredcites →https://doi.org/10.1093/g3journal/jkac224openalex-snapshot

The future of fungi: threats and opportunities

inferredcites →https://doi.org/10.1093/ibd/izad289openalex-snapshot

Fungal Microbiota Composition in Inflammatory Bowel Disease Patients: Characterization in Different Phenotypes and Correlation With Clinical Activity and Disease Course

inferredcites →https://doi.org/10.1093/mmy/myae004openalex-snapshot

The intestinal commensal fungus Wallemia mellicola enhances asthma in mice through Dectin-2

inferredcites →https://doi.org/10.1096/fj.201901436rropenalex-snapshot

Fungi form interkingdom microbial communities in the primordial human gut that develop with gestational age

inferredcites →https://doi.org/10.1097/mog.0000000000000483openalex-snapshot

Mucosal immune responses to fungi and the implications for inflammatory bowel disease

inferredcites →https://doi.org/10.1111/j.1365-2249.2003.02392.xopenalex-snapshot

Anti-Saccharomyces cerevisiae antibodies (ASCA) in Crohn's disease are associated with disease severity but not NOD2/CARD15 mutations

inferredcites →https://doi.org/10.1126/science.1221789openalex-snapshot

Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis

inferredcites →https://doi.org/10.1126/science.1223490openalex-snapshot

Interactions Between the Microbiota and the Immune System

inferredcites →https://doi.org/10.1126/science.aat0537openalex-snapshot

Experimental evolution of a fungal pathogen into a gut symbiont

inferredcites →https://doi.org/10.1126/science.abj2972openalex-snapshot

Robust variation in infant gut microbiome assembly across a spectrum of lifestyles

inferredcites →https://doi.org/10.1126/science.abq3178openalex-snapshot

Peptide YY: A Paneth cell antimicrobial peptide that maintains Candida gut commensalism

inferredcites →https://doi.org/10.1126/scitranslmed.aad0917openalex-snapshot

Natural history of the infant gut microbiome and impact of antibiotic treatment on bacterial strain diversity and stability

inferredcites →https://doi.org/10.1126/scitranslmed.aaf9044openalex-snapshot

A member of the gut mycobiota modulates host purine metabolism exacerbating colitis in mice

inferredcites →https://doi.org/10.1128/aem.02994-18openalex-snapshot

Mycobiome Profiles in Breast Milk from Healthy Women Depend on Mode of Delivery, Geographic Location, and Interaction with Bacteria

inferredcites →https://doi.org/10.1128/cmr.10.3.369openalex-snapshot

Yeast killer systems

inferredcites →https://doi.org/10.1128/mbio.01534-20openalex-snapshot

A Novel Mycovirus Evokes Transcriptional Rewiring in the Fungus Malassezia and Stimulates Beta Interferon Production in Macrophages

inferredcites →https://doi.org/10.1128/mbio.02123-20openalex-snapshot

Antimicrobial Peptides: a New Frontier in Antifungal Therapy

inferredcites →https://doi.org/10.1128/msphere.00092-18openalex-snapshot

Investigating Colonization of the Healthy Adult Gastrointestinal Tract by Fungi

inferredcites →https://doi.org/10.1128/msphere.00558-19openalex-snapshot

Age-Related Variation of Bacterial and Fungal Communities in Different Body Habitats across the Young, Elderly, and Centenarians in Sardinia

inferredcites →https://doi.org/10.1128/msystems.00140-17openalex-snapshot

Development of the Human Mycobiome over the First Month of Life and across Body Sites

inferredcites →https://doi.org/10.1136/adc.69.5_spec_no.483openalex-snapshot

Enteral feeding of premature infants with Lactobacillus GG.

inferredcites →https://doi.org/10.1136/gutjnl-2021-326298openalex-snapshot

Mapping the human gut mycobiome in middle-aged and elderly adults: multiomics insights and implications for host metabolic health

inferredcites →https://doi.org/10.1146/annurev-pathol-052016-100342openalex-snapshot

Immunity to Commensal Fungi: Detente and Disease

inferredcites →https://doi.org/10.1146/annurev-virology-091919-101238openalex-snapshot

Bacteriophage-Bacteria Interactions in the Gut: From Invertebrates to Mammals

inferredcites →https://doi.org/10.1172/jci161593openalex-snapshot

Antigen specificity and cross-reactivity drive functionally diverse anti–Aspergillus fumigatus T cell responses in cystic fibrosis

inferredcites →https://doi.org/10.1186/s40168-017-0319-xopenalex-snapshot

Early gut mycobiota and mother-offspring transfer

inferredcites →https://doi.org/10.1186/s40168-017-0373-4openalex-snapshot

The gut mycobiome of the Human Microbiome Project healthy cohort

inferredcites →https://doi.org/10.1186/s40168-020-00899-6openalex-snapshot

Antibiotics create a shift from mutualism to competition in human gut communities with a longer-lasting impact on fungi than bacteria

inferredcites →https://doi.org/10.1186/s40168-022-01273-4openalex-snapshot

Deletion of both Dectin-1 and Dectin-2 affects the bacterial but not fungal gut microbiota and susceptibility to colitis in mice

inferredcites →https://doi.org/10.1186/s40168-023-01586-yopenalex-snapshot

Enterotypes of the human gut mycobiome

inferredcites →https://doi.org/10.1371/journal.pone.0131220openalex-snapshot

Isolation of Vaginal Lactobacilli and Characterization of Anti-Candida Activity

inferredcites →https://doi.org/10.1371/journal.ppat.1004050openalex-snapshot

Fungal Chitin Dampens Inflammation through IL-10 Induction Mediated by NOD2 and TLR9 Activation

inferredcites →https://doi.org/10.1371/journal.ppat.1007260openalex-snapshot

Expansion of commensal fungus Wallemia mellicola in the gastrointestinal mycobiota enhances the severity of allergic airway disease in mice

inferredcites →https://doi.org/10.21203/rs.3.rs-3961709/v1openalex-snapshot

Aspergillus dsRNA virus drives fungal fitness and pathogenicity in the mammalian host

inferredcites →https://doi.org/10.3389/fcimb.2020.583418openalex-snapshot

The Fungal Microbiome and Asthma

inferredcites →https://doi.org/10.3389/fcimb.2022.1020608openalex-snapshot

Inseparable companions: Fungal viruses as regulators of fungal fitness and host adaptation

inferredcites →https://doi.org/10.3389/fimmu.2022.1018202openalex-snapshot

Checkpoint inhibitors as immunotherapy for fungal infections: Promises, challenges, and unanswered questions

inferredcites →https://doi.org/10.3389/fmicb.2016.01227openalex-snapshot

Age and Gender Affect the Composition of Fungal Population of the Human Gastrointestinal Tract

inferredcites →https://doi.org/10.3389/fmicb.2020.01994openalex-snapshot

Phenotypic Variability in a Coinfection With Three Independent Candida parapsilosis Lineages

inferredcites →https://doi.org/10.3390/jof6040243openalex-snapshot

Let’s Get Physical: Bacterial-Fungal Interactions and Their Consequences in Agriculture and Health

inferredcites →https://doi.org/10.3390/jof8040328openalex-snapshot

The Effect of Antibiotics on the Infant Gut Fungal Microbiota

inferredcites →https://doi.org/10.3390/jof9070718openalex-snapshot

Delivery Mode and Perinatal Antibiotics Influence the Infant Gut Bacteriome and Mycobiome: A Network Analysis

inferredcites →https://doi.org/10.3920/bm2019.0158openalex-snapshot

Human milk mycobiota composition: relationship with gestational age, delivery mode, and birth weight

What points at this work

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

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Characterization of fungal and bacterial Dysbiosis in Crohn's Disease Patients with Intestinal Fibrosis

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