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Mucin-degrading gut bacteria promote anti-parasitic immunity

https://doi.org/10.1101/2022.02.28.482289

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What this work says

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

inferredcites →https://doi.org/10.1006/expr.2001.4643openalex-snapshot

Trichuris suis: Detection of Antibacterial Activity in Excretory-Secretory Products from Adults

inferredcites →https://doi.org/10.1007/s00281-012-0348-2openalex-snapshot

Trichuris muris: a model of gastrointestinal parasite infection

inferredcites →https://doi.org/10.1016/j.cell.2016.10.043openalex-snapshot

A Dietary Fiber-Deprived Gut Microbiota Degrades the Colonic Mucus Barrier and Enhances Pathogen Susceptibility

inferredcites →https://doi.org/10.1016/j.exppara.2014.07.009openalex-snapshot

Hymenolepis diminuta: Analysis of the expression of Toll-like receptor genes and protein (TLR3 and TLR9) in the small and large intestines of rats

inferredcites →https://doi.org/10.1016/j.jprot.2011.06.002openalex-snapshot

Proteomic analysis of secretory products from the model gastrointestinal nematode Heligmosomoides polygyrus reveals dominance of Venom Allergen-Like (VAL) proteins

inferredcites →https://doi.org/10.1016/j.molmed.2021.10.004openalex-snapshot

Intestinal mucus barrier: a missing piece of the puzzle in food allergy

inferredcites →https://doi.org/10.1016/j.xpro.2021.100607openalex-snapshot

Constructing a gnotobiotic mouse model with a synthetic human gut microbiome to study host–microbe cross talk

inferredcites →https://doi.org/10.1017/s0031182000072395openalex-snapshot

Acquired immunity toTrichuris murisin the albino laboratory mouse

inferredcites →https://doi.org/10.1038/mi.2017.113openalex-snapshot

Immunity to gastrointestinal nematode infections

inferredcites →https://doi.org/10.1038/nature12240openalex-snapshot

Innate lymphoid cells regulate CD4+ T-cell responses to intestinal commensal bacteria

inferredcites →https://doi.org/10.1038/ncomms14208openalex-snapshot

mTORC2 signalling regulates M2 macrophage differentiation in response to helminth infection and adaptive thermogenesis

inferredcites →https://doi.org/10.1038/s41385-018-0008-5openalex-snapshot

The impact of a helminth-modified microbiome on host immunity

inferredcites →https://doi.org/10.1038/s41564-023-01464-1openalex-snapshot

Akkermansia muciniphila exacerbates food allergy in fibre-deprived mice

inferredcites →https://doi.org/10.1038/s41579-018-0036-xopenalex-snapshot

Interactions of commensal and pathogenic microorganisms with the intestinal mucosal barrier

inferredcites →https://doi.org/10.1053/j.gastro.2010.01.045openalex-snapshot

Mucin Gene Deficiency in Mice Impairs Host Resistance to an Enteric Parasitic Infection

inferredcites →https://doi.org/10.1080/19490976.2021.1966263openalex-snapshot

Deprivation of dietary fiber in specific-pathogen-free mice promotes susceptibility to the intestinal mucosal pathogen Citrobacter rodentium

inferredcites →https://doi.org/10.1084/jem.20102057openalex-snapshot

Muc5ac: a critical component mediating the rejection of enteric nematodes

inferredcites →https://doi.org/10.1093/glycob/cww134openalex-snapshot

Intestinal Muc2 mucin O-glycosylation is affected by microbiota and regulated by differential expression of glycosyltranferases

inferredcites →https://doi.org/10.1111/pim.12274openalex-snapshot

Interactions between the intestinal microbiome and helminth parasites

inferredcites →https://doi.org/10.1111/pim.1993.15.10.595openalex-snapshot

Correlations between worm burden and markers of Th1 and Th2 cell subset induction in an inbred strain of mouse infected with Trichuris muris

inferredcites →https://doi.org/10.1126/sciadv.aap7399openalex-snapshot

Manipulation of host and parasite microbiotas: Survival strategies during chronic nematode infection

inferredcites →https://doi.org/10.1126/science.1187703openalex-snapshot

Exploitation of the Intestinal Microflora by the Parasitic Nematode Trichuris muris

inferredcites →https://doi.org/10.1126/science.1188235openalex-snapshot

Adaptation via Symbiosis: Recent Spread of a Drosophila Defensive Symbiont

inferredcites →https://doi.org/10.1128/iai.00141-12openalex-snapshot

Alterations in the Porcine Colon Microbiota Induced by the Gastrointestinal Nematode Trichuris suis

inferredcites →https://doi.org/10.1128/iai.02023-14openalex-snapshot

Coinfection with an Intestinal Helminth Impairs Host Innate Immunity against Salmonella enterica Serovar Typhimurium and Exacerbates Intestinal Inflammation in Mice

inferredcites →https://doi.org/10.1128/msystems.00717-21openalex-snapshot

Dietary Modulation Alters Susceptibility to Listeria monocytogenes and Salmonella Typhimurium with or without a Gut Microbiota

inferredcites →https://doi.org/10.1146/annurev-immunol-093019-122827openalex-snapshot

Immune System Investigation Using Parasitic Helminths

inferredcites →https://doi.org/10.1186/1471-2172-9-11openalex-snapshot

IL-4/IL-13 independent goblet cell hyperplasia in experimental helminth infections

inferredcites →https://doi.org/10.1186/s12865-015-0074-3openalex-snapshot

Human helminth therapy to treat inflammatory disorders- where do we stand?

inferredcites →https://doi.org/10.1186/s40168-015-0103-8openalex-snapshot

Type 2 immunity-dependent reduction of segmented filamentous bacteria in mice infected with the helminthic parasite Nippostrongylus brasiliensis

inferredcites →https://doi.org/10.1371/journal.pntd.0000403openalex-snapshot

Immunologic Responses to Vibrio cholerae in Patients Co-Infected with Intestinal Parasites in Bangladesh

inferredcites →https://doi.org/10.1371/journal.pntd.0001856openalex-snapshot

Serine Protease(s) Secreted by the Nematode Trichuris muris Degrade the Mucus Barrier

inferredcites →https://doi.org/10.1371/journal.pntd.0005708openalex-snapshot

Chronic Trichuris muris infection causes neoplastic change in the intestine and exacerbates tumour formation in APC min/+ mice

inferredcites →https://doi.org/10.1371/journal.pone.0042248openalex-snapshot

The Goblet Cell Is the Cellular Source of the Anti-Microbial Angiogenin 4 in the Large Intestine Post Trichuris muris Infection

inferredcites →https://doi.org/10.1371/journal.pone.0044328openalex-snapshot

Fecal Lipocalin 2, a Sensitive and Broadly Dynamic Non-Invasive Biomarker for Intestinal Inflammation

inferredcites →https://doi.org/10.1371/journal.pone.0125495openalex-snapshot

Chronic Trichuris muris Infection Decreases Diversity of the Intestinal Microbiota and Concomitantly Increases the Abundance of Lactobacilli

inferredcites →https://doi.org/10.1371/journal.pone.0125945openalex-snapshot

Chronic Trichuris muris Infection in C57BL/6 Mice Causes Significant Changes in Host Microbiota and Metabolome: Effects Reversed by Pathogen Clearance

inferredcites →https://doi.org/10.1371/journal.ppat.1003000openalex-snapshot

Therapeutic Helminth Infection of Macaques with Idiopathic Chronic Diarrhea Alters the Inflammatory Signature and Mucosal Microbiota of the Colon

inferredcites →https://doi.org/10.1371/journal.ppat.1006218openalex-snapshot

Immune-driven alterations in mucin sulphation is an important mediator of Trichuris muris helminth expulsion

inferredcites →https://doi.org/10.1371/journal.ppat.1009768openalex-snapshot

Trichuris muris infection drives cell-intrinsic IL4R alpha independent colonic RELMα+ macrophages

inferredcites →https://doi.org/10.1371/journal.ppat.1011647openalex-snapshot

Bacterial contact induces polar plug disintegration to mediate whipworm egg hatching

inferredcites →https://doi.org/10.15252/emmm.202217241openalex-snapshot

Maternal diet and gut microbiome composition modulate early‐life immune development

inferredcites →https://doi.org/10.3109/08830185.2015.1096936openalex-snapshot

Interaction Between Helminths and Toll-Like Receptors: Possibilities and Potentials for Asthma Therapy

inferredcites →https://doi.org/10.3389/fcimb.2021.637570openalex-snapshot

Whipworm-Associated Intestinal Microbiome Members Consistent Across Both Human and Mouse Hosts

inferredcites →https://doi.org/10.3389/fimmu.2014.00546openalex-snapshot

Regulation of Macrophage Polarization by RON Receptor Tyrosine Kinase Signaling

inferredcites →https://doi.org/10.3389/fimmu.2020.01286openalex-snapshot

Immunity to Soil-Transmitted Helminths: Evidence From the Field and Laboratory Models

inferredcites →https://doi.org/10.3389/fimmu.2020.01604openalex-snapshot

Effectiveness of Helminth Therapy in the Prevention of Allograft Rejection: A Systematic Review of Allogeneic Transplantation

inferredcites →https://doi.org/10.3390/pathogens10080925openalex-snapshot

Trichuris muris Model: Role in Understanding Intestinal Immune Response, Inflammation and Host Defense

inferredcites →https://doi.org/10.4049/jimmunol.167.4.2234openalex-snapshot

The Role of IL-4 in Heligmosomoides polygyrus -Induced Alterations in Murine Intestinal Epithelial Cell Function

inferredcites →https://doi.org/10.4049/jimmunol.1900094openalex-snapshot

Cooperative Regulation of the Mucosal Mast Cell–Specific Protease Genes Mcpt1 and Mcpt2 by GATA and Smad Transcription Factors

inferredcites →https://doi.org/10.4049/jimmunol.1901149openalex-snapshot

Fermentable Dietary Fiber Promotes Helminth Infection and Exacerbates Host Inflammatory Responses

What points at this work

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

inferred← citeshttps://doi.org/10.1101/2025.05.09.653168openalex-snapshot

Host microbiome determines host specificity of the human whipworm, Trichuris trichiura

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