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STAT1-dependent tolerance of intestinal viral infection

https://doi.org/10.1101/2020.02.13.936252

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What this work says

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

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Characterization of PicoGreen Reagent and Development of a Fluorescence-Based Solution Assay for Double-Stranded DNA Quantitation

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Obstructive Lymphangitis Precedes Colitis in Murine Norovirus–Infected Stat1-Deficient Mice

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Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis

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Virus-Plus-Susceptibility Gene Interaction Determines Crohn's Disease Gene Atg16L1 Phenotypes in Intestine

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Cooperative Microbial Tolerance Behaviors in Host-Microbiota Mutualism

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Commensal Fungi Recapitulate the Protective Benefits of Intestinal Bacteria

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Naive CD4+ T Cell Frequency Varies for Different Epitopes and Predicts Repertoire Diversity and Response Magnitude

inferredcites →https://doi.org/10.1016/j.immuni.2012.04.011openalex-snapshot

Commensal Bacteria Calibrate the Activation Threshold of Innate Antiviral Immunity

inferredcites →https://doi.org/10.1016/j.immuni.2016.03.009openalex-snapshot

Enteric Viruses Ameliorate Gut Inflammation via Toll-like Receptor 3 and Toll-like Receptor 7-Mediated Interferon-β Production

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The dynamic influence of commensal bacteria on the immune response to pathogens

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A step-by-step guide to non-linear regression analysis of experimental data using a Microsoft Excel spreadsheet

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Fludarabine-induced immunosuppression is associated with inhibition of STAT1 signaling

inferredcites →https://doi.org/10.1038/laban0708-314openalex-snapshot

Murine norovirus, a recently discovered and highly prevalent viral agent of mice

inferredcites →https://doi.org/10.1038/nature13960openalex-snapshot

An enteric virus can replace the beneficial function of commensal bacteria

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Accounting for reciprocal host–microbiome interactions in experimental science

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Interferon-λ and interleukin 22 act synergistically for the induction of interferon-stimulated genes and control of rotavirus infection

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Type I interferon restricts type 2 immunopathology through the regulation of group 2 innate lymphoid cells

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Regulation of type I interferon responses

inferredcites →https://doi.org/10.1038/s41564-019-0416-7openalex-snapshot

Viral complementation of immunodeficiency confers protection against enteric pathogens via interferon-λ

inferredcites →https://doi.org/10.1038/s41564-019-0470-1openalex-snapshot

IFN-I and IL-22 mediate protective effects of intestinal viral infection

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Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample

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Lymphocytic choriomeningitis virus Clone 13 infection causes either persistence or acute death dependent on IFN-1, cytotoxic T lymphocytes (CTLs), and host genetics

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UCHIME improves sensitivity and speed of chimera detection

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Norovirus Triggered Microbiota-driven Mucosal Inflammation in Interleukin 10-deficient Mice

inferredcites →https://doi.org/10.1099/vir.0.059188-0openalex-snapshot

Pathology caused by persistent murine norovirus infection

inferredcites →https://doi.org/10.1126/science.1077905openalex-snapshot

STAT1-Dependent Innate Immunity to a Norwalk-Like Virus

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Blockade of Chronic Type I Interferon Signaling to Control Persistent LCMV Infection

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Persistent LCMV Infection Is Controlled by Blockade of Type I Interferon Signaling

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Helminth infection reactivates latent γ-herpesvirus via cytokine competition at a viral promoter

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Virus-helminth coinfection reveals a microbiota-independent mechanism of immunomodulation

inferredcites →https://doi.org/10.1126/science.1258025openalex-snapshot

Commensal microbes and interferon-λ determine persistence of enteric murine norovirus infection

inferredcites →https://doi.org/10.1126/science.1258100openalex-snapshot

Interferon-λ cures persistent murine norovirus infection in the absence of adaptive immunity

inferredcites →https://doi.org/10.1126/science.aaf1220openalex-snapshot

Discovery of a proteinaceous cellular receptor for a norovirus

inferredcites →https://doi.org/10.1126/science.aar3799openalex-snapshot

Tropism for tuft cells determines immune promotion of norovirus pathogenesis

inferredcites →https://doi.org/10.1128/aac.02198-15openalex-snapshot

Treatment with a Nucleoside Polymerase Inhibitor Reduces Shedding of Murine Norovirus in Stool to Undetectable Levels without Emergence of Drug-Resistant Variants

inferredcites →https://doi.org/10.1128/aem.01541-09openalex-snapshot

Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities

inferredcites →https://doi.org/10.1128/iai.66.11.5224-5231.1998openalex-snapshot

Resident Enteric Bacteria Are Necessary for Development of Spontaneous Colitis and Immune System Activation in Interleukin-10-Deficient Mice

inferredcites →https://doi.org/10.1128/jvi.00623-09openalex-snapshot

Murine Norovirus Infection Has No Significant Effect on Adaptive Immunity to Vaccinia Virus or Influenza A Virus

inferredcites →https://doi.org/10.1128/jvi.00783-07openalex-snapshot

Murine Noroviruses Comprising a Single Genogroup Exhibit Biological Diversity despite Limited Sequence Divergence

inferredcites →https://doi.org/10.1128/jvi.01445-09openalex-snapshot

Effects of Acute and Chronic Murine Norovirus Infections on Immune Responses and Recovery from Friend Retrovirus Infection

inferredcites →https://doi.org/10.1128/jvi.01864-12openalex-snapshot

A Single-Amino-Acid Change in Murine Norovirus NS1/2 Is Sufficient for Colonic Tropism and Persistence

inferredcites →https://doi.org/10.1128/jvi.03389-12openalex-snapshot

Persistent Enteric Murine Norovirus Infection Is Associated with Functionally Suboptimal Virus-Specific CD8 T Cell Responses

inferredcites →https://doi.org/10.1128/jvi.07038-11openalex-snapshot

Protruding Domain of Capsid Protein Is Necessary and Sufficient To Determine Murine Norovirus Replication and Pathogenesis In Vivo

inferredcites →https://doi.org/10.1128/jvi.07147-11openalex-snapshot

Mice Deficient in STAT1 but Not STAT2 or IRF9 Develop a Lethal CD4+T-Cell-Mediated Disease following Infection with Lymphocytic Choriomeningitis Virus

inferredcites →https://doi.org/10.1128/mspheredirect.00073-17openalex-snapshot

OptiClust, an Improved Method for Assigning Amplicon-Based Sequence Data to Operational Taxonomic Units

inferredcites →https://doi.org/10.1152/ajplung.00360.2014openalex-snapshot

Inflammatory impact of IFN-γ in CD8 + T cell-mediated lung injury is mediated by both Stat1-dependent and -independent pathways

inferredcites →https://doi.org/10.1182/blood-2005-07-2834openalex-snapshot

Modulation of STAT1 protein levels: a mechanism shaping CD8 T-cell responses in vivo

inferredcites →https://doi.org/10.1182/blood-2006-04-018929openalex-snapshot

Hypogammaglobulinemia and exacerbated CD8 T-cell–mediated immunopathology in SAP-deficient mice with chronic LCMV infection mimics human XLP disease

inferredcites →https://doi.org/10.1186/2049-2618-1-7openalex-snapshot

Murine norovirus infection does not cause major disruptions in the murine intestinal microbiota

inferredcites →https://doi.org/10.1371/journal.pone.0027310openalex-snapshot

Reducing the Effects of PCR Amplification and Sequencing Artifacts on 16S rRNA-Based Studies

inferredcites →https://doi.org/10.1371/journal.ppat.1002763openalex-snapshot

Conditional Stat1 Ablation Reveals the Importance of Interferon Signaling for Immunity to Listeria monocytogenes Infection

inferredcites →https://doi.org/10.1371/journal.ppat.1005684openalex-snapshot

Type I Interferon Receptor Deficiency in Dendritic Cells Facilitates Systemic Murine Norovirus Persistence Despite Enhanced Adaptive Immunity

inferredcites →https://doi.org/10.1371/journal.ppat.1006810openalex-snapshot

Memory CD8 T cells mediate severe immunopathology following respiratory syncytial virus infection

inferredcites →https://doi.org/10.3201/eid1410.080117openalex-snapshot

Norwalk Virus Shedding after Experimental Human Infection

inferredcites →https://doi.org/10.3354/ame01753openalex-snapshot

Minor revision to V4 region SSU rRNA 806R gene primer greatly increases detection of SAR11 bacterioplankton

inferredcites →https://doi.org/10.3389/fimmu.2016.00025openalex-snapshot

Balancing Immune Protection and Immune Pathology by CD8+ T-Cell Responses to Influenza Infection

inferredcites →https://doi.org/10.4049/jimmunol.0900995openalex-snapshot

Critical Role of IL-17RA in Immunopathology of Influenza Infection

inferredcites →https://doi.org/10.4049/jimmunol.1003009openalex-snapshot

Intrinsic IL-21 Signaling Is Critical for CD8 T Cell Survival and Memory Formation in Response to Vaccinia Viral Infection

inferredcites →https://doi.org/10.4049/jimmunol.1102062openalex-snapshot

IL-22 Mediates Host Defense against an Intestinal Intracellular Parasite in the Absence of IFN-γ at the Cost of Th17-Driven Immunopathology

inferredcites →https://doi.org/10.4049/jimmunol.1301819openalex-snapshot

NFIL3-Deficient Mice Develop Microbiota-Dependent, IL-12/23–Driven Spontaneous Colitis

inferredcites →https://doi.org/10.4049/jimmunol.1601984openalex-snapshot

STAT1 Represses Cytokine-Producing Group 2 and Group 3 Innate Lymphoid Cells during Viral Infection

inferredcites →https://doi.org/10.4049/jimmunol.180.4.2158openalex-snapshot

STAT1 Signaling in CD8 T Cells Is Required for Their Clonal Expansion and Memory Formation Following Viral Infection In Vivo

What points at this work

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

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The differences in SARS-CoV and SARS-CoV-2 specific co-expression network mediated biological process in human gut enterocytes

inferred← citeshttps://doi.org/10.1111/1348-0421.12980openalex-snapshot

Probiotics as a biotherapeutics for the management and prevention of respiratory tract diseases

inferred← citeshttps://doi.org/10.3390/molecules25214891openalex-snapshot

Probiotics in Treatment of Viral Respiratory Infections and Neuroinflammatory Disorders

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