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Central carbon metabolism is an intrinsic factor for optimal replication of a norovirus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s11684-018-0668-2openalex-snapshot
Regulation of T cell immunity by cellular metabolism
inferredcites →https://doi.org/10.1007/s12275-018-8228-7openalex-snapshot
Antiviral activity of Schizonepeta tenuifolia Briquet against noroviruses via induction of antiviral interferons
inferredcites →https://doi.org/10.1016/j.addr.2007.03.021openalex-snapshot
Modulation of host metabolism as a target of new antivirals
inferredcites →https://doi.org/10.1016/j.antiviral.2014.03.007openalex-snapshot
Triggering unfolded protein response by 2-Deoxy-d-glucose inhibits porcine epidemic diarrhea virus propagation
inferredcites →https://doi.org/10.1016/j.antiviral.2016.05.011openalex-snapshot
Inhibition of human norovirus by a viral polymerase inhibitor in the B cell culture system and in the mouse model
inferredcites →https://doi.org/10.1016/j.bbadis.2012.04.011openalex-snapshot
Herpes simplex type 1 activates glycolysis through engagement of the enzyme 6-phosphofructo-1-kinase (PFK-1)
inferredcites →https://doi.org/10.1016/j.biocel.2015.07.010openalex-snapshot
AKT mediated glycolytic shift regulates autophagy in classically activated macrophages
inferredcites →https://doi.org/10.1016/j.cell.2014.11.006openalex-snapshot
Metabolic Control of Autophagy
inferredcites →https://doi.org/10.1016/j.cell.2016.07.026openalex-snapshot
Opposing Effects of Fasting Metabolism on Tissue Tolerance in Bacterial and Viral Inflammation
inferredcites →https://doi.org/10.1016/j.cell.2017.12.025openalex-snapshot
An Integrated View of Immunometabolism
inferredcites →https://doi.org/10.1016/j.celrep.2017.04.039openalex-snapshot
Targeting Metabolic Reprogramming by Influenza Infection for Therapeutic Intervention
inferredcites →https://doi.org/10.1016/j.chom.2012.11.011openalex-snapshot
Host Metabolism Regulates Intracellular Growth of Trypanosoma cruzi
inferredcites →https://doi.org/10.1016/j.cmet.2011.11.013openalex-snapshot
Orchestration of Metabolism by Macrophages
inferredcites →https://doi.org/10.1016/j.cmet.2012.12.001openalex-snapshot
AMPK Is a Negative Regulator of the Warburg Effect and Suppresses Tumor Growth In Vivo
inferredcites →https://doi.org/10.1016/j.cmet.2014.03.009openalex-snapshot
Adenovirus E4ORF1-Induced MYC Activation Promotes Host Cell Anabolic Glucose Metabolism and Virus Replication
inferredcites →https://doi.org/10.1016/j.immuni.2015.08.023openalex-snapshot
The Cellular and Molecular Basis of Translational Immunometabolism
inferredcites →https://doi.org/10.1016/j.immuni.2017.04.013openalex-snapshot
Biochemical Underpinnings of Immune Cell Metabolic Phenotypes
inferredcites →https://doi.org/10.1016/j.immuni.2017.08.009openalex-snapshot
Foundations of Immunometabolism and Implications for Metabolic Health and Disease
inferredcites →https://doi.org/10.1016/j.it.2017.03.001openalex-snapshot
Macrophage Immunometabolism: Where Are We (Going)?
inferredcites →https://doi.org/10.1016/j.jviromet.2012.05.012openalex-snapshot
Development of a strand specific real-time RT-qPCR assay for the detection and quantitation of murine norovirus RNA
inferredcites →https://doi.org/10.1016/j.semcancer.2008.11.010openalex-snapshot
Is Akt the “Warburg kinase”?—Akt-energy metabolism interactions and oncogenesis
inferredcites →https://doi.org/10.1016/j.tim.2015.08.007openalex-snapshot
Stealing the Keys to the Kitchen: Viral Manipulation of the Host Cell Metabolic Network
inferredcites →https://doi.org/10.1016/j.virol.2006.06.006openalex-snapshot
Stable expression of a Norwalk virus RNA replicon in a human hepatoma cell line
inferredcites →https://doi.org/10.1016/j.virol.2015.02.038openalex-snapshot
Viral activation of cellular metabolism
inferredcites →https://doi.org/10.1016/j.virusres.2009.03.002openalex-snapshot
Murine norovirus-1 entry into permissive macrophages and dendritic cells is pH-independent
inferredcites →https://doi.org/10.1016/s0021-9258(18)64100-6openalex-snapshot
The Effects of 2-Deoxyglucose on the Growth and Metabolism of Cultured Human Cells
inferredcites →https://doi.org/10.1016/s0021-9258(18)64988-9openalex-snapshot
LOCALIZATION OF THE PRIMARY METABOLIC BLOCK PRODUCED BY 2-DEOXYGLUCOSE
inferredcites →https://doi.org/10.1016/s1473-3099(14)70767-4openalex-snapshot
Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis
inferredcites →https://doi.org/10.1038/emm.2016.16openalex-snapshot
AMPK activators: mechanisms of action and physiological activities
inferredcites →https://doi.org/10.1038/ijo.2008.116openalex-snapshot
AMPK: a key regulator of energy balance in the single cell and the whole organism
inferredcites →https://doi.org/10.1038/nmicrobiol.2016.246openalex-snapshot
Microbial stimulation of different Toll-like receptor signalling pathways induces diverse metabolic programmes in human monocytes
inferredcites →https://doi.org/10.1038/nprot.2015.121openalex-snapshot
Human norovirus culture in B cells
inferredcites →https://doi.org/10.1038/nri.2016.70openalex-snapshot
A guide to immunometabolism for immunologists
inferredcites →https://doi.org/10.1038/nri2448openalex-snapshot
Exploring the full spectrum of macrophage activation
inferredcites →https://doi.org/10.1038/nrm2972openalex-snapshot
The engine driving the ship: metabolic steering of cell proliferation and death
inferredcites →https://doi.org/10.1038/nrm4024openalex-snapshot
Autophagy at the crossroads of catabolism and anabolism
inferredcites →https://doi.org/10.1038/nrmicro.2016.12openalex-snapshot
Metabolic crosstalk between host and pathogen: sensing, adapting and competing
inferredcites →https://doi.org/10.1038/s41564-017-0057-7openalex-snapshot
The major targets of acute norovirus infection are immune cells in the gut-associated lymphoid tissue
inferredcites →https://doi.org/10.1038/srep27732openalex-snapshot
Six Hours after Infection, the Metabolic Changes Induced by WSSV Neutralize the Host’s Oxidative Stress Defenses
inferredcites →https://doi.org/10.1042/bst20120351openalex-snapshot
AMPK: opposing the metabolic changes in both tumour cells and inflammatory cells?
inferredcites →https://doi.org/10.1042/bst20130244openalex-snapshot
AMPK: a cellular energy sensor primarily regulated by AMP
inferredcites →https://doi.org/10.1053/gast.2002.33661openalex-snapshot
Norwalk virus binds to histo-blood group antigens present on gastroduodenal epithelial cells of secretor individuals
inferredcites →https://doi.org/10.1073/pnas.1800525115openalex-snapshot
Rhinovirus induces an anabolic reprogramming in host cell metabolism essential for viral replication
inferredcites →https://doi.org/10.1074/jbc.m113.482026openalex-snapshot
Akt Phosphorylates HK-II at Thr-473 and Increases Mitochondrial HK-II Association to Protect Cardiomyocytes
inferredcites →https://doi.org/10.1074/jbc.m805766200openalex-snapshot
Role of Xanthine Oxidase Activation and Reduced Glutathione Depletion in Rhinovirus Induction of Inflammation in Respiratory Epithelial Cells
inferredcites →https://doi.org/10.1074/jbc.r113.486464openalex-snapshot
How Metabolism Generates Signals during Innate Immunity and Inflammation
inferredcites →https://doi.org/10.1074/jbc.r115.693903openalex-snapshot
Immunometabolism: Cellular Metabolism Turns Immune Regulator
inferredcites →https://doi.org/10.1080/15384101.2015.1006971openalex-snapshot
Role of Hexokinase-1 in the survival of HIV-1-infected macrophages
inferredcites →https://doi.org/10.1083/jcb.148.2.227openalex-snapshot
The Elusive Functions of Proteoglycans
inferredcites →https://doi.org/10.1084/jem.20151570openalex-snapshot
Immunometabolism governs dendritic cell and macrophage function
inferredcites →https://doi.org/10.1091/mbc.e06-07-0593openalex-snapshot
Cytokine Stimulation Promotes Glucose Uptake via Phosphatidylinositol-3 Kinase/Akt Regulation of Glut1 Activity and Trafficking
inferredcites →https://doi.org/10.1099/vir.0.19478-0openalex-snapshot
Laboratory efforts to cultivate noroviruses
inferredcites →https://doi.org/10.1111/brv.12140openalex-snapshot
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
inferredcites →https://doi.org/10.1124/mol.63.5.1190openalex-snapshot
Release of Cellular UDP-Glucose as a Potential Extracellular Signaling Molecule
inferredcites →https://doi.org/10.1126/science.1160809openalex-snapshot
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
inferredcites →https://doi.org/10.1126/science.aaf5211openalex-snapshot
Replication of human noroviruses in stem cell–derived human enteroids
inferredcites →https://doi.org/10.1128/9781555818883.ch3openalex-snapshot
Metabolic Adaptations of Intracellullar Bacterial Pathogens and their Mammalian Host Cells during Infection (“Pathometabolism”)
inferredcites →https://doi.org/10.1128/iai.3.2.237-242.1971openalex-snapshot
Induction of Xanthine Oxidase by Virus Infections in Newborn Mice
inferredcites →https://doi.org/10.1128/jvi.00231-09openalex-snapshot
Type I and Type II Interferons Inhibit the Translation of Murine Norovirus Proteins
inferredcites →https://doi.org/10.1128/jvi.00317-16openalex-snapshot
Human Norovirus Interactions with Histo-Blood Group Antigens and Human Milk Oligosaccharides
inferredcites →https://doi.org/10.1128/jvi.00740-17openalex-snapshot
Propagation of Astrovirus VA1, a Neurotropic Human Astrovirus, in Cell Culture
inferredcites →https://doi.org/10.1128/jvi.00769-09openalex-snapshot
Hepatitis C Virus-Linked Mitochondrial Dysfunction Promotes Hypoxia-Inducible Factor 1α-Mediated Glycolytic Adaptation
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.00934-18openalex-snapshot
Rubella Viruses Shift Cellular Bioenergetics to a More Oxidative and Glycolytic Phenotype with a Strain-Specific Requirement for Glutamine
inferredcites →https://doi.org/10.1128/jvi.01824-12openalex-snapshot
Critical Role for Interferon Regulatory Factor 3 (IRF-3) and IRF-7 in Type I Interferon-Mediated Control of Murine Norovirus Replication
inferredcites →https://doi.org/10.1128/jvi.02309-14openalex-snapshot
Dengue Virus Induces and Requires Glycolysis for Optimal Replication
inferredcites →https://doi.org/10.1128/jvi.02346-05openalex-snapshot
Murine Norovirus: a Model System To Study Norovirus Biology and Pathogenesis
inferredcites →https://doi.org/10.1128/microbiolspec.mbp-0002-2014openalex-snapshot
Metabolic Adaptations of Intracellullar Bacterial Pathogens and their Mammalian Host Cells during Infection (“Pathometabolism”)
inferredcites →https://doi.org/10.1128/msphere.00374-18openalex-snapshot
Intracellular Staphylococcus aureus Modulates Host Central Carbon Metabolism To Activate Autophagy
inferredcites →https://doi.org/10.1152/ajpendo.1997.273.6.e1107openalex-snapshot
AICA riboside increases AMP-activated protein kinase, fatty acid oxidation, and glucose uptake in rat muscle
inferredcites →https://doi.org/10.1152/jappl.2000.88.6.2219openalex-snapshot
Activation of AMP-activated protein kinase increases mitochondrial enzymes in skeletal muscle
inferredcites →https://doi.org/10.1152/physiologyonline.2001.16.1.1openalex-snapshot
UTP as an Extracellular Signaling Molecule
inferredcites →https://doi.org/10.1172/jci114499openalex-snapshot
Dependence on O2- generation by xanthine oxidase of pathogenesis of influenza virus infection in mice.
inferredcites →https://doi.org/10.1186/s12864-016-3417-4openalex-snapshot
Transcriptomic analysis of human norovirus NS1-2 protein highlights a multifunctional role in murine monocytes
inferredcites →https://doi.org/10.12688/f1000research.10081.1openalex-snapshot
Recent advances in understanding noroviruses
inferredcites →https://doi.org/10.12703/p6-13openalex-snapshot
The M1 and M2 paradigm of macrophage activation: time for reassessment
inferredcites →https://doi.org/10.1371/journal.pbio.0020432openalex-snapshot
Replication of Norovirus in Cell Culture Reveals a Tropism for Dendritic Cells and Macrophages
inferredcites →https://doi.org/10.1371/journal.pmed.1001999openalex-snapshot
The Vast and Varied Global Burden of Norovirus: Prospects for Prevention and Control
inferredcites →https://doi.org/10.1371/journal.pone.0017234openalex-snapshot
2-Deoxy-D-Glucose Treatment of Endothelial Cells Induces Autophagy by Reactive Oxygen Species-Mediated Activation of the AMP-Activated Protein Kinase
inferredcites →https://doi.org/10.1371/journal.pone.0068376openalex-snapshot
HIV-1 Vpr Modulates Macrophage Metabolic Pathways: A SILAC-Based Quantitative Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0151219openalex-snapshot
Global Economic Burden of Norovirus Gastroenteritis
inferredcites →https://doi.org/10.1371/journal.ppat.1002783openalex-snapshot
Antiviral Activity of a Small Molecule Deubiquitinase Inhibitor Occurs via Induction of the Unfolded Protein Response
inferredcites →https://doi.org/10.1371/journal.ppat.1005648openalex-snapshot
An Oncogenic Virus Promotes Cell Survival and Cellular Transformation by Suppressing Glycolysis
inferredcites →https://doi.org/10.1371/journal.ppat.1006669openalex-snapshot
Pathogen manipulation of host metabolism: A common strategy for immune evasion
inferredcites →https://doi.org/10.1371/journal.ppat.1006835openalex-snapshot
Alphavirus-induced hyperactivation of PI3K/AKT directs pro-viral metabolic changes
inferredcites →https://doi.org/10.3109/08830185.2014.902452openalex-snapshot
Cellular Metabolism on T-Cell Development and Function
inferredcites →https://doi.org/10.3109/08830185.2014.969421openalex-snapshot
Cellular Metabolism and Macrophage Functional Polarization
inferredcites →https://doi.org/10.3201/eid2408.180126openalex-snapshot
Human Norovirus Replication in Human Intestinal Enteroids as Model to Evaluate Virus Inactivation
inferredcites →https://doi.org/10.3389/fimmu.2016.00630openalex-snapshot
Effects of Interferons and Viruses on Metabolism
inferredcites →https://doi.org/10.3389/fimmu.2017.00959openalex-snapshot
RNA Sequencing of Murine Norovirus-Infected Cells Reveals Transcriptional Alteration of Genes Important to Viral Recognition and Antigen Presentation
inferredcites →https://doi.org/10.3390/v10010036openalex-snapshot
Interferons: Reprogramming the Metabolic Network against Viral Infection
inferredcites →https://doi.org/10.4049/jimmunol.1600745openalex-snapshot
GM-CSF Induces Inflammatory Macrophages by Regulating Glycolysis and Lipid Metabolism
inferredcites →https://doi.org/10.4049/jimmunol.1601515openalex-snapshot
Akt Signaling Pathway in Macrophage Activation and M1/M2 Polarization
inferredcites →https://doi.org/10.7554/elife.27293openalex-snapshot
Akt regulation of glycolysis mediates bioenergetic stability in epithelial cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/jmv.70563openalex-snapshot
Viral Reprogramming of Nucleotide Synthesis and Its Impact on Viral Infection
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01152openalex-snapshot
Single Cell Metabolomics: A Future Tool to Unmask Cellular Heterogeneity and Virus-Host Interaction in Context of Emerging Viral Diseases
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