Vomitoxin

Vomitoxin is a lipid of Prenol Lipids (PR) class. Vomitoxin is associated with abnormalities such as Infection and Gastroenteritis. The involved functions are known as mRNA Expression, Inflammation, Transcription, Genetic, Protein Biosynthesis and Adverse effects. Vomitoxin often locates in Lymphoid Tissue, Immune system, Bone Marrow and Plasma membrane. The associated genes with Vomitoxin are IMPACT gene, HIST1H1C gene and RBM39 gene. The related experimental models are Mouse Model.

Cross Reference

Introduction

To understand associated biological information of Vomitoxin, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Vomitoxin?

Vomitoxin is suspected in Infection, Gastroenteritis and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
Loading... please refresh the page if content is not showing up.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Vomitoxin

MeSH term MeSH ID Detail
Hemolysis D006461 131 associated lipids
Inflammation D007249 119 associated lipids
Body Weight D001835 333 associated lipids
Edema D004487 152 associated lipids
Esophageal Neoplasms D004938 20 associated lipids
Precancerous Conditions D011230 48 associated lipids
Stomach Neoplasms D013274 24 associated lipids
Hematuria D006417 13 associated lipids
Weight Gain D015430 101 associated lipids
Obesity D009765 29 associated lipids
Hyperplasia D006965 34 associated lipids
Carcinoma, Hepatocellular D006528 140 associated lipids
Fetal Weight D020567 12 associated lipids
Immune Complex Diseases D007105 9 associated lipids
Glomerulonephritis, IGA D005922 7 associated lipids
Swine Diseases D013553 16 associated lipids
Poultry Diseases D011201 21 associated lipids
Thymus Neoplasms D013953 15 associated lipids
Bronchopneumonia D001996 7 associated lipids
Fetal Resorption D005327 15 associated lipids
Weight Loss D015431 56 associated lipids
Anorexia D000855 8 associated lipids
Mycoses D009181 18 associated lipids
Coronavirus Infections D018352 4 associated lipids
Mycotoxicosis D015651 5 associated lipids
Adrenocortical Carcinoma D018268 4 associated lipids
Splenic Diseases D013158 5 associated lipids
Kashin-Beck Disease D057767 2 associated lipids
Ascaridiasis D001198 1 associated lipids
Per page 10 20 50 | Total 29

PubChem Associated disorders and diseases

What pathways are associated with Vomitoxin

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Vomitoxin?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
Loading... please refresh the page if content is not showing up.

What functions are associated with Vomitoxin?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Vomitoxin?

There are no associated biomedical information in the current reference collection.

What genes are associated with Vomitoxin?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Vomitoxin?

Mouse Model

Mouse Model are used in the study 'Dietary fish oil suppresses experimental immunoglobulin a nephropathy in mice.' (Pestka JJ et al., 2002).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
Loading... please refresh the page if content is not showing up.

NCBI Entrez Crosslinks

All references with Vomitoxin

Download all related citations
Per page 10 20 50 100 | Total 1588
Authors Title Published Journal PubMed Link
Girardet C et al. Central inflammation and sickness-like behavior induced by the food contaminant deoxynivalenol: a PGE2-independent mechanism. 2011 Toxicol. Sci. pmid:21873375
Wang K et al. A novel and sensitive method for the detection of deoxynivalenol in food by time-resolved fluoroimmunoassay. 2009 Toxicol. Mech. Methods pmid:19874133
Dänicke S et al. Effects of the Fusarium toxin deoxynivalenol on tissue protein synthesis in pigs. 2006 Toxicol. Lett. pmid:16814494
Tiemann U et al. The effect of feeding a diet naturally contaminated with deoxynivalenol (DON) and zearalenone (ZON) on the spleen and liver of sow and fetus from day 35 to 70 of gestation. 2008 Toxicol. Lett. pmid:18550300
Atkinson HA and Miller K Inhibitory effect of deoxynivalenol, 3-acetyldeoxynivalenol and zearalenone on induction of rat and human lymphocyte proliferation. 1984 Toxicol. Lett. pmid:6239410
Smith MC et al. Individual and combined toxicological effects of deoxynivalenol and zearalenone on human hepatocytes in in vitro chronic exposure conditions. 2017 Toxicol. Lett. pmid:28865950
Schmeits PC et al. DON shares a similar mode of action as the ribotoxic stress inducer anisomycin while TBTO shares ER stress patterns with the ER stress inducer thapsigargin based on comparative gene expression profiling in Jurkat T cells. 2014 Toxicol. Lett. pmid:24247028
Pestka JJ Deoxynivalenol-induced IgA production and IgA nephropathy-aberrant mucosal immune response with systemic repercussions. 2003 Toxicol. Lett. pmid:12676476
Larsen JC et al. Workshop on trichothecenes with a focus on DON: summary report. 2004 Toxicol. Lett. pmid:15342076
Edwards SG Influence of agricultural practices on fusarium infection of cereals and subsequent contamination of grain by trichothecene mycotoxins. 2004 Toxicol. Lett. pmid:15342078
Snijders CH Resistance in wheat to Fusarium infection and trichothecene formation. 2004 Toxicol. Lett. pmid:15342079
Hazel CM and Patel S Influence of processing on trichothecene levels. 2004 Toxicol. Lett. pmid:15342081
Pestka JJ et al. Cellular and molecular mechanisms for immune modulation by deoxynivalenol and other trichothecenes: unraveling a paradox. 2004 Toxicol. Lett. pmid:15342082
Schlatter J Toxicity data relevant for hazard characterization. 2004 Toxicol. Lett. pmid:15342084
Koch P State of the art of trichothecenes analysis. 2004 Toxicol. Lett. pmid:15342087
Schneider E et al. Rapid methods for deoxynivalenol and other trichothecenes. 2004 Toxicol. Lett. pmid:15342088
Pieters MN et al. Reduced intake of deoxynivalenol in The Netherlands: a risk assessment update. 2004 Toxicol. Lett. pmid:15342091
Visconti A et al. Reduction of deoxynivalenol during durum wheat processing and spaghetti cooking. 2004 Toxicol. Lett. pmid:15342095
Goyarts T et al. On the transfer of the Fusarium toxins deoxynivalenol (DON) and zearalenone (ZON) from sows to their fetuses during days 35-70 of gestation. 2007 Toxicol. Lett. pmid:17544604
Ndossi DG et al. An in vitro investigation of endocrine disrupting effects of trichothecenes deoxynivalenol (DON), T-2 and HT-2 toxins. 2012 Toxicol. Lett. pmid:22982764
Tryphonas H et al. Effect of deoxynivalenol (vomitoxin) on the humoral immunity of mice. 1984 Toxicol. Lett. pmid:6485014
Casteel M et al. Impact of DUSP1 on the apoptotic potential of deoxynivalenol in the epithelial cell line HepG2. 2010 Toxicol. Lett. pmid:20708668
Tutelyan VA Deoxynivalenol in cereals in Russia. 2004 Toxicol. Lett. pmid:15342094
Warth B et al. New insights into the human metabolism of the Fusarium mycotoxins deoxynivalenol and zearalenone. 2013 Toxicol. Lett. pmid:23623764
Pinton P et al. Ingestion of deoxynivalenol (DON) contaminated feed alters the pig vaccinal immune responses. 2008 Toxicol. Lett. pmid:18329193
Warth B et al. Assessment of human deoxynivalenol exposure using an LC-MS/MS based biomarker method. 2012 Toxicol. Lett. pmid:22429874
Pestka JJ et al. Altered serum immunoglobulin response to model intestinal antigens during dietary exposure to vomitoxin (deoxynivalenol). 1990 Toxicol. Lett. pmid:2296780
Van De Walle J et al. Influence of deoxynivalenol on NF-kappaB activation and IL-8 secretion in human intestinal Caco-2 cells. 2008 Toxicol. Lett. pmid:18343055
Pestka JJ et al. Immunochemical assessment of deoxynivalenol tissue distribution following oral exposure in the mouse. 2008 Toxicol. Lett. pmid:18395371
Diesing AK et al. Mycotoxin deoxynivalenol (DON) mediates biphasic cellular response in intestinal porcine epithelial cell lines IPEC-1 and IPEC-J2. 2011 Toxicol. Lett. pmid:20937367
Nagl V et al. Metabolism of the masked mycotoxin deoxynivalenol-3-glucoside in rats. 2012 Toxicol. Lett. pmid:22884771
Goyarts T and Dänicke S Bioavailability of the Fusarium toxin deoxynivalenol (DON) from naturally contaminated wheat for the pig. 2006 Toxicol. Lett. pmid:16326049
Trichothecenes with a special focus on DON. Proceedings of a workshop. September 10-12, 2003. Dublin Ireland. 2004 Toxicol. Lett. pmid:15510395
Dänicke S et al. The Fusarium toxin deoxynivalenol (DON) modulates the LPS induced acute phase reaction in pigs. 2013 Toxicol. Lett. pmid:23603058
Döll S et al. Deoxynivalenol-induced cytotoxicity, cytokines and related genes in unstimulated or lipopolysaccharide stimulated primary porcine macrophages. 2009 Toxicol. Lett. pmid:19027837
Schmeits PC et al. Assessment of the usefulness of the murine cytotoxic T cell line CTLL-2 for immunotoxicity screening by transcriptomics. 2013 Toxicol. Lett. pmid:23253260
Döll S et al. Interactions of deoxynivalenol and lipopolysaccharides on cytotoxicity protein synthesis and metabolism of DON in porcine hepatocytes and Kupffer cell enriched hepatocyte cultures. 2009 Toxicol. Lett. pmid:19477247
Fitzpatrick DW et al. Comparison of the trichothecenes deoxynivalenol and T-2 toxin for their effects on brain biogenic monoamines in the rat. 1988 Toxicol. Lett. pmid:3354008
Tryphonas H et al. Effects of deoxynivalenol (vomitoxin) on the humoral and cellular immunity of mice. 1986 Toxicol. Lett. pmid:3518157
Sergent T et al. Deoxynivalenol transport across human intestinal Caco-2 cells and its effects on cellular metabolism at realistic intestinal concentrations. 2006 Toxicol. Lett. pmid:16442754
Stanek C et al. A chronic oral exposure of pigs with deoxynivalenol partially prevents the acute effects of lipopolysaccharides on hepatic histopathology and blood clinical chemistry. 2012 Toxicol. Lett. pmid:23123154
Döll S et al. Interactions of deoxynivalenol and lipopolysaccharides on cytokine excretion and mRNA expression in porcine hepatocytes and Kupffer cell enriched hepatocyte cultures. 2009 Toxicol. Lett. pmid:19607891
Szkudelska K et al. Short-time deoxynivalenol treatment induces metabolic disturbances in the rat. 2002 Toxicol. Lett. pmid:12368054
Marzocco S et al. Pro-apoptotic effects of nivalenol and deoxynivalenol trichothecenes in J774A.1 murine macrophages. 2009 Toxicol. Lett. pmid:19410639
Flannery BM et al. Deoxynivalenol-induced weight loss in the diet-induced obese mouse is reversible and PKR-independent. 2013 Toxicol. Lett. pmid:23707852
Sugiyama K et al. Deoxynivalenol and nivalenol inhibit lipopolysaccharide-induced nitric oxide production by mouse macrophage cells. 2010 Toxicol. Lett. pmid:19857559
Bony S et al. Genotoxicity assessment of deoxynivalenol in the Caco-2 cell line model using the Comet assay. 2006 Toxicol. Lett. pmid:16828243
Li S et al. Modulation of transcription factor AP-1 activity in murine EL-4 thymoma cells by vomitoxin (deoxynivalenol). 2000 Toxicol. Appl. Pharmacol. pmid:10662601
Yang GH et al. Down-regulation of the endoplasmic reticulum chaperone GRP78/BiP by vomitoxin (Deoxynivalenol). 2000 Toxicol. Appl. Pharmacol. pmid:10652249
Wu W et al. Effects of oral exposure to naturally-occurring and synthetic deoxynivalenol congeners on proinflammatory cytokine and chemokine mRNA expression in the mouse. 2014 Toxicol. Appl. Pharmacol. pmid:24793808
Yang GH et al. Apoptosis induction by the satratoxins and other trichothecene mycotoxins: relationship to ERK, p38 MAPK, and SAPK/JNK activation. 2000 Toxicol. Appl. Pharmacol. pmid:10764628
Mishra S et al. Deoxynivalenol induced mouse skin cell proliferation and inflammation via MAPK pathway. 2014 Toxicol. Appl. Pharmacol. pmid:24937323
Pietsch C et al. Frequent biphasic cellular responses of permanent fish cell cultures to deoxynivalenol (DON). 2011 Toxicol. Appl. Pharmacol. pmid:21791220
Chung YJ et al. Transcriptional and posttranscriptional roles for p38 mitogen-activated protein kinase in upregulation of TNF-alpha expression by deoxynivalenol (vomitoxin). 2003 Toxicol. Appl. Pharmacol. pmid:14644621
Ouyang YL et al. Vomitoxin-mediated IL-2, IL-4, and IL-5 superinduction in murine CD4+ T cells stimulated with phorbol ester calcium ionophore: relation to kinetics of proliferation. 1996 Toxicol. Appl. Pharmacol. pmid:8658534
Dong W et al. Elevated gene expression and production of interleukins 2, 4, 5, and 6 during exposure to vomitoxin (deoxynivalenol) and cycloheximide in the EL-4 thymoma. 1994 Toxicol. Appl. Pharmacol. pmid:8048072
Khera KS et al. Vomitoxin (4-deoxynivalenol): effects on reproduction of mice and rats. 1984 Toxicol. Appl. Pharmacol. pmid:6740683
Moon Y et al. Hypo-responsiveness of interleukin-8 production in human embryonic epithelial intestine 407 cells independent of NF-kappaB pathway: new lessons from endotoxin and ribotoxic deoxynivalenol. 2008 Toxicol. Appl. Pharmacol. pmid:18485432
Azcona-Olivera JI et al. Induction of cytokine mRNAs in mice after oral exposure to the trichothecene vomitoxin (deoxynivalenol): relationship to toxin distribution and protein synthesis inhibition. 1995 Toxicol. Appl. Pharmacol. pmid:7597700
van Kol SW et al. The effects of deoxynivalenol on gene expression in the murine thymus. 2011 Toxicol. Appl. Pharmacol. pmid:21074547
Li S et al. Superinduction of IL-2 gene expression by vomitoxin (deoxynivalenol) involves increased mRNA stability. 1997 Toxicol. Appl. Pharmacol. pmid:9439728
Ouyang YL et al. Effects of vomitoxin (deoxynivalenol) on transcription factor NF-kappa B/Rel binding activity in murine EL-4 thymoma and primary CD4+ T cells. 1996 Toxicol. Appl. Pharmacol. pmid:8887449
Maresca M et al. Both direct and indirect effects account for the pro-inflammatory activity of enteropathogenic mycotoxins on the human intestinal epithelium: stimulation of interleukin-8 secretion, potentiation of interleukin-1beta effect and increase in the transepithelial passage of commensal bacteria. 2008 Toxicol. Appl. Pharmacol. pmid:18308354
Zhou HR et al. Differential cytokine mRNA expression in mice after oral exposure to the trichothecene vomitoxin (deoxynivalenol): dose response and time course. 1997 Toxicol. Appl. Pharmacol. pmid:9194413
Yan D et al. Role of macrophages in elevated IgA and IL-6 production by Peyer's patch cultures following acute oral vomitoxin exposure. 1998 Toxicol. Appl. Pharmacol. pmid:9473534
Bondy GS and Pestka JJ Dietary exposure to the trichothecene vomitoxin (deoxynivalenol) stimulates terminal differentiation of Peyer's patch B cells to IgA secreting plasma cells. 1991 Toxicol. Appl. Pharmacol. pmid:2020973
Katika MR et al. Transcriptome analysis of the human T lymphocyte cell line Jurkat and human peripheral blood mononuclear cells exposed to deoxynivalenol (DON): New mechanistic insights. 2012 Toxicol. Appl. Pharmacol. pmid:22846391
Islam Z et al. p38 Mitogen-activated protein kinase mediates IL-8 induction by the ribotoxin deoxynivalenol in human monocytes. 2006 Toxicol. Appl. Pharmacol. pmid:16364386
Zhou HR et al. Induction of cytokine gene expression in mice after repeated and subchronic oral exposure to vomitoxin (Deoxynivalenol): differential toxin-induced hyporesponsiveness and recovery. 1998 Toxicol. Appl. Pharmacol. pmid:9707511
Pinton P et al. The food contaminant deoxynivalenol, decreases intestinal barrier permeability and reduces claudin expression. 2009 Toxicol. Appl. Pharmacol. pmid:19289138
Islam Z et al. Endotoxin potentiation of trichothecene-induced lymphocyte apoptosis is mediated by up-regulation of glucocorticoids. 2002 Toxicol. Appl. Pharmacol. pmid:11922776
Islam Z and Pestka JJ LPS priming potentiates and prolongs proinflammatory cytokine response to the trichothecene deoxynivalenol in the mouse. 2006 Toxicol. Appl. Pharmacol. pmid:16009389
Pan X et al. Global protein phosphorylation dynamics during deoxynivalenol-induced ribotoxic stress response in the macrophage. 2013 Toxicol. Appl. Pharmacol. pmid:23352502
Choi HJ et al. HuR/ELAVL1 RNA binding protein modulates interleukin-8 induction by muco-active ribotoxin deoxynivalenol. 2009 Toxicol. Appl. Pharmacol. pmid:19591856
He K et al. Mechanisms for ribotoxin-induced ribosomal RNA cleavage. 2012 Toxicol. Appl. Pharmacol. pmid:23022514
Islam Z et al. Differential induction of glucocorticoid-dependent apoptosis in murine lymphoid subpopulations in vivo following coexposure to lipopolysaccharide and vomitoxin (deoxynivalenol). 2003 Toxicol. Appl. Pharmacol. pmid:12649039
Moon Y and Pestka JJ Cyclooxygenase-2 mediates interleukin-6 upregulation by vomitoxin (deoxynivalenol) in vitro and in vivo. 2003 Toxicol. Appl. Pharmacol. pmid:12649040
De Walle JV et al. Deoxynivalenol affects in vitro intestinal epithelial cell barrier integrity through inhibition of protein synthesis. 2010 Toxicol. Appl. Pharmacol. pmid:20362602
Alassane-Kpembi I et al. New insights into mycotoxin mixtures: the toxicity of low doses of Type B trichothecenes on intestinal epithelial cells is synergistic. 2013 Toxicol. Appl. Pharmacol. pmid:23735874
Van De Walle J et al. Physio-pathological parameters affect the activation of inflammatory pathways by deoxynivalenol in Caco-2 cells. 2010 Toxicol In Vitro pmid:20633634
Ma Y et al. A mitochondria-mediated apoptotic pathway induced by deoxynivalenol in human colon cancer cells. 2012 Toxicol In Vitro pmid:22269384
Cano-Sancho G et al. Cytotoxicity of the mycotoxins deoxynivalenol and ochratoxin A on Caco-2 cell line in presence of resveratrol. 2015 Toxicol In Vitro pmid:26100224
Seeling K et al. On the effects of Fusarium toxin contaminated wheat and wheat chaff on nutrient utilisation and turnover of deoxynivalenol and zearalenone in vitro (Rusitec). 2006 Toxicol In Vitro pmid:16321500
Devreese M et al. An in vitro model using the IPEC-J2 cell line for efficacy and drug interaction testing of mycotoxin detoxifying agents. 2013 Toxicol In Vitro pmid:23078954
Minervini F et al. Toxicity and apoptosis induced by the mycotoxins nivalenol, deoxynivalenol and fumonisin B1 in a human erythroleukemia cell line. 2004 Toxicol In Vitro pmid:14630058
Kadota T et al. Comparative study of deoxynivalenol, 3-acetyldeoxynivalenol, and 15-acetyldeoxynivalenol on intestinal transport and IL-8 secretion in the human cell line Caco-2. 2013 Toxicol In Vitro pmid:23792671
Froquet R et al. Improvement of megakaryocytic progenitor culture for toxicological investigations. 2001 Toxicol In Vitro pmid:11698171
Le Dréan G et al. Myelotoxicity of trichothecenes and apoptosis: an in vitro study on human cord blood CD34+ hematopoietic progenitor. 2005 Toxicol In Vitro pmid:15908172
Goyarts T et al. Effect of the Fusarium toxin deoxynivalenol (DON) on IgA, IgM and IgG concentrations and proliferation of porcine blood lymphocytes. 2006 Toxicol In Vitro pmid:16480848
Nasri T et al. Differential induction of apoptosis by type A and B trichothecenes in Jurkat T-lymphocytes. 2006 Toxicol In Vitro pmid:16472964
Hymery N et al. In vitro effects of trichothecenes on human dendritic cells. 2006 Toxicol In Vitro pmid:16517116
Kolf-Clauw M et al. Development of a pig jejunal explant culture for studying the gastrointestinal toxicity of the mycotoxin deoxynivalenol: histopathological analysis. 2009 Toxicol In Vitro pmid:19607908
Alm H et al. The influence of the mycotoxins deoxynivalenol and zearalenol on in vitro maturation of pig oocytes and in vitro culture of pig zygotes. 2002 Toxicol In Vitro pmid:12423645
Fink-Gremmels J [An alternative view. Mycotoxins and mycoses]. 2001 Tijdschr Diergeneeskd pmid:11285646
Cortinovis C et al. Effects of fumonisin B1 alone and combined with deoxynivalenol or zearalenone on porcine granulosa cell proliferation and steroid production. 2014 Theriogenology pmid:24576714
Schoevers EJ et al. Porcine oocytes are most vulnerable to the mycotoxin deoxynivalenol during formation of the meiotic spindle. 2010 Theriogenology pmid:20570324
Navara S and Smith KP Using near-isogenic barley lines to validate deoxynivalenol (DON) QTL previously identified through association analysis. 2014 Theor. Appl. Genet. pmid:24343199
Ansari KI et al. Retrotransposon and gene activation in wheat in response to mycotoxigenic and non-mycotoxigenic-associated Fusarium stress. 2007 Theor. Appl. Genet. pmid:17256175
Burt C et al. Mapping a Type 1 FHB resistance on chromosome 4AS of Triticum macha and deployment in combination with two Type 2 resistances. 2015 Theor. Appl. Genet. pmid:26040404
Jiang GL et al. QTL analysis of resistance to Fusarium head blight in the novel wheat germplasm CJ 9306. II. Resistance to deoxynivalenol accumulation and grain yield loss. 2007 Theor. Appl. Genet. pmid:17726598