Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Study on non-targeted metabolomics of intestinal tract of DEV- infected ducks

View through CrossRef
Abstract Introduction Duck enteritis virus (DEV) mainly causes infectious diseases characterized by intestinal hemorrhage, inflammation and parenchymal organ degeneration in ducks and other poultry. However, its mechanism of intestinal damage in ducks is not well understood. Metabolomics can provide an in-depth understanding of the full complexity of the disease. Methods In this study, 24 clinically healthy green-shell ducks (weight 1.5kg ± 20g) were randomly divided them into 2 groups (experimental group of 18 rats and control group of 6 rats). The experimental group was intramuscularly injected with 0.2 mL of DEV virus liquid (TCID50 is 3.16×10 -9 /0.1 mL), and the control group was injected with 0.2 sterilized normal saline. mL; at 66 h, 90 h and 114 h after injection (fasting for 12 h before killing), tissue samples from the duodenum and ileum were collected and analyzed by LC-MS. Results Compared with the control group, in the positive/negative mode, the metabolic pathways involved in the differential metabolites in the duodenum of DEV-infected ducks at 66h, 90h and 114h were basically the same; the metabolic pathways related to inflammatory response and immune response were tryptophan Acid metabolism, cysteine-methionine metabolism, histidine metabolism and other amino acid metabolism and fat metabolism. Among them, the metabolic pathways with more differential metabolites are amino acid biosynthesis, cysteine and methionine metabolism, tryptophan metabolism, Unsaturated fatty acid biosynthesis and purine metabolism, the metabolic pathways with more enrichment factors were IgA-related intestinal immune network pathway and lysosome pathway. Compared with the control group, there were 16 differential metabolites in the ileum tissue of DEV-infected ducks at 66 hours of infection, 52 at 90 hours of infection, and 40 at 14 hours of infection with TD114, among which the metabolic pathways with more enriched differential metabolites were Pyrimidine metabolism, tyrosine metabolism, phenylalanine metabolism and tryptophan biosynthesis, the metabolic pathways with more enrichment factors are mTOR signaling pathway, ferroptosis pathway, tryptophan metabolism pathway and caffeine metabolism pathway Conclusion The differential metabolites of DEV-infected ducks are enriched in metabolic pathways such as tryptophan metabolism, amino acid biosynthesis, cysteine-methionine metabolism, unsaturated fatty acid biosynthesis and purine metabolism, among which tryptophan metabolism pathway The enrichment is the most obvious and can be used as a follow-up study;
Title: Study on non-targeted metabolomics of intestinal tract of DEV- infected ducks
Description:
Abstract Introduction Duck enteritis virus (DEV) mainly causes infectious diseases characterized by intestinal hemorrhage, inflammation and parenchymal organ degeneration in ducks and other poultry.
However, its mechanism of intestinal damage in ducks is not well understood.
Metabolomics can provide an in-depth understanding of the full complexity of the disease.
Methods In this study, 24 clinically healthy green-shell ducks (weight 1.
5kg ± 20g) were randomly divided them into 2 groups (experimental group of 18 rats and control group of 6 rats).
The experimental group was intramuscularly injected with 0.
2 mL of DEV virus liquid (TCID50 is 3.
16×10 -9 /0.
1 mL), and the control group was injected with 0.
2 sterilized normal saline.
mL; at 66 h, 90 h and 114 h after injection (fasting for 12 h before killing), tissue samples from the duodenum and ileum were collected and analyzed by LC-MS.
Results Compared with the control group, in the positive/negative mode, the metabolic pathways involved in the differential metabolites in the duodenum of DEV-infected ducks at 66h, 90h and 114h were basically the same; the metabolic pathways related to inflammatory response and immune response were tryptophan Acid metabolism, cysteine-methionine metabolism, histidine metabolism and other amino acid metabolism and fat metabolism.
Among them, the metabolic pathways with more differential metabolites are amino acid biosynthesis, cysteine and methionine metabolism, tryptophan metabolism, Unsaturated fatty acid biosynthesis and purine metabolism, the metabolic pathways with more enrichment factors were IgA-related intestinal immune network pathway and lysosome pathway.
Compared with the control group, there were 16 differential metabolites in the ileum tissue of DEV-infected ducks at 66 hours of infection, 52 at 90 hours of infection, and 40 at 14 hours of infection with TD114, among which the metabolic pathways with more enriched differential metabolites were Pyrimidine metabolism, tyrosine metabolism, phenylalanine metabolism and tryptophan biosynthesis, the metabolic pathways with more enrichment factors are mTOR signaling pathway, ferroptosis pathway, tryptophan metabolism pathway and caffeine metabolism pathway Conclusion The differential metabolites of DEV-infected ducks are enriched in metabolic pathways such as tryptophan metabolism, amino acid biosynthesis, cysteine-methionine metabolism, unsaturated fatty acid biosynthesis and purine metabolism, among which tryptophan metabolism pathway The enrichment is the most obvious and can be used as a follow-up study;.

Related Results

Untargeted metabolomics of the intestinal tract of DEV-infected ducks
Untargeted metabolomics of the intestinal tract of DEV-infected ducks
Abstract Introduction Duck enteritis virus (DEV) mainly causes infectious diseases characterized by intestinal haemorrhage, inflammation and parench...
RNA-seq analysis of chlorogenic acid intervention in duck embryo fibroblasts infected with duck plague virus
RNA-seq analysis of chlorogenic acid intervention in duck embryo fibroblasts infected with duck plague virus
Abstract Introduction Chlorogenic acid, the primary active component in Chinese medicines like honeysuckle, exhibits anti-inflammatory and antiviral...
Summary
Summary
SummaryThe present study was performed with the aim of investigating what mechanisms are employed in eliciting the reflexly induced inhibition of intestinal motility, and thus how ...
RNA-seq analysis of chlorogenic acid intervention in duck embryo fibroblasts infected with duck plague virus
RNA-seq analysis of chlorogenic acid intervention in duck embryo fibroblasts infected with duck plague virus
Abstract Introduction Chlorogenic acid is the main active ingredient of honeysuckle, with anti-inflammatory and antiviral effects. At present, duck plague virus causes a l...
INTESTINAL FAILURE SYNDROME IN ACUTE INTESTINAL OBSTRUCTION AND WAYS OF ITS PREVENTION
INTESTINAL FAILURE SYNDROME IN ACUTE INTESTINAL OBSTRUCTION AND WAYS OF ITS PREVENTION
Abstract. Introduction. The initial manifestations of intestinal insufficiency syndrome in acute intestinal obstruction are a pronounced inhibition of intestinal motor activity, wh...
Hematopoietic Stem Cell Infected with HTLV-1 Functions As a Viral Reservoir In Vivo
Hematopoietic Stem Cell Infected with HTLV-1 Functions As a Viral Reservoir In Vivo
Abstract Human T-cell leukemia virus type 1 (HTLV-1) is a causative agent of a malignant disease of peripheral CD4+ T cells called adult T-cell leuke...
GSimp: A Gibbs sampler based left-censored missing value imputation approach for metabolomics studies
GSimp: A Gibbs sampler based left-censored missing value imputation approach for metabolomics studies
AbstractLeft-censored missing values commonly exist in targeted metabolomics datasets and can be considered as missing not at random (MNAR). Improper data processing procedures for...

Back to Top